Literature DB >> 30417909

Synthesis and cycloaddition reactions of strained alkynes derived from 2,2'-dihydroxy-1,1'-biaryls.

Anish Mistry1, Richard C Knighton, Sam Forshaw, Zakaria Dualeh, Jeremy S Parker, Martin Wills.   

Abstract

A series of strained alkynes, based on the 2,2'-dihydroxy-1,1'-biaryl structure, were prepared in a short sequence from readily-available starting materials. These compounds can be readily converted into further derivatives including examples containing fluorescent groups with potential for use as labelling reagents. The alkynes are able to react in cycloadditions with a range of azides without the requirement for a copper catalyst, in clean reactions with no observable side reactions.

Entities:  

Year:  2018        PMID: 30417909     DOI: 10.1039/c8ob01768a

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


  2 in total

1.  Developing bioorthogonal probes to span a spectrum of reactivities.

Authors:  Sean S Nguyen; Jennifer A Prescher
Journal:  Nat Rev Chem       Date:  2020-07-21       Impact factor: 34.035

2.  A strained alkyne-containing bipyridine reagent; synthesis, reactivity and fluorescence properties.

Authors:  Sam Forshaw; Richard C Knighton; Jami Reber; Jeremy S Parker; Nikola P Chmel; Martin Wills
Journal:  RSC Adv       Date:  2019-11-06       Impact factor: 4.036

  2 in total

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