Literature DB >> 22539254

Reductive azidation of carbonyl compounds via tosylhydrazone intermediates using sodium azide.

José Barluenga1, María Tomás-Gamasa, Carlos Valdés.   

Abstract

Entities:  

Year:  2012        PMID： 22539254     DOI： 10.1002/anie.201200313

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  3 in total

1.  N-Succinimidyl 3-((4-(4-[(18)F]fluorobutyl)-1H-1,2,3-triazol-1-yl)methyl)-5-(guanidinomethyl)benzoate ([(18)F]SFBTMGMB): a residualizing label for (18)F-labeling of internalizing biomolecules.

Authors:  Ganesan Vaidyanathan; Darryl McDougald; Jaeyeon Choi; Marek Pruszynski; Eftychia Koumarianou; Zhengyuan Zhou; Michael R Zalutsky
Journal:  Org Biomol Chem       Date:  2015-12-08       Impact factor: 3.876

2.  Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization.

Authors:  Lisa Moni; Luca Banfi; Andrea Basso; Alice Brambilla; Renata Riva
Journal:  Beilstein J Org Chem       Date:  2014-01-17       Impact factor: 2.883

3.  [2 + 2 + 1] Cycloaddition of N-tosylhydrazones, tert-butyl nitrite and alkenes: a general and practical access to isoxazolines.

Authors:  Liang Ma; Feng Jin; Xionglve Cheng; Suyan Tao; Gangzhong Jiang; Xingxing Li; Jinwei Yang; Xiaoguang Bao; Xiaobing Wan
Journal:  Chem Sci       Date:  2021-06-22       Impact factor: 9.825
  3 in total

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