Literature DB >> 11463264

Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrones.

G K Tranmer1, W Tam.   

Abstract

Efficient routes to the synthesis of norbornadiene-tethered nitrones have been developed, and their intramolecular 1,3-dipolar cycloadditions were studied. The cycloadditions occurred in moderate to 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: 11463264     DOI: 10.1021/jo015610b

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


  2 in total

1.  Microwave-assisted synthesis of substituted hexahydro-pyrrolo[3,2-c]quinolines.

Authors:  Michal Neuschl; Darek Bogdal; Milan Potacek
Journal:  Molecules       Date:  2007-01-24       Impact factor: 4.411

2.  Ruthenium-Catalyzed [2 + 2] versus Homo Diels-Alder [2 + 2 + 2] Cycloadditions of Norbornadiene and Disubstituted Alkynes: A DFT Study.

Authors:  Austin Pounder; Leanne D Chen; William Tam
Journal:  ACS Omega       Date:  2020-12-18
  2 in total

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