183896-07-3Relevant academic research and scientific papers
Mechanism of amido-thiourea catalyzed enantioselective imine hydrocyanation: Transition state stabilization via multiple non-covalent interactions
Zuend, Stephan J.,Jacobsen, Eric N.
supporting information; experimental part, p. 15358 - 15374 (2010/02/16)
An experimental and computational investigation of amido-thiourea promoted imine hydrocyanation has revealed a new and unexpected mechanism of catalysis. Rather than direct activation of the imine by the thiourea, as had been proposed previously in relate
DERIVATIVES OF SUCCINAMIDE AND THEIR USE AS METALLOPROTEINASE INHIBITORS
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, (2008/06/13)
Compounds of formula (I), wherein X is a--CO 2 H or--CONHOH group; STR1 R 4 is a group--CHR x R y wherein R. sup.x and R. sup.y independently represent optionally substituted phenyl or monocyclic heteroaryl rings, which optionally may be linked covalently
Novel N-substituted alpha aminoacid amides as calcium channel modulators
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, (2008/06/13)
The compounds of formula I and derivatives thereof have been found to be active in tests that show modulation of voltage-dependent calcium channels, and are thus indicated for use in the treatment of diseases in which such modulation is beneficial, in par
