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Showing 1-11 of 11 results for "272728" within Papers
Journal of the Chemical Society. Perkin Transactions 1, 1681-1681 (1985)
Xing Tan et al.
Journal of the American Chemical Society, 134(39), 16163-16166 (2012-09-20)
The cascade oxidative annulation reactions of benzoylacetonitrile with internal alkynes proceed efficiently in the presence of a rhodium catalyst and a copper oxidant to give substituted naphtho[1,8-bc]pyrans by sequential cleavage of C(sp(2))-H/C(sp(3))-H and C(sp(2))-H/O-H bonds. These cascade reactions are highly
Heterocycles, 20, 2393-2393 (1983)
Journal of the Chemical Society. Perkin Transactions 1, 2581-2581 (1985)
L P Davies et al.
Life sciences, 34(22), 2117-2128 (1984-05-28)
A large number of nitrogen heterocycles structurally related to caffeine and theophylline have been tested for activity as adenosine antagonists. Preliminary screening, utilizing displacement of [3H]N6-phenylisopropyladenosine (PIA) binding to rat brain membranes, identified several pyrazolo[3,4-d]pyrimidines with potential antagonist activity. These
Journal of Heterocyclic Chemistry, 15, 57-57 (1978)
Heterocycles, 14, 639-639 (1980)
Synthesis, 513-513 (1982)
Organic preparations and procedures international, 18, 85-85 (1986)
Heterocycles, 23, 2013-2013 (1985)
Hwi Young Yun et al.
Drug design, development and therapy, 9, 4259-4268 (2015-09-09)
Tyrosinase is the most prominent target for inhibitors of hyperpigmentation because it plays a critical role in melaninogenesis. Although many tyrosinase inhibitors have been identified, from both natural and synthetic sources, there remains a considerable demand for novel tyrosinase inhibitors
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