том 8 издание 26 страницы 6127-6130

Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions

Тип публикацииJournal Article
Дата публикации2006-11-23
scimago Q1
wos Q1
БС1
SJR1.235
CiteScore8.7
Impact factor5
ISSN15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
[Structure: see text] Highly enantioselective Friedel-Crafts alkylation of simple and aromatic ethers (4a-l) with 3,3,3-trifluoropyruvate (3) was accomplished by using chiral (4R,5S)-DiPh-BOX(1b)-Cu(OTf)2 complex (1 mol %) as a catalyst under solvent-free conditions. Excellent yields and enantioselectivities (90-93% ee, after recrystallization up to 99% ee) of the Friedel-Crafts alkylation products were obtained.
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ГОСТ |
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Zhao J. et al. Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions // Organic Letters. 2006. Vol. 8. No. 26. pp. 6127-6130.
ГОСТ со всеми авторами (до 50) Скопировать
Zhao J., Liu L., Sui Y., Liu Y., Wang D., Chen Y. Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions // Organic Letters. 2006. Vol. 8. No. 26. pp. 6127-6130.
RIS |
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TY - JOUR
DO - 10.1021/ol0626037
UR - https://doi.org/10.1021/ol0626037
TI - Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions
T2 - Organic Letters
AU - Zhao, Junling
AU - Liu, Li
AU - Sui, Yong
AU - Liu, Yu-Liang
AU - Wang, Dong
AU - Chen, Yong-Jun
PY - 2006
DA - 2006/11/23
PB - American Chemical Society (ACS)
SP - 6127-6130
IS - 26
VL - 8
PMID - 17165946
SN - 1523-7060
SN - 1523-7052
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2006_Zhao,
author = {Junling Zhao and Li Liu and Yong Sui and Yu-Liang Liu and Dong Wang and Yong-Jun Chen},
title = {Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions},
journal = {Organic Letters},
year = {2006},
volume = {8},
publisher = {American Chemical Society (ACS)},
month = {nov},
url = {https://doi.org/10.1021/ol0626037},
number = {26},
pages = {6127--6130},
doi = {10.1021/ol0626037}
}
MLA
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Zhao, Junling, et al. “Catalytic and Highly Enantioselective Friedel−Crafts Alkylation of Aromatic Ethers with Trifluoropyruvate under Solvent-Free Conditions.” Organic Letters, vol. 8, no. 26, Nov. 2006, pp. 6127-6130. https://doi.org/10.1021/ol0626037.