{ "id": "epg162c1rm", "slug": "2-3-sigmatropic-rearrangement", "title": "2,3-Sigmatropic rearrangement", "updated": "2026-10-21", "topic_path": [ { "id": "physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/topics/physical" }, { "id": "physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry" }, { "id": "physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods" }, { "id": "physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis" }, { "id": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis.named-preparative-methods" }, { "id": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-2-to-he", "label": "Titles 2 to He", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-2-to-he" } ], "geo": [ { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Non-geographic · 1946 to 2000: Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "path": [ { "id": "geo.nongeo", "label": "Non-geographic", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo" }, { "id": "geo.nongeo.t1946", "label": "Non-geographic · 1946 to 2000", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946" }, { "id": "geo.nongeo.t1946.physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical" }, { "id": "geo.nongeo.t1946.physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods", "label": "Named synthetic methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis.named-preparative-methods" } ] } ], "excerpt": "A 2,3-sigmatropic rearrangement is a concerted pericyclic reaction in which a sigma bond adjacent to a pi system migrates over two atoms, rearranging allylic and ylide substrates.", "snippet": "A 2,3-sigmatropic rearrangement is a concerted pericyclic reaction in which a sigma bond adjacent to a pi system migrates over two atoms, rearranging allylic and ylide substrates.", "node": "physical.chemistry.methods.chemical-synthesis.named-preparative-methods.alpha-2-to-he", "markdown": "# 2,3-Sigmatropic rearrangement\n\nA 2,3-sigmatropic rearrangement is a pericyclic reaction in which a sigma bond adjacent to a pi system migrates over two atoms of that system, converting allylic, propargylic, or onium-ylide substrates into rearranged products without changing the total number of σ- and π-bonds.[1](https://doi.org/10.1021/ja01089a050) The bracket notation records the original and terminal positions of the migrating bond. The class covers three broad substrate types: allyl and propargyl ethers, allylic N-oxides, and onium ylides.[1](https://doi.org/10.1021/ja01089a050) It differs from a [1,2]-shift such as the [1,2]-Wittig rearrangement, which proceeds through radical cleavage and recombination rather than a concerted pericyclic pathway.[2](https://doi.org/10.1021/acscentsci.6b00125)\n\n| Key fact | Detail |\n|---|---|\n| Mechanism | Concerted, thermally allowed, six-electron process through a five-membered, envelope-like transition state[1](https://doi.org/10.1021/ja01089a050) • [3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) |\n| Substrate classes | Allyl/propargyl ethers, allylic N-oxides, onium ylides[1](https://doi.org/10.1021/ja01089a050) |\n| Stereochemistry | (E)-substrates give anti products, (Z)-substrates give syn products; strong E-olefin preference in the [2,3]-Wittig series[1](https://doi.org/10.1021/ja01089a050) • [3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) |\n| Rate factor | Rate depends on the HOMO(anion)–LUMO(allyl) energy gap; the less stable the carbanion, the faster the rearrangement[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) |\n| Main competing pathway | [1,2]-Wittig or [1,2]-Stevens rearrangement; low temperature suppresses it[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) |\n| Catalytic asymmetric benchmark | Isothiourea (BTM)-catalyzed ammonium ylide rearrangement gives syn-α-amino acid derivatives with up to >95:5 dr and >99% ee[4](https://doi.org/10.1021/ja500758n) |\n| Temperature range | Reported reactions run from −80 °C to +60 °C depending on variant[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) |\n\n## How it works\n\nThe reaction is a concerted migration of the σ-bond across the termini of a π system, passing through a five-membered, envelope-like cyclic transition state in which substituents adopt pseudo-equatorial positions.[1](https://doi.org/10.1021/ja01089a050) Six electrons circulate in the cyclic array, making the thermal pathway symmetry-allowed under the [Woodward–Hoffmann rules](https://www.edgepedia.org/woodward-hoffmann-rules).[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) Doering and Roth characterized sigmatropic rearrangements as \"no-mechanism\" reactions, reflecting the absence of a discrete intermediate.[2](https://doi.org/10.1021/acscentsci.6b00125)\n\nThe envelope geometry explains the stereochemistry: (E)-substrates place substituents to give anti products and (Z)-substrates give syn products, a stereospecific relationship confirmed across the [2,3]-Wittig series.[1](https://doi.org/10.1021/ja01089a050) In catalytic asymmetric versions, stereocontrol can be imposed after ylide generation; in a BIMP-catalyzed variant the concerted rearrangement occurs preferentially from the Re-face of the anionic oxindole, directed by hydrogen bonding to the protonated catalyst.[5](https://pubs.rsc.org/en/content/articlehtml/2026/qo/d6qo00342g) Isotope effects support the concerted assignment: an inverse isotope effect shows reversible deprotonation, while a normal secondary KIE (\\( k_{\\mathrm{H}}/k_{\\mathrm{D}} = 1.19 \\)) at the allylic position marks the rearrangement itself as enantioselectivity-determining.[2](https://doi.org/10.1021/acscentsci.6b00125) Whether the ylide rearranges as a free intermediate or within a metal-bound transition state appears system-dependent: control experiments in Rh-catalyzed chemistry, in which symmetric allylic sulfides gave racemic product with chiral catalysts, support a free ylide, while calculations on a copper-catalyzed propellane system favor a copper-bound five-membered envelope transition state.[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC7894496/) • [7](https://www.nature.com/articles/s41467-025-60805-2)\n\n## How it is done\n\nYlides and carbanions are generated in two ways: deprotonation of onium salts or of ethers with a base, or reaction of an electrophilic metal-carbene or free-carbene intermediate (from metal-catalyzed or photochemical decomposition of diazo compounds) with a heteroatom nucleophile.[6](https://pmc.ncbi.nlm.nih.gov/articles/PMC7894496/)\n\nRepresentative conditions span a wide range. A catalytic enantioselective [2,3]-Wittig rearrangement uses 10 mol% cesium carbonate and 10 mol% a chiral thiourea in anhydrous cyclohexane at 10 °C for 12 h; notably, the rearrangement generally does not proceed in nonpolar solvents even after quantitative deprotonation unless a Lewis basic additive separates the tight ion pair.[2](https://doi.org/10.1021/acscentsci.6b00125) The isothiourea BTM system for allylic ammonium salts runs at −20 °C with 20 mol% HOBt, which is essential for stereocontrol, and is scalable.[4](https://doi.org/10.1021/ja500758n) BIMP organosuperbase catalysis of oxindole-derived propargylic ethers proceeds at 60 °C without stoichiometric base, giving α-allenyl alcohols in up to 98% yield and 99:1 er.[5](https://pubs.rsc.org/en/content/articlehtml/2026/qo/d6qo00342g) For the sulfoxide route, cyclic allylic alcohols are converted to allylic sulfoxides via lithium alkoxides and aryl sulfenyl chlorides, and heating the sulfoxide with a thiophile (PhS⁻ or piperidine) returns allylic alcohols in high yield.[8](https://-pubs-acs-org-443.webvpn1.xju.edu.cn/chreay/article/117/24/14201/685927/From-Allylic-Sulfoxides-to-Allylic-Sulfenates)\n\n## Origin\n\nThe term \"sigmatropic reactions\" and their orbital-symmetry selection rules were introduced by R. B. Woodward and [Roald Hoffmann](https://www.edgepedia.org/roald-hoffmann) in their 1965 [Journal of the American Chemical Society](https://www.edgepedia.org/journal-of-the-american-chemical-society) paper \"Selection Rules for Sigmatropic Reactions\".[1](https://doi.org/10.1021/ja01089a050) Their 1969 [Angewandte Chemie](https://www.edgepedia.org/angewandte-chemie) article \"The Conservation of Orbital Symmetry\" generalized the selection rules across pericyclic reactions.[9](https://doi.org/10.1002/anie.196907811) The first stereochemical study of the [2,3]-Wittig rearrangement was published by J. E. Baldwin and J. E. Patrick in the Journal of the American Chemical Society in 1971.[10](https://doi.org/10.1021/ja00743a060) W. Clark Still and Abhijit Mitra reported a highly stereoselective Z-trisubstituted-olefin variant in 1978, noting a preference for a pseudoaxially substituted transition state.[11](https://doi.org/10.1021/ja00474a049) Reinhard W. Hoffmann surveyed the stereochemistry of [2,3]-sigmatropic rearrangements in a 1979 Angewandte Chemie review.[12](https://doi.org/10.1002/anie.197905633) Takeshi Nakai and Koichi Mikami reviewed [2,3]-Wittig rearrangements in organic synthesis in Chemical Reviews in 1986.[13](https://doi.org/10.1021/cr00075a011) Andrew McNally, Brian Evans, and Matthew J. Gaunt developed an organocatalytic [2,3]-Wittig rearrangement through secondary amine catalysis, published in Angewandte Chemie in 2006.[14](https://doi.org/10.1002/anie.200504301) C. Rose Kennedy, Jennifer A. Guidera, and Eric N. Jacobsen demonstrated a synergistic ion-binding catalytic enantioselective [2,3]-Wittig rearrangement in ACS Central Science in 2016.[2](https://doi.org/10.1021/acscentsci.6b00125) Thomas H. West and colleagues reported the first catalytic asymmetric [2,3]-rearrangement of allylic ammonium ylides, using an isothiourea catalyst, in the Journal of the American Chemical Society in 2014.[4](https://doi.org/10.1021/ja500758n) Bin Xu and Uttam K. Tambar reported the first highly enantioselective [2,3]-iodonium-ylide rearrangement in Angewandte Chemie in 2017.[15](https://doi.org/10.1002/anie.201705317) V. Cere and colleagues reported ring expansion of unstabilized sulfonium ylides to eight- to ten-membered thiacycloalk-4-enes in The Journal of Organic Chemistry in 1978.[16](https://doi.org/10.1021/jo00419a024)\n\n## Variants\n\n**[2,3]-Wittig rearrangement.** Deprotonated allyl ethers rearrange to [homoallylic alcohols](https://www.edgepedia.org/homoallylic-alcohol) through the six-electron cyclic transition state; thio- analogs in which sulfur carries the migrating framework are described alongside it.[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm) • [17](https://www.organicreactions.org/pubchapter/the-23-wittig-rearrangement/) Tin–lithium exchange allows generation of extremely unstable carbanions in the [2,3]-Wittig-Still variant.[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm)\n\n**Sommelet–Hauser and Stevens rearrangements.** Ammonium ylides of benzylic type often show co-occurrence of the [1,2]-[Stevens rearrangement](https://www.edgepedia.org/stevens-rearrangement) and the [2,3]-Sommelet–Hauser rearrangement, because their activation barriers are similarly high: the [1,2] pathway proceeds by homolytic C–N scission, while the [2,3] pathway requires an unfavorable dearomatization step.[18](https://www.thieme-connect.com/products/ejournals/pdf/10.1055/a-2702-3605.pdf)\n\n**Mislow–Braverman–Evans rearrangement.** Allylic sulfoxides rearrange reversibly to allylic sulfenates, with the equilibrium generally shifted toward the sulfoxide; trapping the sulfenate with a thiophile delivers allylic alcohols under mild conditions.[8](https://-pubs-acs-org-443.webvpn1.xju.edu.cn/chreay/article/117/24/14201/685927/From-Allylic-Sulfoxides-to-Allylic-Sulfenates) Allylic sulfoxides racemize at 50–70 °C, consistent with a highly ordered concerted transition state.[8](https://-pubs-acs-org-443.webvpn1.xju.edu.cn/chreay/article/117/24/14201/685927/From-Allylic-Sulfoxides-to-Allylic-Sulfenates)\n\n**Doyle–Kirmse reaction.** An allyl sulfide reacts with a diazo compound to give a homoallyl sulfide via a sulfonium ylide.[19](http://may.chem.uh.edu/teach-files/24%20Sigmatropic%20Rearrangements_Truong%20Nguyen.pdf) In catalytic asymmetric versions of this metal-carbene chemistry, the best reported enantioselectivity is 78% ee, using methyl 1-naphthyldiazoacetate and 2-tolyl allyl sulfide with a CuBOX complex.[1](https://doi.org/10.1021/ja01089a050)\n\n## Applications\n\nThe reaction builds C–C and C–heteroatom bonds adjacent to alkenes with predictable stereochemistry. The BTM-catalyzed ammonium ylide rearrangement gives syn-α-amino acid derivatives directly from allylic ammonium salts.[4](https://doi.org/10.1021/ja500758n) BIMP catalysis of oxindole-derived propargylic ethers provides α-allenyl alcohols, and a C(3)-fluorine substituent gives stereogenic tertiary fluorides in up to 94:6 dr and 99:1 er.[5](https://pubs.rsc.org/en/content/articlehtml/2026/qo/d6qo00342g) A 2025 copper-catalyzed Doyle–Kirmse-type rearrangement using [1.1.1]propellane as carbene precursor gives allenylated or allylated methylenecyclobutanes, convertible to substituted bicyclo[2.1.1]hexanes proposed as bioisosteres of ortho- and meta-substituted benzenes.[7](https://www.nature.com/articles/s41467-025-60805-2) Dearomatizing BIMP-catalyzed rearrangements of oxindole-substituted heteroaryl ethers diverge by solvent: 1,4-dioxane gives [2,3]-products, [mesitylene](https://www.edgepedia.org/mesitylene) gives [1,2]-products, and acid treatment of [2,3]-products gives Sommelet–Hauser-type products.[20](https://research-portal.st-andrews.ac.uk/en/publications/catalytic-enantioselective-dearomatizing-23-wittig-rearrangements/) A tandem [Knoevenagel condensation](https://www.edgepedia.org/knoevenagel-condensation)–isomerization–[2,3]-rearrangement–sulfenate-trapping sequence, the SPAC condensation, gives γ-hydroxy-α,β-unsaturated derivatives.[8](https://-pubs-acs-org-443.webvpn1.xju.edu.cn/chreay/article/117/24/14201/685927/From-Allylic-Sulfoxides-to-Allylic-Sulfenates)\n\n## Limitations and alternatives\n\nThe principal competing pathway is the [1,2]-Wittig or [1,2]-Stevens rearrangement. Higher reaction temperatures favor the [1,2]-product, consistent with increasing entropy in the dissociative first step, and greater steric bulk at the ylidic or allylic terminal carbon also raises the proportion of the minor [1,2]-product.[18](https://www.thieme-connect.com/products/ejournals/pdf/10.1055/a-2702-3605.pdf) Less basic, \"naked\" ylides favor [1,2] rearrangement, whereas hydrogen-bond- or solvation-stabilized ylides favor [2,3].[18](https://www.thieme-connect.com/products/ejournals/pdf/10.1055/a-2702-3605.pdf) For the [2,3]-[Wittig reaction](https://www.edgepedia.org/wittig-reaction), low temperature is recommended to avoid contamination by the [1,2]-product.[3](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm)\n\nSubstrate structure imposes hard limits. A terminally disubstituted allylic substrate preferentially undergoes [1,2]-rearrangement at 23 °C and affords the [2,3]-product only with low conversion at reduced temperature; substrates with allylic substitution or (Z)-alkenes show very poor reactivity.[2](https://doi.org/10.1021/acscentsci.6b00125) In the BIMP allylic series, (E)-ethers rearrange effectively while (Z)-ethers react slowly, so the process is stereoselective but not stereospecific there.[5](https://pubs.rsc.org/en/content/articlehtml/2026/qo/d6qo00342g) In the BTM ammonium ylide system, an N-allyl rather than N-cinnamyl unit gives only 56% ee, so an aryl or vinyl unit is required for high enantioselectivity, and generation and isolation of the reactive ammonium salts remains difficult.[4](https://doi.org/10.1021/ja500758n) Catalytic asymmetric [2,3]-Wittig rearrangements remain scarce because strong bases are typically required.[1](https://doi.org/10.1021/ja01089a050)\n\nThe [1,2]/[2,3] competition has been reframed by recent mechanistic work. In Singleton's analysis, both rearrangements pass through the same transition state at a secondary saddle point and diverge at a valley-ridge inflection.[18](https://www.thieme-connect.com/products/ejournals/pdf/10.1055/a-2702-3605.pdf) Consistently, [1,2]-Wittig products of allylic ethers have been shown to arise from a cascade beginning with an enantioselective BIMP-catalyzed [2,3]-rearrangement followed by an enantioretentive fragmentation–recombination, formally equivalent to a Woodward–Hoffmann-forbidden thermal [1,3]-shift; Hammett analysis (\\( \\rho = +0.76 \\)), absence of spin density, and no locatable concerted [1,3] transition state support an ionic mechanism.[21](https://www.nature.com/articles/s41557-025-02022-4)\n\n## References\n\n1. [R. B. Woodward, Roald Hoffmann (1965). Selection Rules for Sigmatropic Reactions. Journal of the American Chemical Society.](https://doi.org/10.1021/ja01089a050)\n2. [C. Rose Kennedy, Jennifer A. Guidera, Eric N. Jacobsen (2016). Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement. ACS Central Science.](https://doi.org/10.1021/acscentsci.6b00125)\n3. [[2,3]-Wittig Rearrangement (organic-chemistry.org named reactions)](https://www.organic-chemistry.org/namedreactions/2,3-wittig-rearrangement.shtm)\n4. [Thomas H. West and colleagues (2014). An Isothiourea-Catalyzed Asymmetric [2,3]-Rearrangement of Allylic Ammonium Ylides. Journal of the American Chemical Society.](https://doi.org/10.1021/ja500758n)\n5. [Enantioselective BIMP-catalysed [2,3]-Wittig rearrangements of oxindole-derived allylic and propargylic ethers](https://pubs.rsc.org/en/content/articlehtml/2026/qo/d6qo00342g)\n6. [Recent Perspectives on Rearrangement Reactions of Ylides via Carbene Transfer Reactions](https://pmc.ncbi.nlm.nih.gov/articles/PMC7894496/)\n7. [[2,3]-Sigmatropic rearrangement with [1.1.1]propellane | Nature Communications](https://www.nature.com/articles/s41467-025-60805-2)\n8. [From Allylic Sulfoxides to Allylic Sulfenates: Fifty Years of a Never-Ending [2,3]-Sigmatropic Rearrangement (Chemical Reviews, ACS)](https://-pubs-acs-org-443.webvpn1.xju.edu.cn/chreay/article/117/24/14201/685927/From-Allylic-Sulfoxides-to-Allylic-Sulfenates)\n9. [R. B. Woodward, Roald Hoffmann (1969). The Conservation of Orbital Symmetry. Angewandte Chemie International Edition in English.](https://doi.org/10.1002/anie.196907811)\n10. [J. E. Baldwin, J. E. Patrick (1971). Stereochemistry of [2,3]-sigmatropic reactions. Wittig rearrangement. Journal of the American Chemical Society.](https://doi.org/10.1021/ja00743a060)\n11. [W. Clark Still, Abhijit Mitra (1978). A highly stereoselective synthesis of Z-trisubstituted olefins via [2,3]-sigmatropic rearrangement. Preference for a pseudoaxially substituted transition state. Journal of the American Chemical Society.](https://doi.org/10.1021/ja00474a049)\n12. [Reinhard W. Hoffmann (1979). Stereochemistry of [2,3]Sigmatropic Rearrangements. Angewandte Chemie International Edition in English.](https://doi.org/10.1002/anie.197905633)\n13. [Takeshi Nakai, Koichi Mikami (1986). [2,3]-Wittig sigmatropic rearrangements in organic synthesis. Chemical Reviews.](https://doi.org/10.1021/cr00075a011)\n14. [Andrew McNally, Brian Evans, Matthew J. Gaunt (2006). Organocatalytic Sigmatropic Reactions: Development of a [2,3] Wittig Rearrangement through Secondary Amine Catalysis. Angewandte Chemie International Edition.](https://doi.org/10.1002/anie.200504301)\n15. [Bin Xu, Uttam K. Tambar (2017). Copper‐Catalyzed Enantio‐, Diastereo‐, and Regioselective [2,3]‐Rearrangements of Iodonium Ylides. Angewandte Chemie International Edition.](https://doi.org/10.1002/anie.201705317)\n16. [V. Cere and colleagues (1978). Ring expansion by 2,3-sigmatropic shifts of unstabilized sulfonium ylides. Synthesis of eight- to ten-membered thiacycloalk-4-enes. The Journal of Organic Chemistry.](https://doi.org/10.1021/jo00419a024)\n17. [The [2,3]-Wittig Rearrangement (Organic Reactions, Vol. 46, Nakai & Mikami, 1994)](https://www.organicreactions.org/pubchapter/the-23-wittig-rearrangement/)\n18. [Ammonium ylides: [2,3]- vs [1,2]-sigmatropic rearrangement competition (Thieme, 10.1055/a-2702-3605)](https://www.thieme-connect.com/products/ejournals/pdf/10.1055/a-2702-3605.pdf)\n19. [Sigmatropic Rearrangements (lecture notes, University of Houston)](http://may.chem.uh.edu/teach-files/24%20Sigmatropic%20Rearrangements_Truong%20Nguyen.pdf)\n20. [Catalytic enantioselective dearomatizing [2,3]-Wittig rearrangements allow divergent [2,3]-, [1,2]- and Sommelet–Hauser type products (JACS, e-pub 25 May 2026)](https://research-portal.st-andrews.ac.uk/en/publications/catalytic-enantioselective-dearomatizing-23-wittig-rearrangements/)\n21. [The catalytic enantioselective [1,2]-Wittig rearrangement cascade of allylic ethers | Nature Chemistry](https://www.nature.com/articles/s41557-025-02022-4)\n\n---\n*Topic: Encyclopedia › Physical world and mathematics › Chemistry › Chemical principles and methods › Chemical synthesis › Named synthetic methods › Titles 2 to He*\n\n*Initially written Sep 29, 2026 · Edited: Oct 15, 2026; Oct 21, 2026*\n\n*Copyright 2026 EdgeChat AI, a subsidiary of Biostate AI.*\n\nLicense: Edgepedia Community License 1.0, https://www.edgepedia.org/edgepedia/license\n", "same_as": [], "url": "https://www.edgepedia.org/2-3-sigmatropic-rearrangement", "markdown_url": "https://www.edgepedia.org/2-3-sigmatropic-rearrangement.md", "license": { "name": "Edgepedia Community License 1.0", "url": "https://www.edgepedia.org/edgepedia/license", "summary": "Free with credit, commercial use included. AI training is open to everyone. For other uses, organizations over USD 100M in revenue or 100M monthly users license separately.", "spdx": "LicenseRef-Edgepedia-Community-1.0" }, "credit": "\"2,3-Sigmatropic rearrangement\", Edgepedia (EdgeChat), https://www.edgepedia.org/2-3-sigmatropic-rearrangement. Edgepedia Community License 1.0.", "credit_md": "\"[2,3-Sigmatropic rearrangement](https://www.edgepedia.org/2-3-sigmatropic-rearrangement)\", Edgepedia (EdgeChat), [https://www.edgepedia.org/2-3-sigmatropic-rearrangement](https://www.edgepedia.org/2-3-sigmatropic-rearrangement). [Edgepedia Community License 1.0](https://www.edgepedia.org/edgepedia/license).", "credit_html": "\"2,3-Sigmatropic rearrangement\", Edgepedia (EdgeChat), https://www.edgepedia.org/2-3-sigmatropic-rearrangement. Edgepedia Community License 1.0.", "speakable": "A 2,3-sigmatropic rearrangement is a concerted pericyclic reaction in which a sigma bond adjacent to a pi system migrates over two atoms, rearranging allylic and ylide substrates." }