A Simple Stereoselective Access to α-Trifluoromethylated Piperidines.
✍ Scribed by Annabelle Bariau; Jean-Philippe Roblin; Yves Troin; Jean-Louis Canet
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 25 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## 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
## Pyridine derivatives R 0380 A One-Pot Synthesis of Doubly Unsaturated Trifluoromethyl Amines: Easy Access to CF3-Substituted Piperidines. -Starting from acetaldimines (I), double allylation can be performed in one pot by use of activated zinc. In some cases, the addition of stoichiometric or ca