Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen
Publication type: Journal Article
Publication date: 1961-09-01
Inorganic Chemistry
Abstract
2.5-Diphenyl- und 2-Phenyl-5-methyl-tetrazol gehen bei 160°, 2-Methyl-5-phenyl-tetrazol bei 220° unter Stickstoffabgabe in die disubstituierten Nitrilimine uber. Als labile Zwischenstufen vermogen diese in situ primare und sekundare Amine, Thiophenole, Phenole und Carbonsauren zu addieren.
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99
Total citations:
99
Citations from 2024:
2
(2.02%)
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GOST
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HUISGEN R., Sauer J., Seidel M. Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen // Chemische Berichte. 1961. Vol. 94. No. 9. pp. 2503-2509.
GOST all authors (up to 50)
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HUISGEN R., Sauer J., Seidel M. Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen // Chemische Berichte. 1961. Vol. 94. No. 9. pp. 2503-2509.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/cber.19610940926
UR - https://doi.org/10.1002/cber.19610940926
TI - Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen
T2 - Chemische Berichte
AU - HUISGEN, Rolf
AU - Sauer, Jürgen
AU - Seidel, Michael
PY - 1961
DA - 1961/09/01
PB - Wiley
SP - 2503-2509
IS - 9
VL - 94
SN - 0009-2940
ER -
Cite this
BibTex (up to 50 authors)
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@article{1961_HUISGEN,
author = {Rolf HUISGEN and Jürgen Sauer and Michael Seidel},
title = {Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen},
journal = {Chemische Berichte},
year = {1961},
volume = {94},
publisher = {Wiley},
month = {sep},
url = {https://doi.org/10.1002/cber.19610940926},
number = {9},
pages = {2503--2509},
doi = {10.1002/cber.19610940926}
}
Cite this
MLA
Copy
HUISGEN, Rolf, et al. “Ringöffnungen der Azole, VI. Die Thermolyse 2.5‐disubstituierter Tetrazole zu Nitriliminen.” Chemische Berichte, vol. 94, no. 9, Sep. 1961, pp. 2503-2509. https://doi.org/10.1002/cber.19610940926.