## 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 βFull Textβ option. The original article is trackable v
ChemInform Abstract: Stereoselective Routes to E and Z Straight-Chain Primary Allylic Amines.
β Scribed by B. TOMASSY; A. ZWIERZAK
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
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 by reduction of (I) with LiAlH 4 using a known protocol. -(TOMASSY, B.;
π SIMILAR VOLUMES
## 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 βFull Textβ option. The original article is trackable v
The title method is based on the recently discovered radical fragmentation of 2-fluoro-6-pyridinoxy derivatives of vinylsulfones. The radical addition of xanthates to these alkenes leads to the formation of (E)-vinylsulfone adducts, which are desulfonylated by treatment with sodium dithionite and so