Conformationally restricted analogues of tryptophan: Synthesis of chiral 3-amino-4-indolyl-2-piperidones

Article abstract of DOI:10.1080/00397919608004608

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.

Full text of DOI:10.1080/00397919608004608

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Synthetic Communications: An
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Conformationally Restricted
Analogues of Tryptophan:
Synthesis of Chiral 3-Amino-4-
indolyl-2-piperidones
Ricardo Rodríguez a , Imma Viñets a , Anna Diez a
Mario Rubiralta a & Ernest Giralt b
,
a Laboratori de Química Orgànica, Facultat de
Farmàcia , Universitat de Barcelona , 08028,
Barcelona, Spain
b Departament de Química Orgànica, Facultat de
Químiques , Universitat de Barcelona , 08028,
Barcelona, Spain
Published online: 21 Aug 2006.
To cite this article: Ricardo Rodríguez , Imma Viñets , Anna Diez , Mario Rubiralta
& Ernest Giralt (1996) Conformationally Restricted Analogues of Tryptophan:
Synthesis of Chiral 3-Amino-4-indolyl-2-piperidones, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:16,
3029-3059, DOI: 10.1080/00397919608004608
To link to this article: http://dx.doi.org/10.1080/00397919608004608
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