Loss of the tert-butyloxycarbonyl (Boc) protecting group under basic conditions-Reference-Cited by-同舟云学术

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Loss of the tert-butyloxycarbonyl (Boc) protecting group under basic conditions

Published:1994-07 Issue:30 Volume:35 Page:5409-5412
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Curran Timothy P.,Pollastri Michael P.,Abelleira Susan M.,Messier Renee J.,McCollum Theresa A.,Rowe Campbell G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. New Amine-masking Groups for Peptide Synthesis

2. t-Butyloxycarbonylamino Acids and Their Use in Peptide Synthesis

3. Oxidative Reactions of Hydrazines. IV. Elimination of Nitrogen from 1,1-Disubstituted-2-arenesulfonhydrazides1-4

4. Amine Protecting Groups;Geiger,1981

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1. “All-Aqueous” Tandem Boc-Deprotection and Alkylation of N-Bocbenzimidazole Derivatives under Visible Light with Alkyl Aryl Diazoacetates: Application to Site-Selective Insertion of Carbenes into the N–H Bond of Purines;The Journal of Organic Chemistry;2022-12-29

2. Mild deprotection of the N-tert-butyloxycarbonyl (N-Boc) group using oxalyl chloride;RSC Advances;2020

3. Strategy for O-Alkylation of Serine and Threonine from Serinyl and Threoninyl Acetic Acids by Photoinduced Decarboxylative Radical Reactions: Connection between Serine/Threonine and Carbohydrates/Amino Acids at the Side Chain;The Journal of Organic Chemistry;2018-03-09

4. Studies on cyclization reactions of 3-amino-2,4-dihydroxybutanoic acid derivatives;Organic & Biomolecular Chemistry;2017

5. An efficient synthesis of 1′,4′-dihydro-2′H-spiro[azetidin-2,3′-quinolin]-2′-one;Research on Chemical Intermediates;2016-06-20

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