A facile radical induced selective removal of N-propargyl protecting groups using low valent titanium reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Protecting Group Strategies in Organic Synthesis
2. Protective Groups in Organic Synthesis;Green,1991
3. Simultaneous Deprotection and Purification of BOC-amines Based on Ionic Resin Capture
4. Low-Valent Titanium Mediated Deprotection of N-Allyl/Benzyl Amines: A New Approach
5. Low-Valent Titanium Mediated Reductive Deoxygenation of Carbonyls to MethylenesViaCarbon-Nitrogen Bond Cleavage in N-(Arylmethyl) Anilines
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1. Hydrazine-assisted one-pot depropargylation and reduction of functionalized nitro calix[4]arenes;Russian Chemical Bulletin;2023-04
2. Preparation, application and recycling of a catalytic microflow reactor based on polylactic acid;Applied Surface Science;2021-12
3. Selective cleavage of the N-propargyl group from sulfonamides and amides under ruthenium catalysis;Tetrahedron Letters;2018-05
4. Synthetic Reactions Using Low-valent Titanium Reagents Derived from Ti(OR)4or CpTiX3(X = O-i-Pr or Cl) in the Presence of Me3SiCl and Mg;The Chemical Record;2016-03-10
5. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
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