том 18 издание 2 страницы 265-270

Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide

Тип публикацииJournal Article
Дата публикации2007-02-22
SJR
CiteScore
Impact factor
ISSN09574166, 1362511X
Catalysis
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
An organocatalyst derived from trans-4-hydroxy- l -proline and (1S,2S)-1,2-diphenyl-2-aminoethanol catalyzes the direct aldol reactions of cycloketones with a wide scope of aldehydes in high yields and with excellent diastereoselectivities of up to >99:1 and enantioselectivities of up to >99% ee.
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ГОСТ |
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He L. et al. Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide // Tetrahedron Asymmetry. 2007. Vol. 18. No. 2. pp. 265-270.
ГОСТ со всеми авторами (до 50) Скопировать
He L., Jiang J., TANG Z., Cui X., Mi A., Jiang Y., Gong L. Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide // Tetrahedron Asymmetry. 2007. Vol. 18. No. 2. pp. 265-270.
RIS |
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TY - JOUR
DO - 10.1016/j.tetasy.2007.01.028
UR - https://doi.org/10.1016/j.tetasy.2007.01.028
TI - Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide
T2 - Tetrahedron Asymmetry
AU - He, Long
AU - Jiang, Jun
AU - TANG, ZHUO
AU - Cui, Xin
AU - Mi, Ai-Qiao
AU - Jiang, Yao-Zhong
AU - Gong, Liu-Zhu
PY - 2007
DA - 2007/02/22
PB - Elsevier
SP - 265-270
IS - 2
VL - 18
SN - 0957-4166
SN - 1362-511X
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2007_He,
author = {Long He and Jun Jiang and ZHUO TANG and Xin Cui and Ai-Qiao Mi and Yao-Zhong Jiang and Liu-Zhu Gong},
title = {Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide},
journal = {Tetrahedron Asymmetry},
year = {2007},
volume = {18},
publisher = {Elsevier},
month = {feb},
url = {https://doi.org/10.1016/j.tetasy.2007.01.028},
number = {2},
pages = {265--270},
doi = {10.1016/j.tetasy.2007.01.028}
}
MLA
Цитировать
He, Long, et al. “Highly diastereo- and enantioselective direct aldol reactions of cycloketones with aldehydes catalyzed by a trans-4-tert-butyldimethylsiloxy-l-proline amide.” Tetrahedron Asymmetry, vol. 18, no. 2, Feb. 2007, pp. 265-270. https://doi.org/10.1016/j.tetasy.2007.01.028.