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Synlett 2008(3): 313-324
DOI: 10.1055/s-2008-1032060
DOI: 10.1055/s-2008-1032060
ACCOUNT
© Georg Thieme Verlag Stuttgart · New York
New Strategies for the Synthesis of Hexahydropyrroloindole Alkaloids Inspired by Biosynthetic Hypotheses
Further Information
Received
28 October 2007
Publication Date:
16 January 2008 (online)
Publication History
Publication Date:
16 January 2008 (online)
Abstract
This account concerns synthetic studies of dimeric hexahydropyrroloindole alkaloids.
1 Introduction
2 A Biosynthetic Hypothesis for Calycanthaceous Alkaloids
3 Background
3.1 Prior Synthetic Studies of Calycanthaceous Alkaloids
3.2 Overman’s Enantioselective Syntheses of Chimonanthine
4 Our Work on the Syntheses of Hexahydropyrroloindole Alkaloids
4.1 Early Synthetic Studies of Chimonanthine
4.2 Development of a Cobalt(I)-Promoted Reductive Dimerization Strategy
4.3 New Directions and Our Biosynthetic Hypothesis for Dimeric Indole Alkaloids
5 Conclusion
Key words
alkaloids - total synthesis - dimerizations - enantioselectivity - indoles
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