Highly Diastereoselective Preparation of Aldol Products Using New Functionalized Allylic Aluminum Reagents-Reference-Cited by-同舟云学术

Highly Diastereoselective Preparation of Aldol Products Using New Functionalized Allylic Aluminum Reagents

Published:2014-01-30 Issue:3 Volume:16 Page:956-959
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shen Zhi-Liang¹,Peng Zhihua¹,Yang Chun-Ming¹,Helberg Julian¹,Mayer Peter¹,Marek Ilan²,Knochel Paul¹

Affiliation:

1. Department Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377 München, Germany

2. The Mallat Family Laboratory of Organic Chemistry, Schulich Faculty of Chemistry and Lise Meitner-Minerva Center for Computational Quantum Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000, Israel

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403692k

Reference70 articles.

1. Modern Aldol Reactions

2. Proline-Catalyzed Direct Asymmetric Aldol Reactions

3. Catalytic Asymmetric Synthesis of anti-1,2-Diols

4. Synthesis ofβ-Hydroxyaldehydes with Stereogenic Quaternary Carbon Centers by Direct Organocatalytic Asymmetric Aldol Reactions

5. Highly Diastereo- and Enantioselective Direct Aldol Reactions in Water

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