Methods to Circumvent a Difficult Coupling in the Solid-Phase Synthesis of Cyclosporine Analogues
Author:
Affiliation:
1. Department of Chemistry and School of Pharmacy, University of Wisconsin, 425 North Charter Street, Madison, Wisconsin 53706-1515
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo980889q
Reference25 articles.
1. Synthesis of cyclosporine. Total syntheses of ?cyclosporin A? and ?cyclosporin H?, two fungal metabolites isolated from the speciesTolypocladium inflatum GAMS
2. Synthesis of D-lysine8-cyclosporine A. Further characterization of BOP-Cl in the 2-7 hexapeptide fragment synthesis
3. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide
4. Solid Phase Synthesis
5. Solid-Phase Synthesis of Cyclosporin Peptides
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3. Solid-Phase Total Synthesis of the Proposed Structure of Coibamide A and Its Derivative: Highly Methylated Cyclic Depsipeptides;European Journal of Organic Chemistry;2015-10-01
4. Solid-Phase Synthesis of Triostin A Using a Symmetrical Bis(diphenylmethyl) Linker System;The Journal of Organic Chemistry;2015-07-14
5. Development of a Practical Process for the Opening of Macrocyclic Cyclosporin A and Amino Acid Deletion;Organic Process Research & Development;2014-11-14
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