Templates for intramolecular O,N-acyl transfer via cyclic intermediates derived from mercury derivatives of L-cysteine: progress toward a mercury-based thiol capture strategy
- 1 August 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (16) , 3853-3858
- https://doi.org/10.1021/jo00277a022
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Rational design of templates for intramolecular O,N-acyl transfer via medium-sized cyclic intermediates derived from L-cysteine. Definition of an experimental maximum in effective molarity through the study of "tunable" templatesThe Journal of Organic Chemistry, 1989
- Peptide synthesis by prior thiol capture. 2. Design of templates for intramolecular O,N-acyl transfer. 4,6-Disubstituted dibenzofurans as optimal spacing elementsThe Journal of Organic Chemistry, 1986
- Peptide synthesis by prior thiol capture. 1. A convenient synthesis of 4-hydroxy-6-mercaptodibenzofuran and novel solid-phase synthesis of peptide-derived 4-(acyloxy)-6-mercaptodibenzofuransThe Journal of Organic Chemistry, 1986