Synthesis and hydrogenation of (E)-γ-aryl-γ-morpholino-α-trifluoromethylated allyl alcohols through the reaction of trifluoroacetaldehyde ethyl hemiacetal with enamines-Reference-Cited by-同舟云学术

Synthesis and hydrogenation of (E)-γ-aryl-γ-morpholino-α-trifluoromethylated allyl alcohols through the reaction of trifluoroacetaldehyde ethyl hemiacetal with enamines

Published:2010-05 Issue:18 Volume:66 Page:3283-3289
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Funabiki Kazumasa,Murase Yoshihiro,Furuno Yudai,Kubota Yasuhiro,Ebihara Masahiro,Matsui Masaki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference90 articles.

1. For the reaction with boron enolates, see:

2. Diastereo-Face Selectivity in the Aldol Reaction of Boryl Enolate Derived from Oppolzer's Sultam.

3. Reversal of stereoselectivity in the Evans aldol reaction of α,α-difluoro and α,α,α-trifluoro carbonyl compounds

4. Reversal of π-face selectivity in the Evans aldol reaction with fluoral: A computational study on the transition states using semiempirical calculations

5. GENERATION AND USE OF LITHIUM PENTAFLUOROPROPEN-2-OLATE: 4-HYDROXY-1,1,1,3,3-PENTAFLUORO-2-HEXANONE HYDRATE

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1. An asymmetric tertiary carbon center with a tetrafluoroethylene (–CF 2 CF 2 –) fragment: Novel construction method and application in a chiral liquid crystalline molecule;Journal of Fluorine Chemistry;2018-03

2. Stereoselective Synthesis of Nitrogen-Containing Compounds from Enamines;The Journal of Organic Chemistry;2017-10-06

3. ChemInform Abstract: Synthesis and Hydrogenation of (E)-γ-Aryl-γ-morpholino-α-trifluoromethylated Allyl Alcohols Through the Reaction of Trifluoroacetaldehyde Ethyl Hemiacetal with Enamines.;ChemInform;2010-08-26