Selective and potent Type-A CCK receptor agonists of formula (I):X--Y--Z--Q (I)or a pharmaceutically acceptable salt thereof, wherein,X is selected from STR1 Y is selected from STR2 Z is STR3 and Q is STR4 or pharmaceutically-acceptable
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(2008/06/13)
Synthesis of α,α-Disubstituted α-Amino Acid Amides by Phase-Transfer Catalyzed Alkylation
α,α-Disubstituted α-amino acid amides were prepared in 17-88 percent chemical yield by the phase-transfer catalyzed alkylation of N-benzylidene α-H amino acid amides, followed by weak acidic hydrolysis of the Schiff bases.
Kaptein, Bernard,Boesten, Wilhelmus H. J.,Broxterman, Quirinus B.,Schoemaker, Hans E.,Kamphuis, Johan
p. 6007 - 6010
(2007/10/02)
Synthesis of α-benzyl γ-lactam, α-benzyl δ-lactam, and α-benzylproline derivatives as confomationally restricted analogues of phenylalaninamide
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Holladay,Nadzan
p. 3900 - 3905
(2007/10/02)
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