Literature DB >> 27030373

A mild preparation of alkynes from alkenyl triflates.

Xiaowen Yang1, Dimin Wu, Zhaohong Lu, Hongbin Sun, Ang Li.   

Abstract

We report herein a protocol for preparing alkynes from alkenyl triflates. Stoichiometric LiCl promotes this transformation in DMF at ambient temperature. A range of terminal and internal alkynes were obtained smoothly. A one-pot procedure of alkyne formation/Cu-mediated Huisgen cycloaddition was developed, which may find use in synthesizing natural product-based probes.

Entities:  

Year:  2016        PMID: 27030373     DOI: 10.1039/c6ob00345a

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


  2 in total

1.  Nickel-Catalyzed Conversion of Enol Triflates into Alkenyl Halides.

Authors:  Julie L Hofstra; Kelsey E Poremba; Alex M Shimozono; Sarah E Reisman
Journal:  Angew Chem Int Ed Engl       Date:  2019-09-19       Impact factor: 15.336

2.  NHC-BIAN-Cu(I)-Catalyzed Friedländer-Type Annulation of 2-Amino-3-(per)fluoroacetylpyridines with Alkynes on Water.

Authors:  Magdalena Dolna; Michał Nowacki; Oksana Danylyuk; Artur Brotons-Rufes; Albert Poater; Michał Michalak
Journal:  J Org Chem       Date:  2022-04-08       Impact factor: 4.198

  2 in total

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