Stereocontrolled synthesis of all stereoisomers of the proposed flavolipin

被引:5
作者
Shiozaki, M [1 ]
Deguchi, N [1 ]
Mochizuki, T [1 ]
Nishijima, M [1 ]
机构
[1] NATL INST HLTH & NUTR,DEPT BIOCHEM & CELL BIOL,SHINJUKU KU,TOKYO 162,JAPAN
关键词
D O I
10.1016/0040-4039(96)00705-8
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
All four stereoisomers of flavolipin were synthesized from D-glucose in a stereocontrolled manner. None of them was identical with the reported natural product. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:3875 / 3876
页数:2
相关论文
共 4 条
[1]   VARIOUS KINDS OF LIPOAMINO ACIDS INCLUDING A NOVEL SERINE-CONTAINING LIPID IN AN OPPORTUNISTIC PATHOGEN FLAVOBACTERIUM - THEIR STRUCTURES AND BIOLOGICAL-ACTIVITIES ON ERYTHROCYTES [J].
KAWAI, Y ;
YANO, I ;
KANEDA, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (1-2) :73-80
[2]   MACROPHAGE ACTIVATION BY AN ORNITHINE-CONTAINING LIPID OR A SERINE-CONTAINING LIPID [J].
KAWAI, Y ;
AKAGAWA, K .
INFECTION AND IMMUNITY, 1989, 57 (07) :2086-2091
[3]   SYNTHESIS OF 3'-DEOXYNUCLEOSIDES .2. SYNTHESIS OF 9-(3-DEOXYALDOFURANOSYL) ADENINES DERIVED FROM 3-DEOXY-D-GLUCOSE [J].
MURRAY, DH ;
PROKOP, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1965, 54 (10) :1468-&
[4]   STUDIES ON WB-3559-A, WB-3559-B, WB-3559-C AND WB-3559-D, NEW POTENT FIBRINOLYTIC AGENTS .2. STRUCTURE ELUCIDATION AND SYNTHESIS [J].
UCHIDA, I ;
YOSHIDA, K ;
KAWAI, Y ;
TAKASE, S ;
ITOH, Y ;
TANAKA, H ;
KOHSAKA, M ;
IMANAKA, H .
JOURNAL OF ANTIBIOTICS, 1985, 38 (11) :1476-1486