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Synthesis 2005(7): 1087-1094
DOI: 10.1055/s-2005-861862
DOI: 10.1055/s-2005-861862
PAPER
© Georg Thieme Verlag Stuttgart · New YorkStereoselective Synthesis of (1R,5S)-4-[(E)-Alkylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-ones
Further Information
Received
3 November 2004
Publication Date:
09 March 2005 (online)
Publication History
Publication Date:
09 March 2005 (online)

Abstract
Various (1R,5S)-4-[(E)-alkylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-ones were prepared, stereoselectively, via coupling of (1R,5S)-4-[(E)-(dimethylamino)methylidene]-1,8,8-trimethyl-2-oxabicyclo[3.2.1]octan-3-one with Grignard reagents, potassium cyanide, and 2-methyl-1H-indole.
Key words
Grignard reactions - chiral pool - coupling - terpenoids - enaminones
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References
Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC 254265-254268. Copies of the data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html.