Highly Regioselective Lewis Acid-Mediated Aldol Additions at the More Encumbered α-Side of Unsymmetrical Ketones-Reference-Cited by-同舟云学术

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Highly Regioselective Lewis Acid-Mediated Aldol Additions at the More Encumbered α-Side of Unsymmetrical Ketones

Published:1998-01-01 Issue:2 Volume:120 Page:413-414
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Mahrwald Rainer¹,Gündogan Bilgi¹

Affiliation:

1. Institut für Organische und Bioorganische Chemie der Humboldt-Universität Hessische Strasse 1-2, D-10 115 Berlin, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja973453l

Reference25 articles.

Cited by 41 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. Biocatalytic Aldol Addition of Simple Aliphatic Nucleophiles to Hydroxyaldehydes;ACS Catalysis;2018-08-08

2. Formation of Aldehydes and Ketones by Condensation Reactions;Comprehensive Organic Transformations;2018-02-28

3. Phase-vanishing method applied to condensation reactions using TiCl 4;Journal of Fluorine Chemistry;2017-05

4. Nucleophilic Species That Form Carbon-Carbon Bonds;Organic Synthesis;2017

5. Stereoselective TiCl4-Mediated Aldol Reactions Starting from Acylsilanes;European Journal of Organic Chemistry;2014-12-16

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