Efficient and selective cleavage of the t-butoxycarbonyl group from di-t-butylimidodicarbonate using catalytic bismuth(III) bromide in acetonitrile
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Protective Groups in Organic Synthesis;Greene,1999
2. Protecting Groups;Kocienski,1994
3. Acidity of imidodicarbonates and tosylcarbamates in dimethyl sulfoxide. Correlation with yields in the Mitsunobu reaction
4. Mitsunobu reactions of n-alkyl and n-acyl sulfonamides-an efficient route to protected amines
5. tert-Butyl [[2-(trimethylsilyl)ethyl]sulfonyl]carbamate: a new reagent for use in Mitsunobu reactions
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2. Nascent-HBr-Catalyzed Removal of Orthogonal Protecting Groups in Aqueous Surfactants;The Journal of Organic Chemistry;2019-12-25
3. The crystal structure of tert-butyl (tert-butoxy(oxo)methyl)(5-bromo-2-fluorophenyl)carbamate, C16H21BrFNO4;Zeitschrift für Kristallographie - New Crystal Structures;2019-12-18
4. Efficient and Chemoselective Deprotection of N-t-Butyloxycarbonyl Group Mediated by Selectfluor;Chinese Journal of Organic Chemistry;2018
5. Bismuth Tribromide;Encyclopedia of Reagents for Organic Synthesis;2017-09-04
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