Journal of Medicinal Chemistry p. 2526 - 2535 (1993)
Update date:2022-07-30
Topics:
Mertens, Alfred
Zilch, Harald
Koenig, Bernhard
Schaefer, Wolfgang
Poll, Thomas
et al.
A series of substituted 2,3-dihydrothiazolo<2,3-a>isoindol-5(9bH)-ones and related compounds 1-73 were synthesized and evaluated for their ability to inhibit reverse transcriptase (RT) of the human immune deficiency virus 1 (HIV-1) and replication of HIV-
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Doi:10.1021/om980102m
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