甲亚胺叶立德与烯烃的催化对映选择性1,3-偶极环加成反应：制备对映体富集的高取代脯氨酸衍生物的直接策略。 - Suppr

Suppr

超能文献

Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives.

作者信息

Nájera Carmen, Sansano José M

机构信息

Departamento de Química Orgánica, Universidad de Alicante, Apartado 99, 03080 Alicante, Spain.

出版信息

Angew Chem Int Ed Engl. 2005 Oct 7;44(39):6272-6. doi: 10.1002/anie.200501074.

DOI:10.1002/anie.200501074

PMID:16172996

Abstract

摘要

相似文献

Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives.

Angew Chem Int Ed Engl. 2005 Oct 7;44(39):6272-6. doi: 10.1002/anie.200501074.

Highly enantioselective asymmetric 1,3-dipolar cycloaddition of azomethine ylide catalyzed by a copper(I)/ClickFerrophos complex.

Org Lett. 2008 May 1;10(9):1747-50. doi: 10.1021/ol8003996. Epub 2008 Mar 29.

Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3-allenoate dipolarophiles.

Org Lett. 2009 Nov 5;11(21):4946-9. doi: 10.1021/ol9020964.

Enantioselective copper-catalyzed 1,3-dipolar cycloadditions.

Chem Rev. 2008 Aug;108(8):2887-902. doi: 10.1021/cr078371m. Epub 2008 Jul 10.

Catalytic asymmetric 1,3-dipolar cycloaddition reactions of azomethine ylides-a simple approach to optically active highly functionalized proline derivatives.

Angew Chem Int Ed Engl. 2002 Nov 15;41(22):4236-8. doi: 10.1002/1521-3773(20021115)41:22<4236::AID-ANIE4236>3.0.CO;2-W.

A convenient procedure for the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and alkenes.

Org Lett. 2005 Oct 13;7(21):4569-72. doi: 10.1021/ol0514653.

Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Org Lett. 2005 Sep 15;7(19):4241-4. doi: 10.1021/ol0516925.

The phenylsulfonyl group as a temporal regiochemical controller in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides.

Angew Chem Int Ed Engl. 2009;48(2):340-3. doi: 10.1002/anie.200805063.

Highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides catalyzed by copper(I)/TF-BiphamPhos complexes.

J Am Chem Soc. 2008 Dec 24;130(51):17250-1. doi: 10.1021/ja807669q.

Catalytic enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and alkenes by using phosphoramidite-silver(I) complexes.

Angew Chem Int Ed Engl. 2008;47(32):6055-8. doi: 10.1002/anie.200801690.

引用本文的文献

Mechanistic insights into the (3 + 2) cycloaddition of azomethine ylide with dimethyl acetylenedicarboxylate bond evolution theory.

RSC Adv. 2025 Aug 21;15(36):29666-29679. doi: 10.1039/d5ra04992j. eCollection 2025 Aug 18.

Synthesis of xanthenone fused spiro pyrrolidine oxindoles via multicomponent [3 + 2] cycloaddition reactions.

Mol Divers. 2025 Mar 21. doi: 10.1007/s11030-025-11167-w.

Electron-rich benzofulvenes as effective dipolarophiles in copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides.

Chem Sci. 2023 Apr 25;14(20):5460-5469. doi: 10.1039/d3sc00435j. eCollection 2023 May 24.

Recent Development of Bis-Cyclometalated Chiral-at-Iridium and Rhodium Complexes for Asymmetric Catalysis.

ACS Org Inorg Au. 2021 Dec 3;2(2):99-125. doi: 10.1021/acsorginorgau.1c00032. eCollection 2022 Apr 6.

Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides.

RSC Adv. 2020 Mar 10;10(17):10263-10276. doi: 10.1039/c9ra10463a. eCollection 2020 Mar 6.

Predicting Absolute Rate Constants for Huisgen Reactions of Unsaturated Iminium Ions with Diazoalkanes.

Angew Chem Int Ed Engl. 2020 Jul 20;59(30):12527-12533. doi: 10.1002/anie.202003029. Epub 2020 May 11.

Kinetic Resolution of Alkylidene Norcamphors via a Ligand-Controlled Umpolung-Type 1,3-Dipolar Cycloaddition.

iScience. 2019 Jan 25;11:146-159. doi: 10.1016/j.isci.2018.12.010. Epub 2018 Dec 15.

1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives.

Molecules. 2016 Jul 23;21(8):935. doi: 10.3390/molecules21080935.

A new entry to azomethine ylides from allylic amines and glyoxals: shifting the reliance on amino ester precursors.

Org Lett. 2014 Oct 3;16(19):4996-9. doi: 10.1021/ol5022614. Epub 2014 Sep 23.

Copper-phenanthroline catalysts for regioselective synthesis of pyrrolo[3',4':3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and of pyrrolo[1,2-a]phenanthrolines under mild conditions.

Beilstein J Org Chem. 2014 Mar 20;10:692-700. doi: 10.3762/bjoc.10.62. eCollection 2014.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives.

作者信息

Nájera Carmen, Sansano José M

机构信息

Departamento de Química Orgánica, Universidad de Alicante, Apartado 99, 03080 Alicante, Spain.

出版信息

Angew Chem Int Ed Engl. 2005 Oct 7;44(39):6272-6. doi: 10.1002/anie.200501074.

DOI:10.1002/anie.200501074

PMID:16172996

Abstract

摘要

相似文献

Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives.

Angew Chem Int Ed Engl. 2005 Oct 7;44(39):6272-6. doi: 10.1002/anie.200501074.

Highly enantioselective asymmetric 1,3-dipolar cycloaddition of azomethine ylide catalyzed by a copper(I)/ClickFerrophos complex.

Org Lett. 2008 May 1;10(9):1747-50. doi: 10.1021/ol8003996. Epub 2008 Mar 29.

Highly enantioselective catalytic 1,3-dipolar cycloaddition involving 2,3-allenoate dipolarophiles.

Org Lett. 2009 Nov 5;11(21):4946-9. doi: 10.1021/ol9020964.

Enantioselective copper-catalyzed 1,3-dipolar cycloadditions.

Chem Rev. 2008 Aug;108(8):2887-902. doi: 10.1021/cr078371m. Epub 2008 Jul 10.

Catalytic asymmetric 1,3-dipolar cycloaddition reactions of azomethine ylides-a simple approach to optically active highly functionalized proline derivatives.

Angew Chem Int Ed Engl. 2002 Nov 15;41(22):4236-8. doi: 10.1002/1521-3773(20021115)41:22<4236::AID-ANIE4236>3.0.CO;2-W.

A convenient procedure for the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and alkenes.

Org Lett. 2005 Oct 13;7(21):4569-72. doi: 10.1021/ol0514653.

Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Org Lett. 2005 Sep 15;7(19):4241-4. doi: 10.1021/ol0516925.

The phenylsulfonyl group as a temporal regiochemical controller in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides.

Angew Chem Int Ed Engl. 2009;48(2):340-3. doi: 10.1002/anie.200805063.

Highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides catalyzed by copper(I)/TF-BiphamPhos complexes.

J Am Chem Soc. 2008 Dec 24;130(51):17250-1. doi: 10.1021/ja807669q.

Catalytic enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and alkenes by using phosphoramidite-silver(I) complexes.

Angew Chem Int Ed Engl. 2008;47(32):6055-8. doi: 10.1002/anie.200801690.

引用本文的文献

Mechanistic insights into the (3 + 2) cycloaddition of azomethine ylide with dimethyl acetylenedicarboxylate bond evolution theory.

RSC Adv. 2025 Aug 21;15(36):29666-29679. doi: 10.1039/d5ra04992j. eCollection 2025 Aug 18.

Synthesis of xanthenone fused spiro pyrrolidine oxindoles via multicomponent [3 + 2] cycloaddition reactions.

Mol Divers. 2025 Mar 21. doi: 10.1007/s11030-025-11167-w.

Electron-rich benzofulvenes as effective dipolarophiles in copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides.

Chem Sci. 2023 Apr 25;14(20):5460-5469. doi: 10.1039/d3sc00435j. eCollection 2023 May 24.

Recent Development of Bis-Cyclometalated Chiral-at-Iridium and Rhodium Complexes for Asymmetric Catalysis.

ACS Org Inorg Au. 2021 Dec 3;2(2):99-125. doi: 10.1021/acsorginorgau.1c00032. eCollection 2022 Apr 6.

Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides.

RSC Adv. 2020 Mar 10;10(17):10263-10276. doi: 10.1039/c9ra10463a. eCollection 2020 Mar 6.

Predicting Absolute Rate Constants for Huisgen Reactions of Unsaturated Iminium Ions with Diazoalkanes.

Angew Chem Int Ed Engl. 2020 Jul 20;59(30):12527-12533. doi: 10.1002/anie.202003029. Epub 2020 May 11.

Kinetic Resolution of Alkylidene Norcamphors via a Ligand-Controlled Umpolung-Type 1,3-Dipolar Cycloaddition.

iScience. 2019 Jan 25;11:146-159. doi: 10.1016/j.isci.2018.12.010. Epub 2018 Dec 15.

1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives.

Molecules. 2016 Jul 23;21(8):935. doi: 10.3390/molecules21080935.

A new entry to azomethine ylides from allylic amines and glyoxals: shifting the reliance on amino ester precursors.

Org Lett. 2014 Oct 3;16(19):4996-9. doi: 10.1021/ol5022614. Epub 2014 Sep 23.

Copper-phenanthroline catalysts for regioselective synthesis of pyrrolo[3',4':3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and of pyrrolo[1,2-a]phenanthrolines under mild conditions.

Beilstein J Org Chem. 2014 Mar 20;10:692-700. doi: 10.3762/bjoc.10.62. eCollection 2014.