Reactions, which permit the selective deprotection of one silyl-protected alcohol in the
presence of another are reviewed. This review covers examples reported in the literature …

The widespread use of halogen‐based reagents in organic synthesis is well known.
Hypervalent halogens (oxidation states III and V) have been explored to a significant extent …

An environmentally benign PMA supported on SiO2 is found to be an efficient catalyst for the
chemoselective deprotection of TBDMS ethers under very mild conditions. Various labile …

The exploitation of reagents for the development new synthetic methods is an art and
constitutes a challenging process in organic chemistry. Consequently, considerable efforts …

Highly Chemoselective Esterification Reactions and Boc/THP/TBDMS Discriminating
Deprotections under Samarium(III) Catalysis | Organic Letters ACS ACS Publications C&EN …

A novel microwave-assisted, chemoselective and efficient method for the cleavage of silyl
ethers (aliphatic and aromatic) catalyzed by Selectfluor is reported. A wide range of TBS …

Selective deprotection of alkyl TBDMS ether in the presence of phenolic TBDMS ether using
dicationic ionic liquid [tetraEG (mim) 2][OMs] 2 as a homogeneous catalyst showed …

A high loading sulfonic acid-functionalized ordered nanoporous silica efficiently catalyzes
the deprotection of a variety of alcoholic TBDMS (tert-butyldimethylsilyl) ethers in methanol …

N-halosuccinimides (NXSs) are well-known to be convenient, easily manipulable and low-
priced halogenation reagents in organic synthesis. In the present work, N-bromosuccinimide …

N-Phthaloylchitosan represents a key intermediate for the regioselective modification of
chitosan in organic media. Chemoselective protection of primary alcohols on N …