Mild, orthogonal solid-phase peptide synthesis: use of Nα-dithiasuccinoyl (Dts) amino acids and N-(iso-propyldithio)carbonylproline, together with p-alkoxybenzyl ester anchoring linkages*-Reference-Cited by-同舟云学术

Mild, orthogonal solid-phase peptide synthesis: use of Nα-dithiasuccinoyl (Dts) amino acids and N-(iso-propyldithio)carbonylproline, together with p-alkoxybenzyl ester anchoring linkages*

Published:2009-01-12 Issue:2 Volume:30 Page:177-205
ISSN:0367-8377
Container-title:International Journal of Peptide and Protein Research
language:en
Short-container-title:

Author:

ALBERICIO FERNANDO,BARANY GEORGE

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1987.tb03327.x/fullpdf

Reference77 articles.

1. A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) function

2. Albericio , F. Slomczynska , U. Barany , G. 1984 ORG 152. American Chemical Society, 187th Annual Meeting, St. Louis, Missouri

3. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Reflections on a Copenhagen–Minneapolis Axis in Bioorganic Chemistry;Molecules;2024-03-15

2. Synthetic approaches and structural diversity of triazolylbutanols derived from voriconazole in the antifungal drug development;European Journal of Medicinal Chemistry;2022-03

3. Facile access to polymer supported zinc–salen complex: highly efficient heterogeneous catalyst for synthesizing hydantoins, thiohydantoins and Schiff bases in aqueous medium;Research on Chemical Intermediates;2017-12-14

4. Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach–Weiss–Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones;The Journal of Organic Chemistry;2015-11-09

5. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11