Literature DB >> 24032575

Expedient and versatile formation of novel amino-deoxy-ketoheptuloses.

Yevgeniy Leshch1, Anna Jacobsen, Julian Thimm, Joachim Thiem.   

Abstract

Novel monoketoheptuloses have been synthesized employing an amination step in a pre- and/or post-C1 chain elongation using a Petasis reagent by starting from aldohexoses or aldohexosamines. A series of gluco and manno configured 1-/3-deoxy-1-/3-amino-ketohept-2-uloses could be obtained.

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Year:  2013        PMID: 24032575     DOI: 10.1021/ol4021699

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


  2 in total

Review 1.  Allylic azides: synthesis, reactivity, and the Winstein rearrangement.

Authors:  Angela S Carlson; Joseph J Topczewski
Journal:  Org Biomol Chem       Date:  2019-05-08       Impact factor: 3.876

2.  Synthesis of D-manno-heptulose via a cascade aldol/hemiketalization reaction.

Authors:  Yan Chen; Xiaoman Wang; Junchang Wang; You Yang
Journal:  Beilstein J Org Chem       Date:  2017-04-28       Impact factor: 2.883

  2 in total

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