An unprecedented outcome of the lithium–ammonia reduction of enones: the formation of cyclopropanols-Reference-Cited by-同舟云学术

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An unprecedented outcome of the lithium–ammonia reduction of enones: the formation of cyclopropanols

Published:2002-12 Issue:52 Volume:43 Page:9649-9652
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Dumas Françoise,Thominiaux Cyrille,Miet Christine,d'Angelo Jean,Desmaële Didier,Nour Mohammed,Cavé Christian,Morgant Georges,Tran Huu-Dau Marie-Elise

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. The Stereochemistry of the Lithium-Ammonia Reduction of α,β-Unsaturated Ketones

2. Condensation of formaldehyde with regiospecifically generated anions

3. Symmetrically-substituted decalin-based scaffolds

4. Synthesis of unsaturated carbonyl compounds via a chromium-mediated allylic oxidation by 70% tert.butylhydroperoxide

5. Structure relation of conjugated cycloalkenones and their ketals

Cited by 3 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. Allylic Oxidations of Olefins to Enones;Synthesis;2013-07-17

2. Homogeneous CrVI-Catalyzed Benzylic, Allylic and Propargylic Oxidations by tert- Butyl Hydroperoxide;Mini-Reviews in Organic Chemistry;2009-02-01

3. The synthesis and evaluation of 10- and 12-membered ring benzofused enediyne amino acids;Bioorganic & Medicinal Chemistry;2005-11

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