Literature DB >> 11300915

Organic synthesis methodology. Preparation and diastereoselective birch reduction-alkylation of 3-substituted 2-methyl-2,3-dihydroisoindol-1-ones.

Z Guo1, A G Schultz.   

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Year:  2001        PMID： 11300915     DOI： 10.1021/jo005693g

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


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  2 in total

1.  De novo Assembly of the Benzenoid Ring as a Core Strategy for Synthesis of the Isoindolinone Natural Products Isohericerin, Erinacerin A, and Sterenin A.

Authors:  Chenlong Zhu; Juntian Zhang; Thomas R Hoye
Journal:  Org Lett       Date:  2021-09-20       Impact factor: 6.072

2.  Crucial role of selenium in the virucidal activity of benzisoselenazol-3(2H)-ones and related diselenides.

Authors:  Magdalena Pietka-Ottlik; Piotr Potaczek; Egbert Piasecki; Jacek Mlochowski
Journal:  Molecules       Date:  2010-11-12       Impact factor: 4.411
  2 in total

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