New total synthesis of (±)-chuangxinmycin
K Kato, M Ono, H Akita
Index: Kato, Keisuke; Ono, Machiko; Akita, Hiroyuki Tetrahedron Letters, 1997 , vol. 38, # 10 p. 1805 - 1808
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Citation Number: 28
Abstract
(±)-4′-Iodoindolmycenate 6 was stereoselectively converted into the (±)-(2, 3)-syn-2- thioacetoxy ester 16 with retention of C2-stereochemistry in (±)-6. Palladium-catalysed cyclisation of indolyl iodide and the internal C2 thiol group of the substrate (±)-17 derived from (±)-16 gave the (±)-cis methyl ester 2 of natural chuangxinmycin (1).
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