Acyclic stereoselection in α-amidoalkylation reactions
✍ Scribed by Kenn E. Harding; Clark S. Davis
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 296 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
By an appropriate choice of cation, three of the four possible aldols from the reactions of the chiral a-silyloxy ketone 1 with aldehydes may be obtained. The Z lithium enolate provides 6, the Z boron enolate gives 7, and the E magnesium enolate affords 8.
## Abstract Metathesis polymers of norbornene and 1‐methylnorbornene were prepared using a well‐defined aryloxy(chloro)neopentylidene tungsten initiator which behaves in a stereo and regioselective manner giving predominantly __cis__ polymers and a strong head‐to‐tail bias in the case of 1‐methylno