Issue 14, 1995

A short and efficient route to (±)-anatoxin-a

Abstract

A new route to Anatoxin-a1 is reported which involves a tandem methyllithium mediated ring opening/intramolecular cyclisation as a key step to provide the required 2-acetyl-9-azabicyclo [4.2.1] nonane ring structure in one synthetic operation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1461-1462

A short and efficient route to (±)-anatoxin-a

P. J. Parsons, N. P. Camp, J. M. Underwood and D. M. Harvey, J. Chem. Soc., Chem. Commun., 1995, 1461 DOI: 10.1039/C39950001461

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