Literature DB >> 15281781

Palladium-catalyzed enantioselective ring opening of oxabicyclic alkenes with organozinc halides.

Ming Li1, Xiao-Xia Yan, Wei Hong, Xia-Zhen Zhu, Bo-Xun Cao, Jie Sun, Xue-Long Hou.   

Abstract

Palladium-catalyzed asymmetric ring opening of oxabenzonorbornadienes with readily available organozinc halides under mild conditions in the presence of (S)-Pr(i)-PHOX produces the corresponding 1,2-dihydronaphth-1-ols in good yield and high enantioselectivity. [reaction: see text]

Entities:  

Year:  2004        PMID： 15281781     DOI： 10.1021/ol048816i

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


  3 in total

1.  Oxa- and Azabenzonorbornadienes as Electrophilic Partners under Photoredox/Nickel Dual Catalysis.

Authors:  Youran Luo; Álvaro Gutiérrez-Bonet; Jennifer K Matsui; Madeline E Rotella; Ryan Dykstra; Osvaldo Gutierrez; Gary A Molander
Journal:  ACS Catal       Date:  2019-08-28       Impact factor: 13.084

2.  Iridium-catalyzed asymmetric ring-opening reactions of oxabicyclic alkenes with secondary amine nucleophiles.

Authors:  Dingqiao Yang; Ping Hu; Yuhua Long; Yujuan Wu; Heping Zeng; Hui Wang; Xiongjun Zuo
Journal:  Beilstein J Org Chem       Date:  2009-10-09       Impact factor: 2.883

3.  Regioselective palladium-catalyzed ring-opening reactions of C1-substituted oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates.

Authors:  Michael Edmunds; Mohammed Abdul Raheem; Rebecca Boutin; Katrina Tait; William Tam
Journal:  Beilstein J Org Chem       Date:  2016-02-09       Impact factor: 2.883
  3 in total

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