365542-01-4Relevant articles and documents
The convergent synthesis of novel cytotoxic certonardosterol D2 from diosgenin
Jiang, Biao,Shi, He-ping,Tian, Wei-sheng,Zhou, Wei-shan
, p. 469 - 476 (2008)
Certonardosterol D2, a polyhydroxysterol isolated from starfish Certonardoa semiregularis with exceptionally potent antitumor activity, was stereoselectively synthesized from natural rich diosgenin via the protocol of Julia olefination and Evan
HYDROXAMATE SULFONAMIDES AS CD23 SHEDDING INHIBITORS
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Page 25-26, (2010/02/10)
A class of piperidine and related heterocyclic derivatives, C-substituted by a substituted aryl or heteroaryl moiety, and N-substituted by an ethylsulfonyl group which in turn is substituted at the 2-position by a hydroxamic acid moiety and also by a range of alternative substituents, being potent inhibitors of CD23 shedding, are useful in the treatment and/or prevention of allergic, inflammatory and neoplastic diseases.
An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloproteinase inhibitors
Watson, Robert J.,Batty,Baxter,Hannah,Owen,Montana
, p. 683 - 685 (2007/10/03)
A high yielding and enantioselective synthesis of α-substituted hydroxamic acids as inhibitors of matrix metalloproteinases is described.