издание 2 страницы 237-240

The Formation of β-Lactam Derivatives through the Reaction of Dibenzoyl­acetylene and Aryl Isocyanates in the Presence of Trivalent Phosphorus Nucleophiles

Тип публикацииJournal Article
Дата публикации2004-01-21
SCImago Q2
WOS Q3
БС2
SJR0.443
CiteScore4.3
Impact factor2.2
ISSN00397881, 1437210X
Catalysis
Organic Chemistry
Краткое описание
An effective route to novel β-lactams is described. This involves reaction of dibenzoylacetylene and phenyl isocyanate or phenylsulfonyl isocyanate in the presence of trivalent phosphorus nucleophiles.
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ГОСТ |
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Yavari I., Alizadeh A. The Formation of β-Lactam Derivatives through the Reaction of Dibenzoyl­acetylene and Aryl Isocyanates in the Presence of Trivalent Phosphorus Nucleophiles // Synthesis. 2004. Vol. 2. pp. 237-240.
ГОСТ со всеми авторами (до 50) Скопировать
Yavari I., Alizadeh A. The Formation of β-Lactam Derivatives through the Reaction of Dibenzoyl­acetylene and Aryl Isocyanates in the Presence of Trivalent Phosphorus Nucleophiles // Synthesis. 2004. Vol. 2. pp. 237-240.
RIS |
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TY - JOUR
DO - 10.1055/s-2003-44386
UR - https://doi.org/10.1055/s-2003-44386
TI - The Formation of β-Lactam Derivatives through the Reaction of Dibenzoyl­acetylene and Aryl Isocyanates in the Presence of Trivalent Phosphorus Nucleophiles
T2 - Synthesis
AU - Yavari, Issa
AU - Alizadeh, Abdolali
PY - 2004
DA - 2004/01/21
PB - Georg Thieme Verlag KG
SP - 237-240
IS - 2
SN - 0039-7881
SN - 1437-210X
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2004_Yavari,
author = {Issa Yavari and Abdolali Alizadeh},
title = {The Formation of β-Lactam Derivatives through the Reaction of Dibenzoyl­acetylene and Aryl Isocyanates in the Presence of Trivalent Phosphorus Nucleophiles},
journal = {Synthesis},
year = {2004},
publisher = {Georg Thieme Verlag KG},
month = {jan},
url = {https://doi.org/10.1055/s-2003-44386},
number = {2},
pages = {237--240},
doi = {10.1055/s-2003-44386}
}
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