Literature DB >> 10814452

Benzhydryldimethylsilyl allylic silanes: syntheses and applications to

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Abstract

A new silyl group, the benzhydryldimethylsilyl group, has been developed that is easily synthesized and that undergoes facile oxidation. The [3 + 2] annulation reactions of allylic silanes with this silyl group provide a variety of highly substituted five-membered carbocycles and heterocycles with high stereoselectivities. The silyl groups of these cyclic compounds have been oxidized to hydroxyl groups to demonstrate the general synthetic utility of the method.

Year:  2000        PMID: 10814452     DOI: 10.1021/ol005676d

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


  4 in total

1.  Remote control of diastereoselectivity in intramolecular reactions of chiral allylsilanes.

Authors:  Weston R Judd; Sooho Ban; Jeffrey Aubé
Journal:  J Am Chem Soc       Date:  2006-10-25       Impact factor: 15.419

2.  Catalytic enantioselective carboannulation with allylsilanes.

Authors:  Nicolas R Ball-Jones; Joseph J Badillo; Ngon T Tran; Annaliese K Franz
Journal:  Angew Chem Int Ed Engl       Date:  2014-07-13       Impact factor: 15.336

3.  Triflimide-catalyzed allylsilane annulations of benzylic alcohols for the divergent synthesis of indanes and tetralins.

Authors:  Jordan C T Reddel; Weiwei Wang; Kalli Koukounas; Regan J Thomson
Journal:  Chem Sci       Date:  2016-12-09       Impact factor: 9.825

4.  Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes.

Authors:  Jing Li; Alexander Preinfalk; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2019-03-27       Impact factor: 15.336

  4 in total

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