Control of the Regio- and Diastereoselectivity for the Preparation of Highly Functionalized Terpenic Cyclopentanes through Radical Cyclization-Reference-Cited by-同舟云学术

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Control of the Regio- and Diastereoselectivity for the Preparation of Highly Functionalized Terpenic Cyclopentanes through Radical Cyclization

Published:2011-07-28 Issue:26 Volume:2011 Page:5002-5011
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Arteaga Jesús F.,Diéguez Horacio R.,González-Delgado José A.,Quílez del Moral José F.,Barrero Alejandro F.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201100400/fullpdf

Reference63 articles.

1. Stereocontrolled Preparation of Fully Substituted Cyclopentanes: Relevance to Total Synthesis

2. Substrate-directable chemical reactions

3. Directed Dihydroxylation of Cyclic Allylic Alcohols and Trichloroacetamides Using OsO4/TMEDA

4. The tethered nitrogen in natural products synthesis

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5. Regioselective Cleavage of Electron‐Rich Double Bonds in Dienes to Carbonyl Compounds with [Fe(OTf) 2 (mix‐BPBP)] and a Combination of H 2 O 2 and NaIO 4;European Journal of Inorganic Chemistry;2015-04-27

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