Journal of Medicinal Chemistry p. 343 - 349 (1991)
Update date:2022-07-29
Topics:
Tseng, Christopher K-H.
Marquez, Victor E.
Milne, George W. A.
Wysocki, Roland J.
Mitsuya, Hiroaki
et al.
Two ring-expanded analogues (compounds 2 and 3) of the anti-HIV fermentation product oxetanocin A (1) were synthesized from commercially available diacetone D-glucose.Antiviral testing against HIV in ATH8 cells revealed that the ring-expanded analogue 2 p
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