Amino acid bromides: their utilization for difficult couplings in solid-phase peptide synthesis-Reference-Cited by-同舟云学术

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Amino acid bromides: their utilization for difficult couplings in solid-phase peptide synthesis

Published:2005-09 Issue:37 Volume:46 Page:6369-6371
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ni Minghong,Esposito Emiliano,Kaptein Bernard,Broxterman Quirinus B.,Dal Pozzo Alma

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. N-Protected amino acid bromides: efficient reagents for the incorporation into peptides of extremely hindered α,α-dialkyl- and α-fluoroalkyl-amino acids

2. Synthesis of acyl halides under very mild conditions

3. Amino Acid Bromides: Their N-Protection and Use in the Synthesis of Peptides with Extremely Difficult Sequences

4. A fast procedure for the reduction of azides and nitro compounds based on the reducing ability of Sn(SR)3-species

Cited by 5 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. Amino acid chlorides: a journey from instability and racemization toward broader utility in organic synthesis including peptides and their mimetics;Tetrahedron;2015-05

2. Postsynthetic Modification of Peptides via Chemoselective N-Alkylation of Their Side Chains;Organic Letters;2012-03-12

3. Protection Reactions;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-04-07

4. You Are Sitting on a Gold Mine!;Synlett;2006-06

5. Combinatorial Chemistry Online Volume 7, Issue 10, October 2005;Combinatorial Chemistry - an Online Journal;2005-10

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