The synthesis and conformational analysis of a pair of diastereomeric, conformationally constrained peptides with oppposite amide bond geometries

DOI: 10.1016/S0040-4020(01)91222-0

Source and publish data:

Tetrahedron p. 9049 - 9066 (1993)

Update date:2022-07-30

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Authors:

Cumberbatch

North North

Zagotto Zagotto

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Article abstract of DOI:10.1016/S0040-4020(01)91222-0

Eight membered ring containing, conformationally constrained peptides derived from cyclo-[(R)-cysteinyl-(R)-penicillamine] contain a cis amide bond, whilst the diastereomeric peptides derived from cyclo-[(R)-cysteinyl-(S)-penicillamine] contain a transami

Full text of DOI:10.1016/S0040-4020(01)91222-0

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Product name:methyl N-(N-Boc-S-trityl-(R)-cysteinyl)-(R)-penicillamine

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