Literature DB >> 21105673

Stereodefined homopropargyl amines by tandem nucleophilic addition/fragmentation of dihydropyridone triflates.

Jumreang Tummatorn1, Gregory B Dudley.   

Abstract

Dihydropyridone (DHPD) triflates undergo nucleophile-triggered fragmentation to provide homopropargyl amine derivatives, the stereochemistry of which is defined by starting from readily available β-amino esters.

Entities:  

Year:  2010        PMID： 21105673     DOI： 10.1021/ol102760q

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


  2 in total

Review 1.  Computational studies on the regioselectivity of metal-catalyzed synthesis of 1,2,3 triazoles via click reaction: a review.

Authors:  Tayebeh Hosseinnejad; Bahareh Fattahi; Majid M Heravi
Journal:  J Mol Model       Date:  2015-09-18       Impact factor: 1.810

2.  A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals.

Authors:  Sami F Tlais; Gregory B Dudley
Journal:  Beilstein J Org Chem       Date:  2011-05-04       Impact factor: 2.883
  2 in total

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