Enantioselective Iridium-Catalyzed Vinylogous Reformatsky-Aldol Reaction from the Alcohol Oxidation Level: Linear Regioselectivity by Way of Carbon-Bound Enolates-Reference-Cited by-同舟云学术

Enantioselective Iridium-Catalyzed Vinylogous Reformatsky-Aldol Reaction from the Alcohol Oxidation Level: Linear Regioselectivity by Way of Carbon-Bound Enolates

Published:2011-03-04 Issue:15 Volume:123 Page:3555-3558
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Hassan Abbas,Zbieg Jason R.,Krische Michael J.

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201100646/fullpdf

Reference102 articles.

1. The Principle of Vinylogy.

2. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

3. Recent Advances in Asymmetric Aldol Reaction of Masked Acetoacetic Esters Promoted by Ti(IV) / BINOL: A New Methodology, Non-Linear Effects and Autoinduction

4. Katalytische enantioselektive vinyloge Aldolreaktionen

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