204275-88-7Relevant academic research and scientific papers
Toward a total synthesis of an aglycone of spiramycin; installation of the hydroxy groups at C-4 and C-5: A model study
Oddon,Uguen,De Cian,Fischer
, p. 1149 - 1152 (1998)
The stereochemical course of the osmium-mediated bis-hydroxylation of the allylic derivative 6c, whose the structure is closely related to that of a C-1/C-7 fragment of the title aglycone, has been established unambiguously by X-ray analysis of a carboxylic[ic acid derived from one of the two diastereomeric diols which formed.
