A CONVENIENT SYNTHESIS OF THE L-LIKE ENANTIOMER OF 4 %26apos;-METHYL-3-DEAZAARISTEROMYCIN

作者：Chen Chun; Ye Wei; Schneller Stewart W^*

来源：Heterocycles, 2012, 86(1): 697-704.

DOI：10.3987/COM-12-S(N)20

• Carbocyclic Nucleoside
• 6-Chloro-3-deazapurine
• Oxidative Rearrangement

As an entry into L-like 3-deazaaristeromycins, synthesis of the enantiomer of D-like 4%26apos;-methyl-3-deazaaristeromycin is described in 11 steps from a readily accessible cyclopentenone that, in turn, is prepared from D-ribose.

• 出版日期2012-12-31