Design and synthesis of a cis-Gly-Pro, type-VI turn, dipeptide mimetic and its use in Fmoc-solid phase peptide synthesis

DOI: 10.1016/S0040-4039(00)75983-1

Source and publish data:

Tetrahedron Letters p. 861 - 864 (1994)

Update date:2022-09-26

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Authors:

Gramberg

Robinson

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Article abstract of DOI:10.1016/S0040-4039(00)75983-1

The Fmoc-protected bicyclic molecules 7 and 8 have been produced as cis-Gly-Pro peptide mimetics in nine synthetic steps starting from optically pure (R)-2-allylproline. Their use in solid-phase peptide synthesis has been demonstrated by their incorporati

Full text of DOI:10.1016/S0040-4039(00)75983-1

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Product name:8a(1H)-Indolizinecarboxylicacid,6-aminohexahydro-5-oxo-,(6R-cis)-(9CI)

Cas No:172039-41-7

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