Journal of Organic Chemistry p. 4029 - 4032 (1982)
Update date:2022-07-29
Topics:
Nitz, Theodore J.
Lindsey, John
Stammer, Charles H.
An attempt to prepare dehydro analogues of 1 gave the expected tripeptide 2a, but rearrangement of a thiazolone derivative of ΔZ-Phe made only a thiazolinecarboxylic acid (8) available.The latter was also converted into a tripeptide (11) and both compounds, 2a and 11, showed moderate angiotensin converting enzyme inhibition.
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Doi:10.1016/j.ejmech.2011.08.024
(2011)Doi:10.1246/bcsj.55.1599
(1982)Doi:10.1021/ja00386a029
(1982)Doi:10.1021/jm00353a006
(1982)Doi:10.1248/cpb.30.2410
(1982)Doi:10.1246/cl.1982.1151
(1982)
