Synthesis of acyl halides under very mild conditions
Тип публикации: Journal Article
Дата публикации: 1979-01-01
SJR: —
CiteScore: —
Impact factor: —
ISSN: 00224936
Molecular Medicine
Краткое описание
On treatment with tetramethyl-α-halogenoenamines at room temperature or below, carboxylic acids are converted into acyl halides in high yields under neutral conditions.
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182
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182
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ГОСТ |
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ГОСТ
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Devos A. et al. Synthesis of acyl halides under very mild conditions // Journal of the Chemical Society Chemical Communications. 1979. Vol. 24. p. 1180.
ГОСТ со всеми авторами (до 50)
Скопировать
Devos A., Remion J., Frisque Hesbain A. M., Frisque-Hesbain A., Colens A., Ghosez L. Synthesis of acyl halides under very mild conditions // Journal of the Chemical Society Chemical Communications. 1979. Vol. 24. p. 1180.
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RIS
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TY - JOUR
DO - 10.1039/c39790001180
UR - https://doi.org/10.1039/c39790001180
TI - Synthesis of acyl halides under very mild conditions
T2 - Journal of the Chemical Society Chemical Communications
AU - Devos, Alain
AU - Remion, Jeanine
AU - Frisque Hesbain, Anne Marie
AU - Frisque-Hesbain, Anne-Marie
AU - Colens, Alain
AU - Ghosez, L.
PY - 1979
DA - 1979/01/01
PB - Royal Society of Chemistry (RSC)
SP - 1180
IS - 24
SN - 0022-4936
ER -
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BibTex (до 50 авторов)
Скопировать
@article{1979_Devos,
author = {Alain Devos and Jeanine Remion and Anne Marie Frisque Hesbain and Anne-Marie Frisque-Hesbain and Alain Colens and L. Ghosez},
title = {Synthesis of acyl halides under very mild conditions},
journal = {Journal of the Chemical Society Chemical Communications},
year = {1979},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c39790001180},
number = {24},
pages = {1180},
doi = {10.1039/c39790001180}
}