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ChemInform Abstract: Stereoselective Access to Substituted [(E)- or (Z)-1-(Trifluoromethyl)allyl]amines.

✍ Scribed by Guillaume Magueur; Benoit Crousse; Daniele Bonnet-Delpon

Publisher
John Wiley and Sons
Year
2008
Weight
57 KB
Volume
39
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable via the β€œReferences” option.

πŸ“œ SIMILAR VOLUMES

Stereoselective Access to Substituted [(
Stereoselective Access to Substituted [(E)- or (Z)-1-(Trifluoromethyl)allyl]amines
✍ Guillaume Magueur; Benoit Crousse; DaniΓ¨le Bonnet-Delpon πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 200 KB πŸ‘ 1 views

## Abstract Hydrometallation reactions, for example, hydroboration and hydroalumination, on [1‐(trifluoromethyl)propargyl]amines lead stereoselectively to the corresponding [(__Z__)‐ and (__E__)‐1‐(trifluoromethyl)allyl]amines in good yields; (__Z__)‐ and (__E__)‐allylamines with a free amino group

ChemInform Abstract: Stereoselective Rou
ChemInform Abstract: Stereoselective Routes to E and Z Straight-Chain Primary Allylic Amines.
✍ B. TOMASSY; A. ZWIERZAK πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB

Stereoselective Routes to E and Z Straight-Chain Primary Allylic Amines. -An efficient, general and versatile access to straight-chain primary (Z)-allylic amines (IX) from alk-2-yn-1-ols (I) is described involving catalytic reduction of (VIII). The corresponding (E)-allylic amines can be obtained b