Literature DB >> 23409831

Methylene acetal formation from 1,2- and 1,3-diols using an O,S-acetal, 1,3-dibromo-5,5-dimethylhydantoin, and BHT.

Tomohiro Maegawa1, Yasuyuki Koutani, Kazuki Otake, Hiromichi Fujioka.   

Abstract

A mild and efficient method for formation of methylene acetals from 1,2- and 1,3-diols using methoxymethylphenylsulfide, 1,3-dibromo-5,5-dimethylhydantoin (DBDMH), and dibutylhydroxytoluene (BHT) is described. The use of BHT in this process suppresses side reactions and enables high-yielding formation of methylene acetals of various diols, including carbohydrate-type substrates.

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Year:  2013        PMID: 23409831     DOI: 10.1021/jo4000256

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Practical Glucosylations and Mannosylations Using Anomeric Benzoyloxy as a Leaving Group Activated by Sulfonium Ion.

Authors:  Linlin Xing; Qun Niu; Chunbao Li
Journal:  ACS Omega       Date:  2017-07-18
  1 in total

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