3-Pyridinesulfonyl azide: A useful reagent for radical azidation

Advanced Synthesis and Catalysis

Volumn 346, Issue 8, 2004, Pages 925-928

  Panchaud, Philippe ^a   Renaud, Philippe ^a  

^a UNIVERSITY OF BERN   (Switzerland)

Author keywords

Amination; Azides; C C bond formation; Carboazidation; Radicals; Synthetic methods

Indexed keywords

AZIDE; CHLORIDE; PYRIDINE DERIVATIVE;

AMINATION; ANALYTIC METHOD; AQUEOUS SOLUTION; CHEMICAL MODIFICATION; CHEMICAL PROCEDURES; CHEMICAL REACTION; EXTRACTION; GEL; POLARIZATION; REACTION ANALYSIS; REVIEW; SYNTHESIS;

EID: 4344621526     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404038     Document Type: Review

References (11)

1. For a review, see: P. Panchaud, L. Chabaud, Y. Landais, C. Ollivier, P. Renaud, S. Zigmantas, Chem. Eur. J. 2004, 10, in press.
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11. Benzenesulfonyl azide and 3-pyridinesulfonyl azide are both stable liquids that start to decompose upon heating at 130°C (benzenesulfonyl azide) and 126°C (3-pyridinesulfonyl azide) according to a differential scanning calorimetry study.