64316-89-8Relevant academic research and scientific papers
Stereochemistry of enacyloxins. Part 5: Synthesis of a C9′-C15′ fragment of enacyloxins, a series of antibiotics from Frateuria sp. W-315
Furukawa, Hiroyuki,Hoshikawa, Hiroaki,Igarashi, Wataru,Yaosaka, Manabu,Yamada, Teiko,Kuwahara, Shigefumi,Kiyota, Hiromasa
, p. 3 - 5 (2011/10/08)
The C9′-C15′ fragment of enacyloxins, a series of antibiotics isolated from Frateuria sp. W-315, was synthesized from diethyl D-tartrate. Copyright by Walter de Gruyter Berlin Boston.
Enantioselective transesterification of 2-methyl-1,3-propanediol derivatives catalyzed by Pseudomonas fluorescens lipase in an organic solvent
Grisenti,Ferraboschi,Manzocchi,Santaniello
, p. 3827 - 3834 (2007/10/02)
The irreversible transesterification of racemic 2-methyl-1,3-propanediol derivatives, the monoethers 3a, 3b, 5a, and the monobenzoate 5b, with vinyl acetate catalyzed by Pseudomonas fluorescens lipase in chloroform affords enantiomerically pure chiral synthons.
ENANTIOSELECTIVE SYNTHESIS OF C3-C10 FRAGMENT (NORTHEASTERN ZONE) OF MAYTANSINOIDS WITH 4-CHIRAL CENTERS (4S,5S,6R,7S)
Meyers, A. I.,Hudspeth, James P.
, p. 3925 - 3928 (2007/10/02)
The major precursor to the maytansinoids containing 4 non-racemic chiral centers has been prepared in gram quantities, suitable for further synthesis.The route to (+)-1 was accomplished in 13 steps including several highly stereocontrolled reactions which
