Literature DB >> 12323025

Rearrangements of haloalkynol derivatives of glucofuranose.

Maureen Blandino1, Edward McNelis.   

Abstract

Bromoalkynol derivatives of diacetone glucose undergo rearrangements to dihaloenol ethers contained in furo[3,4-b]furan cores when treated with halonium-producing reagents. [reaction: see text]

Entities:  

Year:  2002        PMID: 12323025     DOI: 10.1021/ol026422q

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

Review 1.  Electrophilic halogenations of propargyl alcohols: paths to α-haloenones, β-haloenones and mixed β,β-dihaloenones.

Authors:  Pakorn Bovonsombat; Punyanuch Sophanpanichkul; Satreerat Losuwanakul
Journal:  RSC Adv       Date:  2022-08-12       Impact factor: 4.036

2.  Anionic cascade reactions. One-pot assembly of (Z)-chloro-exo-methylenetetrahydrofurans from β-hydroxyketones.

Authors:  István E Markó; Florian T Schevenels
Journal:  Beilstein J Org Chem       Date:  2013-07-03       Impact factor: 2.883

  2 in total

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