Highly stereoselective synthesis of β,γ-disubstituted and α,β,γ-trisubstituted butyrolactones-Reference-Cited by-同舟云学术

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Highly stereoselective synthesis of β,γ-disubstituted and α,β,γ-trisubstituted butyrolactones

Published:2008-11 Issue:45 Volume:64 Page:10331-10338
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Wu Xiaoyu,Cao Weiguo,Zhang Hui,Chen Jie,Jiang Haiyan,Deng Hongmei,Shao Min,Zhang Jiaping,Chen Huiyun

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference58 articles.

1. Synthesis and Biological Activity of ?-Methylene-?-butyrolactones

2. Lignans;Ayres,1990

3. Chemistry & Pharmacology of Natural Products. Lignans, Chemical, Biological and Clinical Properties;Ayreas,1990

4. Phytochemical Potential of Tropical Plants;Cava,1993

5. Enantiomerically Pure γ-Butyrolactones in Natural Products Synthesis;Koch,1995

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1. Cloke–Wilson rearrangement: a unique gateway to access five-membered heterocycles;RSC Advances;2023

2. The Cloke–Wilson rearrangement of aroyl-substituted donor–acceptor cylopropanes containing arylethyl donors;Organic & Biomolecular Chemistry;2022

3. Synthesis of disubstituted γ-butyrolactones and spirocyclopropanes via a multicomponent reaction of aldehydes, Meldrum's acid and sulfoxonium ylides;Organic Chemistry Frontiers;2021

4. Enantioselective Ammonium Ylide Mediated One‐Pot Synthesis of Highly Substituted γ ‐Butyrolactones;Advanced Synthesis & Catalysis;2020-04-17

5. Stereoselective Sequential Spirocyclopropanation/Cloke–Wilson Rearrangement Reactions for Synthesis of trans-β,γ-Disubstituted γ-Butyrolactones Using Alkylidene Meldrum’s Acid and Benzyl Halides;The Journal of Organic Chemistry;2020-01-10

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