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B(C6F5)3 catalyzed direct nucleophilic substitution of benzylic alcohols: an effective method of constructing C–O, C–S and C–C bonds from benzylic alcohols†
Shan-Shui Meng,Qian Wang,Gong-Bin Huang,Li-Rong Lin,Jun-Ling Zhao,Albert S. C. Chan
RSC Advances Pub Date : 09/03/2018 00:00:00 , DOI:10.1039/C8RA05811C
Abstract

An efficient and general method of nucleophilic substitution of benzylic alcohols catalyzed by non-metallic Lewis acid B(C6F5)3 was developed. The reaction could be carried out under mild conditions and more than 35 examples of ethers, thioethers and triarylmethanes were constructed in high yields. Some bioactive organic molecules were synthesized directly using the methods.

Graphical abstract: B(C6F5)3 catalyzed direct nucleophilic substitution of benzylic alcohols: an effective method of constructing C–O, C–S and C–C bonds from benzylic alcohols
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