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Aldecalmycin, a new antimicrobial antibiotic from Streptomyces. III. Determination of absolute configuration
R Sawa1, Y Takahashi, H Nakamura
1Institute of Microbial Chemistry, Tokyo, Japan.
The Journal of Antibiotics
|November 1, 1994
Abstract:
The planar structure of aldecalmycin (1) had been determined in the previous paper, together with the conformations of the substituted trans decalin ring having one double bond and the sugar: beta-glucopyranoside type. The absolute configuration of 1 was a following problem to be solved. X-Ray crystallographic analysis of crystalline 4'-6'-O-benzylidenedihydroaldecalmycin (4) revealed the relative configuration. On the other hand, the stereoisomerism of the sugar was determined to be D by the optical rotation value of tetra-O-acetyl-alpha-methylglucopyranoside derived from 1. These results established the absolute configuration of 1.