Approaching sub-ppm-level asymmetric organocatalysis of a highly challenging and scalable carbon–carbon bond forming reaction-Reference-Cited by-同舟云学术

Approaching sub-ppm-level asymmetric organocatalysis of a highly challenging and scalable carbon–carbon bond forming reaction

Published:2018-07-09 Issue:8 Volume:10 Page:888-894
ISSN:1755-4330
Container-title:Nature Chemistry
language:en
Short-container-title:Nature Chem

Author:

Bae Han Yong^ORCID,Höfler Denis,Kaib Philip S. J.,Kasaplar Pinar,De Chandra Kanta,Döhring Arno,Lee Sunggi,Kaupmees Karl,Leito Ivo^ORCID,List Benjamin^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Chemical Engineering,General Chemistry

Link

http://www.nature.com/articles/s41557-018-0065-0.pdf

Reference37 articles.

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3. Mahrwald, R. Diastereoselection in Lewis-acid-mediated aldol additions. Chem. Rev. 99, 1095–1120 (1999).

4. Machajewski, T. D. & Wong, C.-H. The catalytic asymmetric aldol reaction. Angew. Chem. Int. Ed. 39, 1352–1375 (2000).

5. Mahrwald, R. Modern Aldol Reactions (Wiley-VCH, Weinheim, 2004).

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