Literature DB >> 11429911

Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrile oxides.

C Yip1, S Handerson, G K Tranmer, W Tam.   

Abstract

Efficient routes to the synthesis of norbornadiene-tethered nitrile oxides have been developed, and their intramolecular 1,3-dipolar cycloadditions were studied. The cycloadditions occurred in good yields for a variety of substrates and were found to be highly regio- and stereoselective, giving single regio- and stereoisomers in most cases.

Entities:  

Year:  2001        PMID: 11429911     DOI: 10.1021/jo005611o

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


  3 in total

1.  Ring expansion of substituted norbornadienes for the synthesis of mono- and disubstituted 2-azabicyclo[3.2.1]octadienes.

Authors:  Nova Emelda; Stephen C Bergmeier
Journal:  Tetrahedron Lett       Date:  2008-09-08       Impact factor: 2.415

2.  5,8-Dimeth-oxy-3,9-dimethyl-3a,4,9,9a-tetra-hydro-4,9-ep-oxy-naphtho-[2,3-d]isoxazole.

Authors:  Alan J Lough; Jaipal R Nagireddy; William Tam
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-04-12

3.  (3-Methyl-3a,4,7,7a-tetra-hydro-5H-4,7-methano-isoxazolo[4,5-d][1,2]oxazin-5-yl)(phen-yl)methanone.

Authors:  Alan J Lough; Jaipal R Nagireddy; William Tam
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-04-12
  3 in total

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