Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2002(2): 0207-0212
DOI: 10.1055/s-2002-19806
DOI: 10.1055/s-2002-19806
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of a C-9 to C-18 Building Block of the Phenalamides
Further Information
Publication History
Received
29 August 2001
Publication Date:
03 August 2004 (online)


Abstract
In the context of a synthesis of phenalamide A2, the C-9 to C-18 building block 6 was synthesized. The stereogenic centers were generated by alkylation of an Evans oxazolidinone 12 and by a crotylboration reaction using the enantiomerically pure (E)-α-chlorocrotylboronate (4).
Key words
allylboration reaction - diastereoselectivity - natural products - stereoselective synthesis