2 Synthetic methods : Part (v) Protecting groups
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2003/OC/B212008A
Reference85 articles.
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2. Mild, aprotic synthesis of 1,2-diacetals
3. Tetrabutylammonium Tribromide (TBATB) as An Efficient Generator of HBr for an Efficient Chemoselective Reagent for Acetalization of Carbonyl Compounds
4. A Simple and Versatile Method for the Synthesis of Acetals from Aldehydes and Ketones Using Bismuth Triflate
5. Iodine-Catalyzed, Efficient and Mild Procedure for Highly Chemoselective Acetalization of Carbonyl Compounds under Neutral Aprotic Conditions
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1. o-Xylylene Protecting Group in Carbohydrate Chemistry: Application to the Regioselective Protection of a Single vic-Diol Segment in Cyclodextrins;The Journal of Organic Chemistry;2013-02-04
2. A Supramolecular Protecting Group Strategy Introduced to the Organic Solid State: Enhanced Reactivity through Molecular Pedal Motion;Angewandte Chemie International Edition;2011-12-12
3. A Supramolecular Protecting Group Strategy Introduced to the Organic Solid State: Enhanced Reactivity through Molecular Pedal Motion;Angewandte Chemie;2011-12-12
4. Metal-Dependent Reactions of Bulky Metal(II) Amides M[N(SiMe3)2]2 with 3,3′-Disubstituted Binaphthols (HO)2C20H10(SiR3)2-3,3′: Selective Conversion of One Equivalent −OH Group to a Silyl Ether −OSiMe3;Inorganic Chemistry;2008-01-18
5. Protective Group Strategies;The Organic Chemistry of Sugars;2005-09-21
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