Total Synthesis of Pentabromo??and Pentachloropseudilin, and Synthetic Analogues—Allosteric Inhibitors of Myosin ATPase

…, S Richter, R Fedorov, DJ Manstein…

Index: Martin, Rene; Jaeger, Anne; Bohl, Markus; Richter, Sabine; Fedorov, Roman; Manstein, Dietmar J.; Gutzeit, Herwig O.; Knolker, Hans-Joachim Angewandte Chemie - International Edition, 2009 , vol. 48, # 43 p. 8042 - 8046

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Citation Number: 43

Abstract

The pyrrole ring is a pivotal structural unit of many pharmacologically active natural products, for example, the lamellarins [1] and prodigiosins.[2] Recently, we have developed a novel silver (I)-promoted oxidative cyclization of homopropargylamines to generate pyrroles,[3] which has been applied to the synthesis of the anti-leishmania active (Æ)- harmicine and the antitumor active (Æ)-crispine A.[4] Homopropargylamines are most ...