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Synthesis 2007(8): 1154-1158
DOI: 10.1055/s-2007-965993
DOI: 10.1055/s-2007-965993
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of (S,R,R,R)-α,α′-Iminobis(methylene)bis(6-fluoro-3H,4H-dihydro-2H-1-benzopyran-2-methanol)
Further Information
Received
12 October 2006
Publication Date:
23 March 2007 (online)
Publication History
Publication Date:
23 March 2007 (online)
Abstract
The β1-adrenergic antagonist (S,R,R,R)-α,α′-iminobis(methylene)bis(6-fluoro-3H,4H-dihydro-2H-1-benzopyran-2-methanol) was synthesized from natural chiral pool starting materials through an efficient, convergent synthetic strategy. The cyclization mechanism of the key step was investigated using computer modeling and is discussed.
Key words
(S,R,R,R)-nebivolol - chiral pool - cyclization - synthesis design
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