Cinchonine-catalyzed in situ generation of unstable and gaseous trifluoroacetaldehyde from its hemiacetal and direct aldol reaction with 2-methoxy-1-phenylethanone-Reference-Cited by-同舟云学术

Cinchonine-catalyzed in situ generation of unstable and gaseous trifluoroacetaldehyde from its hemiacetal and direct aldol reaction with 2-methoxy-1-phenylethanone

Published:2017-06 Issue: Volume:198 Page:76-81
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Funabiki Kazumasa,Yano Yosuke,Hayakawa Ayaka,Inuzuka Toshiyasu,Kubota Yasuhiro,Matsui Masaki

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference30 articles.

1. Enantioselective Alcohol C–H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis

2. Organocatalytic synthesis of carbohydrates

3. For a recent book, see: Modern Aldol Reactions, R. Mahrwald, Ed. (2004).

4. Recent applications of organocatalysts in asymmetric aldol reactions

5. Enantioselective organocatalytic aldol reaction using small organic molecules

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2. Chiral bisoxazoline catalyzed decarboxylative aldol reactions between β-carbonyl acids and trifluoroacetaldehyde hemiacetals as well as trifluoroacetaldehyde: the mechanism, the origin of enantioselectivity and the role of a catalyst;Organic Chemistry Frontiers;2018