Literature DB >> 24256807

Nickel-mediated stereocontrolled synthesis of spiroketals via tandem cyclization-coupling of β-bromo ketals and aryl iodides.

Yu Peng1, Xiao-Bo Xu, Jian Xiao, Ya-Wen Wang.   

Abstract

A ketal-tether approach for the stereoselective synthesis of [5,5] and [5,6]-spiroketals based on reductive coupling catalyzed by the readily available Ni complex is demonstrated. Either an intermolecular or an intramolecular stereospecific cascade has been achieved as well.

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Year:  2014        PMID: 24256807     DOI: 10.1039/c3cc47780k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  5 in total

1.  Nickel-Catalyzed Dicarbofunctionalization of Alkenes.

Authors:  Xiaoxu Qi; Tianning Diao
Journal:  ACS Catal       Date:  2020-07-02       Impact factor: 13.084

2.  Mechanism of Ni-Catalyzed Reductive 1,2-Dicarbofunctionalization of Alkenes.

Authors:  Qiao Lin; Tianning Diao
Journal:  J Am Chem Soc       Date:  2019-10-28       Impact factor: 15.419

3.  Concise Synthesis of (+)-β- and γ-Apopicropodophyllins, and Dehydrodesoxypodophyllotoxin.

Authors:  Jian Xiao; Guangming Nan; Ya-Wen Wang; Yu Peng
Journal:  Molecules       Date:  2018-11-21       Impact factor: 4.411

4.  Ni-catalysed reductive arylalkylation of unactivated alkenes.

Authors:  Youxiang Jin; Chuan Wang
Journal:  Chem Sci       Date:  2018-12-04       Impact factor: 9.825

5.  Synthesis of Vicinal Carbocycles by Intramolecular Nickel-Catalyzed Conjunctive Cross-Electrophile Coupling Reaction.

Authors:  Kirsten A Hewitt; Claire A Herbert; Elizabeth R Jarvo
Journal:  Org Lett       Date:  2022-08-04       Impact factor: 6.072

  5 in total

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