SYNTHESIS AND ABSOLUTE-CONFIGURATION OF TREHAZOLIN AMINOCYCLITOL MOIETY
被引:18
作者:
KOBAYASHI, Y
论文数: 0引用数: 0
h-index: 0
机构:
SANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPANSANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPAN
KOBAYASHI, Y
[1
]
MIYAZAKI, H
论文数: 0引用数: 0
h-index: 0
机构:
SANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPANSANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPAN
MIYAZAKI, H
[1
]
SHIOZAKI, M
论文数: 0引用数: 0
h-index: 0
机构:
SANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPANSANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPAN
SHIOZAKI, M
[1
]
机构:
[1] SANKYO CO LTD,NEW LEAD RES LABS,HIROMACHI 1-2-58,SHINAGAWA KU,TOKYO 140,JAPAN
Optically active [1R-(1alpha,2beta,3alpha,4beta,5beta)]-5-acetamide-1-acetoxymethyl-1,2,3,4-tetraacetoxycyclopentane 2 was synthesized from D-glucose. Compound 2 was identical in all respects with the hexaacetate derived from the natural trehazolin aminocyclitol moiety.