Enantioselective Total Synthesis of the Cyclophilin-Binding Immunosuppressive Agent Sanglifehrin A
- 1 October 2001
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 113 (19) , 3744-3748
- https://doi.org/10.1002/1521-3757(20011001)113:19<3744::aid-ange3744>3.0.co;2-b
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Total Synthesis of the Novel Immunosuppressant Sanglifehrin AJournal of the American Chemical Society, 2000
- Toward a Total Synthesis of the Immunosuppressant Sanglifehrin A. Preparation of Two Relay Compounds by Degradation and Their Use in the Reassembly of the Natural ProductThe Journal of Organic Chemistry, 1999
- Synthesis of the tripeptide (C1–N12) and hydroxylated hexadecene (C26–C41) domains of sanglifehrin A and CTetrahedron Letters, 1999
- Total Synthesis of Sanglifehrin AAngewandte Chemie International Edition in English, 1999
- Totalsynthese von Sanglifehrin AAngewandte Chemie, 1999
- A synthesis of the C1N12 tripeptide fragment of sanglifehrin ATetrahedron Letters, 1999
- Rapamycin and FK506 binding proteins (immunophilins)Journal of the American Chemical Society, 1991
- Inhibition of FKBP Rotamase Activity by Immunosuppressant FK506: Twisted Amide SurrogateScience, 1990
- A receptor for the immuno-suppressant FK506 is a cis–trans peptidyl-prolyl isomeraseNature, 1989
- A cytosolic binding protein for the immunosuppressant FK506 has peptidyl-prolyl isomerase activity but is distinct from cyclophilinNature, 1989