887769-08-6Relevant articles and documents
Asymmetric synthesis of the polyol subunit of the macrolide antibiotic, ossamycin
Kutsumura, Noriki,Nishiyama, Shigeru
, p. 5707 - 5709 (2005)
An asymmetric synthesis of the C1-C16 polyol subunit of the macrolide antibiotic, ossamycin, has been achieved through stepwise carbon-chain elongation reaction from D-glucose.
Asymmetric synthesis of the polyol subunit of the macrolide antibiotic, ossamycin: A unique approach utilizing stereochemical specificity
Kutsumura, Noriki,Nishiyama, Shigeru
, p. 468 - 478 (2007/10/03)
An asymmetric synthesis of the C1-C16 polyol subunit 2 of the macrolide antibiotic ossamycin (1) has been achieved through stepwise carbon-chain elongation reaction from D-glucose, based on a chiral pool approach. An outstanding point of this strategy is