Georg Thieme Verlag KG
Synthesis
,  издание 5 ,  страницы 681-684

Synthesis ofN-Benzhydrylamides from Nitriles by Ritter Reactions in Formic Acid

Тип публикации: Journal Article
Дата публикации: 2003-03-21
Georg Thieme Verlag KG
SCImago Q2
WOS Q2
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SJR: 0.443
CiteScore: 4.3
Impact factor: 2.2
ISSN: 00397881, 1437210X
Catalysis
Organic Chemistry
Краткое описание
Benzhydrol reacts with nitriles in refluxing formic acid to produce amides arising from the Ritter reaction. This reaction does not require a strong acid catalyst, and the products are isolated without the need for chromatography. The conditions permit the preparation of acrylamides and methacrylamides without polymerization of the nitrile.
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Lewis D. E., Lewis D. W. P. Synthesis ofN-Benzhydrylamides from Nitriles by Ritter Reactions in Formic Acid // Synthesis. 2003. Vol. 5. pp. 681-684.
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Lewis D. E., Lewis D. W. P. Synthesis ofN-Benzhydrylamides from Nitriles by Ritter Reactions in Formic Acid // Synthesis. 2003. Vol. 5. pp. 681-684.
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TY - JOUR
DO - 10.1055/s-2003-38069
UR - https://doi.org/10.1055/s-2003-38069
TI - Synthesis ofN-Benzhydrylamides from Nitriles by Ritter Reactions in Formic Acid
T2 - Synthesis
AU - Lewis, David E.
AU - Lewis, David W. P.
PY - 2003
DA - 2003/03/21
PB - Georg Thieme Verlag KG
SP - 681-684
IS - 5
SN - 0039-7881
SN - 1437-210X
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2003_Lewis,
author = {David E. Lewis and David W. P. Lewis},
title = {Synthesis ofN-Benzhydrylamides from Nitriles by Ritter Reactions in Formic Acid},
journal = {Synthesis},
year = {2003},
publisher = {Georg Thieme Verlag KG},
month = {mar},
url = {https://doi.org/10.1055/s-2003-38069},
number = {5},
pages = {681--684},
doi = {10.1055/s-2003-38069}
}
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