77516-58-6Relevant articles and documents
Assignment of the absolute configuration of blasticidin A and revision of that of aflastatin A
Sakuda, Shohei,Matsumori, Nobuaki,Furihata, Kazuo,Nagasawa, Hiromichi
, p. 2527 - 2531 (2008/02/02)
The absolute configuration of blasticidin A, a strong inhibitor of aflatoxin production by Aspergillus parasiticus, was assigned by adding the data of relative configurations at its diol and pentaol moieties to previously known stereochemistry. Similarity
TOTAL SYNTHESIS OF HALICHONDRINS: HIGHLY STEREOSELECTIVE CONSTRUCTION OF A HOMOCHIRAL PENTASUBSTITUTED H-RING PYRAN INTERMEDIATE FROM α-D-GLUCOSE
Kim, Seokchan,Salomon, Robert G.
, p. 6279 - 6282 (2007/10/02)
The functionality of α-D-Glucose is stereoselectively manipulated exploiting pyranose furanose pyranose interconversions and lactonization for selective masking to achieve a stereocontrolled synthesis of the densely substituted H-ring pyran of halichondrins.
Synthetic studies of rifamycins. II. Syntheses of methyl 2,4,6,7-tetra-deoxy-4-c-methyl-3-O-methyl-α-L-arabino-heptopyranoside-6-ulose and its derivatives utilizable in the construction of the rifamycin ansa chain portion
Nakata,Ikeyama,Takao,Kinoshita
, p. 3252 - 3258 (2007/10/02)
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