82160-01-8Relevant articles and documents
Aureolic acid antibiotics: Synthesis of the cyclohexenone segment from D-glucose
Gurjar, M.K.,Devi, T. Rama,Reddy, K.L.N.,Sharma, P.A.,Dhar, T.G. Murali
, p. 995 - 1003 (2007/10/02)
The cyclohexenone segment which is common to all the aureolic acid group of antibiotics has been synthesised from D-glucose.Two routes have been designed to obtain methyl 3-O-benzyl-6-deoxy-2-O-methyl-D-galactopyranoside.Route-A involves the introduction
SYNTHESIS OF 2,3-ANHYDRO- AND 3,4-ANHYDRO-HEXOPYRANOSIDES HAVING A METHYL BRANCH ON THE OXIRANE RING, AND THEIR REACTIONS WITH SOME LITHIUM METHYLCUPRATE REAGENTS
Yoshimura, Juji,Kawauchi, Nobuya,Yasumori, Toshio,Sato, Ken-Ichi,Hashimoto, Hironobu
, p. 255 - 274 (2007/10/02)
Three 2,3-anhydroaldohexopyranosides having a 2-C-methyl or 3-C-methyl branch, as well as three 3,4-anhydroaldohexopyranosides having a 3-C-methyl (7) or 4-C-methyl branch, were newly synthesized.The reactions of these, together with those of a known 3-C-