Absolute stereochemistry of penaresidins A and B

被引：39

作者：

Kobayashi, J ^{[1
]}

Tsuda, M ^{[1
]}

Cheng, JF ^{[1
]}

Ishibashi, M ^{[1
]}

Takikawa, H ^{[1
]}

Mori, K ^{[1
]}

机构：

[1] SCI UNIV TOKYO,FAC SCI,DEPT CHEM,TOKYO 162,JAPAN

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 37期

关键词：

D O I：

10.1016/S0040-4039(96)01465-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Absolute stereochemistry at C-15 in penaresidins A (1) and B (2) was established to be S on the basis of H-1 NMR data of the tri-O-MTPA esters, indicating that the absolute configurations of 1 and 2 are 2S, 3R, 4S, 15S (1 and 2), and 16S (1). Copyright (C) 1996 Elsevier Science Ltd

引用

页码：6775 / 6776

页数：2

共 6 条

[1] PENARESIDIN-A AND PENARESIDIN-B, 2 NOVEL AZETIDINE ALKALOIDS WITH POTENT ACTOMYOSIN ATPASE-ACTIVATING ACTIVITY FROM THE OKINAWAN MARINE SPONGE PENARES SP
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[3] HIGH-FIELD FT NMR APPLICATION OF MOSHER METHOD - THE ABSOLUTE-CONFIGURATIONS OF MARINE TERPENOIDS
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (11) : 4092 - 4096
[4] SYNTHESIS OF PENARESIDIN-A, AN AZETIDINE ALKALOID WITH ACTOMYOSIN ATPASE-ACTIVATING PROPERTY
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MAEDA, T
MORI, K
[J]. TETRAHEDRON LETTERS, 1995, 36 (42) : 7689 - 7692
[5] TAKIKAWA H, 1995, 37 S CHEM NAT PROD T, P49
[6] TAKIKAWA H, IN PRES J CHEM SO P1

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