Enantiomerically Pure α-Amino Acid Synthesis via Hydroboration−Suzuki Cross-Coupling
✍ Scribed by Collier, Philip N.; Campbell, Andrew D.; Patel, Ian; Raynham, Tony M.; Taylor, Richard J. K.
- Book ID
- 111652001
- Publisher
- American Chemical Society
- Year
- 2002
- Tongue
- English
- Weight
- 196 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
The Garner aldehyde-derived methylene alkene has been hydroborated using 9-BBN and the resulting organoborane employed in palladiurn-catalysed Suzuki coupling reactions to produce, offer hydrolysis-oxidation, a range of novel amino acids as their N-BOC protected derivatives.
Protected allylglycine has been hydroborated and the intermediate organoborane employed in Suzuki coupling reactions with a number of ole®nic, aromatic and heteroaromatic bromides and iodides to produce a range of novel a-amino acids in good, unoptimised yields.