Literature DB >> 12967308

First cross-coupling reactions on tetrazines.

Zoltán Novák1, András Kotschy.   

Abstract

[reaction: see text] A series of substituted chlorotetrazines were reacted with different terminal alkynes under Sonogashira or Negishi coupling conditions to furnish alkynyl-tetrazines in good to moderate yield. The electron-donating properties of the substituent on the tetrazine core were found to have a significant influence on the success of the reaction. These results constitute the first cross-coupling reactions on tetrazines.

Entities:  

Year:  2003        PMID: 12967308     DOI: 10.1021/ol035312w

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6-Disubstituted Tetrazines from Carboxylic Ester Precursors.

Authors:  Yixin Xie; Yinzhi Fang; Zhen Huang; Amanda M Tallon; Christopher W Am Ende; Joseph M Fox
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-07       Impact factor: 15.336

2.  In situ synthesis of alkenyl tetrazines for highly fluorogenic bioorthogonal live-cell imaging probes.

Authors:  Haoxing Wu; Jun Yang; Jolita Šečkutė; Neal K Devaraj
Journal:  Angew Chem Int Ed Engl       Date:  2014-04-24       Impact factor: 15.336

3.  Installation of Minimal Tetrazines through Silver-Mediated Liebeskind-Srogl Coupling with Arylboronic Acids.

Authors:  William D Lambert; Yinzhi Fang; Subham Mahapatra; Zhen Huang; Christopher W Am Ende; Joseph M Fox
Journal:  J Am Chem Soc       Date:  2019-10-22       Impact factor: 15.419

4.  Green- to far-red-emitting fluorogenic tetrazine probes - synthetic access and no-wash protein imaging inside living cells.

Authors:  Achim Wieczorek; Philipp Werther; Jonas Euchner; Richard Wombacher
Journal:  Chem Sci       Date:  2016-10-21       Impact factor: 9.825

Review 5.  Overview of Syntheses and Molecular-Design Strategies for Tetrazine-Based Fluorogenic Probes.

Authors:  Sang-Kee Choi; Jonghoon Kim; Eunha Kim
Journal:  Molecules       Date:  2021-03-26       Impact factor: 4.411

  5 in total

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