Research graph
References from Copper-Catalyzed 1,3-Propargyl Shift: Development of an Anionic Rearrangement of <i>ortho</i> -Metalated Aryl Propargyl Ethers. Local targets link to admitted publications; unresolved targets remain external evidence.
The [1,3] O-to-C rearrangement: opportunities for stereoselective synthesis
10.1039/b714881j · 2008 · External reference
Recent advances in metal-catalyzed asymmetric sigmatropic rearrangements
10.1039/d2sc03806d · 2022 · External reference
Recent advances in catalytic asymmetric [1,3]-rearrangement reactions
10.1039/d2qo01027e · 2022 · External reference
Copper-Catalyzed Enantioselective [1,2] O-to-C Rearrangement of Heteroaryl Alkyl Ethers
10.1021/acs.orglett.5c05160 · 2026 · External reference
Claisen Rearrangement over the Past Nine Decades
10.1021/cr020703u · 2004 · External reference
Catalysis of the Claisen rearrangement
10.1016/j.tet.2007.10.079 · 2008 · External reference
Claisen Rearrangement of Aliphatic Allyl Vinyl Ethers from 1912 to 2012:100 Years of Electrophilic Catalysis
10.1055/s-0032-1316869 · 2013 · External reference
Application of Claisen Rearrangement and Olefin Metathesis in Organic Synthesis
10.1002/asia.201800613 · 2018 · External reference
Claisen Rearrangement of Benzyl Vinyl Ehters and Heterobenzyl Vinyl Ethers
10.1055/s-0036-1589529 · 2018 · External reference
[2,3]-Wittig Sigmatropic Rearrangement in Organic Synthesis
10.1021/cr00075a011 · 1986 · External reference
Stereochemistry of [2,3]Sigmatropic Rearrangements
10.1002/anie.197905633 · 1979 · External reference
Acyclic Stereocontrol via [2,3]-Wittig Sigmatropic Rearrangement
10.1055/s-1991-26523 · 1991 · External reference
Asymmetric [2,3]-Wittig rearrangement as a general tool for asymmetric synthesis
10.1351/pac199769030595 · 1997 · External reference
Recent advances in the Overman rearrangement: synthesis of natural products and valuable compounds
10.1039/c6ob02625g · 2017 · External reference
The Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates – Recent Advances
10.1002/ejoc.201301033 · 2014 · External reference
[3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products
10.1039/b901177n · 2009 · External reference
The [1,2]- and [1,4]-Wittig rearrangement
10.1016/j.tet.2019.130857 · 2020 · External reference
Wittig Rearrangement of Lithiated Allyl Aryl Ethers: A Mechanistic Study
10.1002/ejoc.200600304 · 2006 · External reference
The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics
10.1039/c8cs00830b · 2019 · External reference
Propargyl Claisen rearrangement: allene synthesis and beyond
10.1039/c2cs35311c · 2013 · External reference
Regio- and Stereoselective Copper-induced Isomerization of 2-Alkenyl 2-Lithiophenyl Ethers to 2-(2-Alkenyl)phenols
10.1016/s0040-4039(97)01379-8 · 1997 · External reference
Synthesis of Polysubstituted Naphthofurans and Indenofurans Based on a Regiodivergent Intramolecular Carbometalation Strategy with 2-(2’-Alkynylaryl)-3-iodofurans
10.1002/chem.202300132 · 2023 · External reference
Investigating chemical diversity: o-propargylphenols as key compounds in the divergent synthesis of 2-substituted benzofurans and chromenes
10.1039/d4ob01272k · 2024 · External reference
The Anionic Phospho-Fries Rearrangement
10.2174/1385272043370717 · 2004 · External reference
Stereochemistry of [2,3]Sigmatropic Rearrangements
10.1002/anie.197905633 · ExternalCitation · doi-reference
Application of Claisen Rearrangement and Olefin Metathesis in Organic Synthesis
10.1002/asia.201800613 · ExternalCitation · doi-reference
Synthesis of Polysubstituted Naphthofurans and Indenofurans Based on a Regiodivergent Intramolecular Carbometalation Strategy with 2-(2’-Alkynylaryl)-3-iodofurans
10.1002/chem.202300132 · ExternalCitation · doi-reference
Wittig Rearrangement of Lithiated Allyl Aryl Ethers: A Mechanistic Study
10.1002/ejoc.200600304 · ExternalCitation · doi-reference
The Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates – Recent Advances
10.1002/ejoc.201301033 · ExternalCitation · doi-reference
Catalysis of the Claisen rearrangement
10.1016/j.tet.2007.10.079 · ExternalCitation · doi-reference
The [1,2]- and [1,4]-Wittig rearrangement
10.1016/j.tet.2019.130857 · ExternalCitation · doi-reference
Regio- and Stereoselective Copper-induced Isomerization of 2-Alkenyl 2-Lithiophenyl Ethers to 2-(2-Alkenyl)phenols
10.1016/s0040-4039(97)01379-8 · ExternalCitation · doi-reference
Copper-Catalyzed Enantioselective [1,2] O-to-C Rearrangement of Heteroaryl Alkyl Ethers
10.1021/acs.orglett.5c05160 · ExternalCitation · doi-reference
[2,3]-Wittig Sigmatropic Rearrangement in Organic Synthesis
10.1021/cr00075a011 · ExternalCitation · doi-reference
Claisen Rearrangement over the Past Nine Decades
10.1021/cr020703u · ExternalCitation · doi-reference
The [1,3] O-to-C rearrangement: opportunities for stereoselective synthesis
10.1039/b714881j · ExternalCitation · doi-reference
[3,3]-Sigmatropic rearrangements: recent applications in the total synthesis of natural products
10.1039/b901177n · ExternalCitation · doi-reference
Propargyl Claisen rearrangement: allene synthesis and beyond
10.1039/c2cs35311c · ExternalCitation · doi-reference
Recent advances in the Overman rearrangement: synthesis of natural products and valuable compounds
10.1039/c6ob02625g · ExternalCitation · doi-reference
The anionic Fries rearrangement: a convenient route to ortho-functionalized aromatics
10.1039/c8cs00830b · ExternalCitation · doi-reference
Recent advances in catalytic asymmetric [1,3]-rearrangement reactions
10.1039/d2qo01027e · ExternalCitation · doi-reference
Recent advances in metal-catalyzed asymmetric sigmatropic rearrangements
10.1039/d2sc03806d · ExternalCitation · doi-reference
Investigating chemical diversity: o-propargylphenols as key compounds in the divergent synthesis of 2-substituted benzofurans and chromenes
10.1039/d4ob01272k · ExternalCitation · doi-reference
Claisen Rearrangement of Aliphatic Allyl Vinyl Ethers from 1912 to 2012:100 Years of Electrophilic Catalysis
10.1055/s-0032-1316869 · ExternalCitation · doi-reference
Claisen Rearrangement of Benzyl Vinyl Ehters and Heterobenzyl Vinyl Ethers
10.1055/s-0036-1589529 · ExternalCitation · doi-reference
Acyclic Stereocontrol via [2,3]-Wittig Sigmatropic Rearrangement
10.1055/s-1991-26523 · ExternalCitation · doi-reference
Asymmetric [2,3]-Wittig rearrangement as a general tool for asymmetric synthesis
10.1351/pac199769030595 · ExternalCitation · doi-reference
The Anionic Phospho-Fries Rearrangement
10.2174/1385272043370717 · ExternalCitation · doi-reference
