176967-12-7Relevant articles and documents
Synthesis of 3-amino-4-indolyl-2-piperidones: Tryptophan-derived pseudodipeptides
Rodríguez, Ricardo,Diez, Anna,Rubiralta, Mario,Giralt, Ernest
, p. 513 - 517 (2007/10/03)
(αR,3R*,4R*)-N-(2-Acetoxy-1-phenylethyl)-3- allyloxycarbonylamino-4-(1-benzyl-3-indolyl)-2-piperidone (1), a pseudodipeptide which contains a conformationally restricted analogue of tryptophan has been synthesized from anhydride (2) and (R)-(-)-phenylglycinol (3).
Conformationally restricted analogues of tryptophan: Synthesis of chiral 3-amino-4-indolyl-2-piperidones
Rodriguez, Ricardo,Vinets, Imma,Diez, Anna,Rubiralta, Mario,Giralt, Ernest
, p. 3029 - 3059 (2007/10/03)
The {Trp-phenylglycinol} pseudodipeptide (αR,3R*,4R*)-N-(2-acetoxy-1-phenylethyl)-3-amino-4-indolyl-2-piperi done 33 has been synthesized by condensation of the 3-amino-substituted anhydride 30 with (R)-(-)-phenylglycinol followed by reduction of the resulting imide.