The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide
Тип публикации: Journal Article
Дата публикации: 1993-01-01
scimago Q2
wos Q2
БС2
SJR: 0.559
CiteScore: 4.6
Impact factor: 2.3
ISSN: 00397881, 1437210X
Catalysis
Organic Chemistry
Краткое описание
Due to the interest in tetrazoles as medicinal agents, a new, mild one-step method for the conversion of amides to tetrazoles employing triphenylphosphine, diethyl azodicarboxylate, and trimethylsilyl azide was recently introduced. An alternate and equally simple method employing trifluoromethanesulfonic anhydride and sodium azide was devised. This method was used to synthesize a series of 1,5-substituted tetrazoles from readily available secondary amides. A 1H-substituted tetrazole was also synthesized by this method from an amide substituted with a cyanoethyl protecting group
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Thomas E. W. The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide // Synthesis. 1993. Vol. 1993. No. 08. pp. 767-768.
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Thomas E. W. The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide // Synthesis. 1993. Vol. 1993. No. 08. pp. 767-768.
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TY - JOUR
DO - 10.1055/s-1993-25934
UR - https://doi.org/10.1055/s-1993-25934
TI - The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide
T2 - Synthesis
AU - Thomas, Edward W.
PY - 1993
DA - 1993/01/01
PB - Georg Thieme Verlag KG
SP - 767-768
IS - 08
VL - 1993
SN - 0039-7881
SN - 1437-210X
ER -
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@article{1993_Thomas,
author = {Edward W. Thomas},
title = {The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide},
journal = {Synthesis},
year = {1993},
volume = {1993},
publisher = {Georg Thieme Verlag KG},
month = {jan},
url = {https://doi.org/10.1055/s-1993-25934},
number = {08},
pages = {767--768},
doi = {10.1055/s-1993-25934}
}
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MLA
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Thomas, Edward W.. “The Conversion of Secondary Amides to Tetrazoles with Trifluoromethanesulfonic Anhydride and Sodium Azide.” Synthesis, vol. 1993, no. 08, Jan. 1993, pp. 767-768. https://doi.org/10.1055/s-1993-25934.