Nouvelle cyclopentannélation regiosélective par une séquence tandem ouverture electrophile/cycloaddition [3+2] entre cétones méthylènecyclopropaniques et l'allyltriméthylsilane-Reference-Cited by-同舟云学术

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Nouvelle cyclopentannélation regiosélective par une séquence tandem ouverture electrophile/cycloaddition [3+2] entre cétones méthylènecyclopropaniques et l'allyltriméthylsilane

Published:1998-06 Issue:24 Volume:54 Page:6725-6738
ISSN:0040-4020
Container-title:Tetrahedron
language:fr
Short-container-title:Tetrahedron

Author:

Monti Honoré,Rizzotto Denis,Léandri Gilbert

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference110 articles.

1. Cyclopentanoïd Terpene Derivatives,1969

2. Dictionary of Natural Products,1992

3. Centenary Lecture. Cyclopentanoids: a challenge for new methodology

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Carbocycles from donor–acceptor cyclopropanes;Organic & Biomolecular Chemistry;2015

2. ChemInform Abstract: Novel Regioselective Cyclopentanellation via Tandem Electrophilic Ring Opening-[3 + 2]Cycloaddition Between Methylenecyclopropane Ketones and Allyltrimethylsilane;ChemInform;2010-06-20

3. HOTf-Catalyzed Rearrangement of Methylenecyclopropane Aryl and Alkyl Alcohols;European Journal of Organic Chemistry;2010-05-31

4. A Highly Site-, Regio-, and Stereoselective Lewis Acid Catalyzed Formal [3+3] Cycloaddition of Methylenecyclopropane-1,1-Diesters with C,N-Diarylnitrones;Chemistry - A European Journal;2008-11-25

5. Lewis Acid Catalyzed Ring-Opening Intramolecular Friedel−Crafts Alkylation of Methylenecyclopropane 1,1-Diesters;Organic Letters;2008-11-08

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