Literature DB >> 23229014

Iridium-catalyzed asymmetric hydroalkynylation reactions of oxabenzonorbornadienes.

Jun Hu1, Qingjing Yang, Jianbin Xu, Chao Huang, Baomin Fan, Jun Wang, Chengyuan Lin, Zhaoxiang Bian, Albert S C Chan.   

Abstract

Oxabenzonorbornadienes were found to be suitable substrates for asymmetric hydroalkynylation reactions. Catalyzed by the complex of [Ir(COD)Cl](2) and (R)-SYNPHOS, oxabenzonorbornadienes and terminal alkynes could react smoothly to give the alkynylated products in moderate to good yields (up to 93% yield) and enantioselectivities (up to 85% ee).

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Year:  2012        PMID: 23229014     DOI: 10.1039/c2ob26775f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Gold-catalyzed reaction of oxabicyclic alkenes with electron-deficient terminal alkynes to produce acrylate derivatives.

Authors:  Yin-Wei Sun; Qin Xu; Min Shi
Journal:  Beilstein J Org Chem       Date:  2013-10-01       Impact factor: 2.883

  1 in total

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