Literature DB >> 31596305

Application of copper(i) salt and fluoride promoted Stille coupling reactions in the synthesis of bioactive molecules.

Victor Lee1.   

Abstract

The Stille coupling between organostannanes and organohalides is an effective catalytic method for organic synthesis. Despite the ample amount of published results in this area, finding the optimal conditions for this transformation is often not straightforward. It was observed that this reaction could be accelerated with improved efficiency by the addition of a Cu(i) salt and fluoride. This review summarises the application of this simple protocol in the synthesis of natural products, their analogues and other biologically active molecules, from 2004 to 2018.

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Year:  2019        PMID: 31596305     DOI: 10.1039/c9ob01602c

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


  3 in total

Review 1.  Progress in the total synthesis of inthomycins.

Authors:  Bidyut Kumar Senapati
Journal:  Beilstein J Org Chem       Date:  2021-01-07       Impact factor: 2.883

2.  Recoverable Palladium-Catalyzed Carbon-Carbon Bond Forming Reactions under Thermomorphic Mode: Stille and Suzuki-Miyaura Reactions.

Authors:  Eskedar Tessema; Vijayanath Elakkat; Chiao-Fan Chiu; Zong-Lin Tsai; Ka Long Chan; Chia-Rui Shen; Han-Chang Su; Norman Lu
Journal:  Molecules       Date:  2021-03-05       Impact factor: 4.411

3.  Dyedauxiliary Groups, an Emerging Approach in Organic Chemistry. The Case of Arylazo Sulfones.

Authors:  Di Qiu; Chang Lian; Jinshan Mao; Maurizio Fagnoni; Stefano Protti
Journal:  J Org Chem       Date:  2020-10-06       Impact factor: 4.354

  3 in total

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