Issue 5, 2000

A new cycloheptenone annulation method: use of the bifunctional reagent (Z )-5-iodo-1-tributylstannylpent-1-ene in organic synthesis

Abstract

A new seven-membered annulation method that employs (Z )-5-iodo-1-tributylstannylpent-1-ene (1) as a key reagent and that is exemplified by the conversion of compounds 6, 12, 13, 20, 25, and 26 into the annulation products 11, 18, 19, 24, 33, and 34, respectively, is reported.

Article information

Article type
Paper
Submitted
21 Dec 1999
Accepted
01 Feb 2000
First published
17 Feb 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 635-637

A new cycloheptenone annulation method: use of the bifunctional reagent (Z )-5-iodo-1-tributylstannylpent-1-ene in organic synthesis

E. Piers, S. D. Walker and R. Armbrust, J. Chem. Soc., Perkin Trans. 1, 2000, 635 DOI: 10.1039/A909922K

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