The Asymmetric Piers Hydrosilylation
Тип публикации: Journal Article
Дата публикации: 2016-05-26
scimago Q1
wos Q1
БС1
SJR: 5.489
CiteScore: 24.4
Impact factor: 15.6
ISSN: 00027863, 15205126
PubMed ID:
27212565
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Краткое описание
An axially chiral, cyclic borane decorated with just one C6F5 group at the boron atom promotes the highly enantioselective hydrosilylation of acetophenone derivatives without assistance of an additional Lewis base (up to 99% ee). The reaction is an unprecedented asymmetric variant of Piers' B(C6F5)3-catalyzed carbonyl hydrosilylation. The steric congestion imparted by the 3,3'-disubstituted binaphthyl backbone of the borane catalyst as well as the use of reactive trihydrosilanes as reducing agents are keys to success.
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ГОСТ
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Süsse L., Hermeke J., Oestreich M. The Asymmetric Piers Hydrosilylation // Journal of the American Chemical Society. 2016. Vol. 138. No. 22. pp. 6940-6943.
ГОСТ со всеми авторами (до 50)
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Süsse L., Hermeke J., Oestreich M. The Asymmetric Piers Hydrosilylation // Journal of the American Chemical Society. 2016. Vol. 138. No. 22. pp. 6940-6943.
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RIS
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TY - JOUR
DO - 10.1021/jacs.6b03443
UR - https://doi.org/10.1021/jacs.6b03443
TI - The Asymmetric Piers Hydrosilylation
T2 - Journal of the American Chemical Society
AU - Süsse, Lars
AU - Hermeke, Julia
AU - Oestreich, Martin
PY - 2016
DA - 2016/05/26
PB - American Chemical Society (ACS)
SP - 6940-6943
IS - 22
VL - 138
PMID - 27212565
SN - 0002-7863
SN - 1520-5126
ER -
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BibTex (до 50 авторов)
Скопировать
@article{2016_Süsse,
author = {Lars Süsse and Julia Hermeke and Martin Oestreich},
title = {The Asymmetric Piers Hydrosilylation},
journal = {Journal of the American Chemical Society},
year = {2016},
volume = {138},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/jacs.6b03443},
number = {22},
pages = {6940--6943},
doi = {10.1021/jacs.6b03443}
}
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MLA
Скопировать
Süsse, Lars, et al. “The Asymmetric Piers Hydrosilylation.” Journal of the American Chemical Society, vol. 138, no. 22, May. 2016, pp. 6940-6943. https://doi.org/10.1021/jacs.6b03443.