CuI/l -Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds
Тип публикации: Journal Article
Дата публикации: 2005-09-23
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR: 1.007
CiteScore: 7.7
Impact factor: 4.7
ISSN: 15237060, 15237052
PubMed ID:
16209512
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
[reaction: see text] The arylation of ethyl acetoacetate, ethyl benzoyl acetate, and diethyl malonate under the catalysis of CuI/L-proline in DMSO proceeds smoothly at 40-50 degrees C in the presence of Cs2CO3 to provide the 2-aryl-1,3-dicarbonyl compounds in good yields. Both aryl iodides and aryl bromides are compatible with these reaction conditions.
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ГОСТ
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Xie X., Cai G., Ma D. CuI/l-Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds // Organic Letters. 2005. Vol. 7. No. 21. pp. 4693-4695.
ГОСТ со всеми авторами (до 50)
Скопировать
Xie X., Cai G., Ma D. CuI/l-Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds // Organic Letters. 2005. Vol. 7. No. 21. pp. 4693-4695.
Цитировать
RIS
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TY - JOUR
DO - 10.1021/ol0518838
UR - https://doi.org/10.1021/ol0518838
TI - CuI/l-Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds
T2 - Organic Letters
AU - Xie, Xiaoan
AU - Cai, Guorong
AU - Ma, Dawei
PY - 2005
DA - 2005/09/23
PB - American Chemical Society (ACS)
SP - 4693-4695
IS - 21
VL - 7
PMID - 16209512
SN - 1523-7060
SN - 1523-7052
ER -
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BibTex (до 50 авторов)
Скопировать
@article{2005_Xie,
author = {Xiaoan Xie and Guorong Cai and Dawei Ma},
title = {CuI/l-Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds},
journal = {Organic Letters},
year = {2005},
volume = {7},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/ol0518838},
number = {21},
pages = {4693--4695},
doi = {10.1021/ol0518838}
}
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MLA
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Xie, Xiaoan, et al. “CuI/l-Proline-Catalyzed Coupling Reactions of Aryl Halides with Activated Methylene Compounds.” Organic Letters, vol. 7, no. 21, Sep. 2005, pp. 4693-4695. https://doi.org/10.1021/ol0518838.
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