88671-02-7Relevant articles and documents
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.
A mild and versatile method for the tetrahydropyranylation of alcohols and their detetrahydropyranylation
Yadav,Srinivas, Dale,Reddy, Gondi Sudershan
, p. 1399 - 1404 (2007/10/03)
An efficient and mild method for tetrahydropyranylation of alcohols and their detetrahydropranylation using NH4Cl is described. This protocol provides a useful alternative tetrahydropyranylation of alcohols and their deprotection at different pH.
The synthesis of the C-9 to C-21 sector of discodermolide: An efficient route to the C13-14 Z-trisubstituted alkene
Yang, Ge,Myles, David C.
, p. 2503 - 2504 (2007/10/02)
The synthesis of the C-9 to C-21 sector of the immunosuppressive marine natural product discodermolide is described. The C-9 to C-15 subunit is synthesized in five steps from aldehyde 5 using the diene aldehyde cyclocondensation reaction. Diastereoselective alkylation of the previously synthesized C-16 to C-21 subunit by a suitably functionalized C-9 to C-15 synthon (3) leads to the C-9 to C-21 sector of discodermolide.
