Copper(II) Chloride Dihydrate: A Catalytic Agent for the Deprotection of Tetrahydropyranyl Ethers (THP Ethers) and 1-Ethoxyethyl Ethers (EE Ethers)

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Ammonium Decatungstocerate(IV): An Efficient Catalyst for the Protection and Deprotection of Tetrahydropyranyl Ethers

In multi-step organic syntheses, the protection and deprotection of tetrahydropyranyl (THP) ethers is one of the most frequently used methods. Over the years, different methods have been used from various catalytic systems for the protection of hydroxyl groups as THP ethers and their deprotection. Herein we have reported that various alcohols and phenols have been efficiently converted to the c...

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Chemoselective deprotection of triethylsilyl ethers.

An efficient and selective method was developed for the deprotection of triethylsilyl (TES) ethers using formic acid in methanol (5-10%) or in methylene chloride 2-5%) with excellent yields. TES ethers are selectively deprotected to the corresponding alcohols in high yields using formic acid in methanol under mild reaction conditions. Other hydroxyl protecting groups like t-butyldimethylsilyl (...

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ammonium decatungstocerate(iv): an efficient catalyst for the protection and deprotection of tetrahydropyranyl ethers

in multi-step organic syntheses, the protection and deprotection of tetrahydropyranyl (thp) ethers is one of the most frequently used methods. over the years, different methods have been used from various catalytic systems for the protection of hydroxyl groups as thp ethers and their deprotection. herein we have reported that various alcohols and phenols have been efficiently converted to the c...

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Deprotection of t-Butyldimethylsiloxy (TBDMS) Protecting Group with Catalytic Copper (II) Chloride Dihydrate

The protection of functional group is unavoidable in multi-step organic synthesis. Along with tetrahydropyranyl (THP) ethers, t-butyldimethylsilyl (TBDMS) ethers have been widely used for protecting hydroxyl groups. TBDMS ether is more stable to hydrolysis than trimethylsilyl ether, but is still readily cleaved by a variety of selective conditions. The deprotection of TBDMS is usually under mil...

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CLEAVAGE OF ESTERS AND ETHERS WITH SILICA CHLORIDE

Silica chloride converted benzyl or tert-butyl esters to the corresponding acid chlorides and alkyl chlorides. It also converted benzyl or tert-butyl phenyl ethers to the corresponding allcyl chlorides and phenol

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ژورنال

عنوان ژورنال: Journal of Chemical Research

سال: 1999

ISSN: 1747-5198,2047-6507

DOI: 10.1177/174751989902300424