Diprotection of primary amines as N-substituted-2,5-bis[(triisopropylsilyl)oxy]pyrroles (BIPSOP)
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Protective Groups in Organic Synthesis;Greene,1991
2. Protecting Groups;Kocienski,1994
3. Protection of primary amines as N-substituted 2,5-dimethylpyrroles
4. Silicon in synthesis: stabase adducts - a new primary amine protecting group: alkylation of ethyl glycinate
5. Protection of substituted anilines with 1,1,4,4-tetramethyl-1,4-bis(n,n-dimetrylamino)disilethylene
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1. Natural Products and Their Mimics as Targets of Opportunity for Discovery;The Journal of Organic Chemistry;2017-09-15
2. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. An Efficient Method for the Protection of Aromatic Amines with Benzostabase and Its Utility in Anionic Aromatic Transformations;Synlett;2013-10-07
4. Rapid Nickel-Catalyzed Suzuki−Miyaura Cross-Couplings of Aryl Carbamates and Sulfamates Utilizing Microwave Heating;The Journal of Organic Chemistry;2011-01-20
5. ChemInform Abstract: Diprotection of Primary Amines as N-Substituted-2,5-Bis(( triisopropylsilyl)oxy)pyrroles (BIPSOP).;ChemInform;2010-08-03
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