Literature DB >> 30288542

Non-toxic cyanide sources and cyanating agents.

Alexander M Nauth1, Till Opatz.   

Abstract

The present review gives an overview over non-toxic cyanation agents and cyanide sources used in the synthesis of structurally diverse products containing the nitrile function. Nucleophilic as well as electrophilic agents/systems that transfer the entire CN-group were taken in consideration. Reactions in which a preexisting carbon functionality is transformed into a nitrile function by addition of nitrogen are however not covered here.

Entities:  

Year:  2018        PMID: 30288542     DOI: 10.1039/c8ob02140f

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


  5 in total

Review 1.  Nanostructured silicate catalysts for environmentally benign Strecker-type reactions: status quo and quo vadis.

Authors:  Vladimir V Kouznetsov; José G Hernández
Journal:  RSC Adv       Date:  2022-07-20       Impact factor: 4.036

2.  Synthesis of unsymmetrically tetrasubstituted pyrroles and studies of AIEE in pyrrolo[1,2-a]pyrimidine derivatives.

Authors:  Taian Li; Mong-Feng Chiou; Yajun Li; Changqing Ye; Min Su; Mengyu Xue; Xiaobin Yuan; Chuanchuan Wang; Wen-Ming Wan; Daliang Li; Hongli Bao
Journal:  Chem Sci       Date:  2022-04-20       Impact factor: 9.969

Review 3.  Recent advances and prospects in the palladium-catalyzed cyanation of aryl halides.

Authors:  Mohan Neetha; C M A Afsina; Thaipparambil Aneeja; Gopinathan Anilkumar
Journal:  RSC Adv       Date:  2020-09-11       Impact factor: 4.036

4.  A Cyaphide Transfer Reagent.

Authors:  Daniel W N Wilson; Stephanie J Urwin; Eric S Yang; Jose M Goicoechea
Journal:  J Am Chem Soc       Date:  2021-06-30       Impact factor: 15.419

5.  A biocompatible stapling reaction for in situ generation of constrained peptides.

Authors:  Richard Morewood; Christoph Nitsche
Journal:  Chem Sci       Date:  2020-11-04       Impact factor: 9.825

  5 in total

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