Literature DB >> 23968232

Stereocontrolled synthesis of 1,3-diols from enones: cooperative Lewis base-mediated intramolecular carbonyl hydrosilylations.

Casey Medina1, Kyle P Carter, Michael Miller, Timothy B Clark, Gregory W O'Neil.   

Abstract

A streamlined synthesis of β-hydroxy ketone substrates has been developed to further investigate a recently discovered cooperative Lewis base-mediated intramolecular carbonyl hydrosilylation reaction. The synthesis features an enone β-borylation/oxidation sequence that has proven to be quite general and high-yielding. This has allowed for additional investigations into the diastereoselectivity of the hydrosilylation reaction through the preparation of important polyketide fragments.

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Year:  2013        PMID: 23968232     DOI: 10.1021/jo401293a

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


  2 in total

1.  Chemoselective Carbonyl Allylations with Alkoxyallylsiletanes.

Authors:  Paul Spaltenstein; Elizabeth J Cummins; Kelly-Marie Yokuda; Tim Kowalczyk; Timothy B Clark; Gregory W O'Neil
Journal:  J Org Chem       Date:  2019-03-13       Impact factor: 4.354

2.  Iodine-mediated rearrangements of diallylsilanes.

Authors:  Gregory W O'Neil; Elizabeth J Cummins
Journal:  Tetrahedron Lett       Date:  2017-07-11       Impact factor: 2.415

  2 in total

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