том 33 издание 6 страницы 363-372

Modular Phospholane Ligands in Asymmetric Catalysis

Тип публикацииJournal Article
Дата публикации2000-03-21
scimago Q1
wos Q1
БС1
SJR5.433
CiteScore30.7
Impact factor17.7
ISSN00014842, 15204898
General Chemistry
General Medicine
Краткое описание
This Account outlines the preparation and application of a class of phosphine ligands based upon the trans-2,5-disubstituted phospholane moiety. The modular nature of these ligands has allowed facile variation of both phospholane substituent and backbone structure, thus providing access to a series of ligands. Bidentate bis(phospholane) ligands have been found to be very useful in asymmetric catalytic hydrogenation reactions. In particular, we highlight the versatility of highly efficient bis(phospholane)rhodium catalysts that allow enantioselective hydrogenation to produce a diverse range of compounds containing C-N, C-O, and C-C stereogenic centers.
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ГОСТ |
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Burk M. J. Modular Phospholane Ligands in Asymmetric Catalysis // Accounts of Chemical Research. 2000. Vol. 33. No. 6. pp. 363-372.
ГОСТ со всеми авторами (до 50) Скопировать
Burk M. J. Modular Phospholane Ligands in Asymmetric Catalysis // Accounts of Chemical Research. 2000. Vol. 33. No. 6. pp. 363-372.
RIS |
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TY - JOUR
DO - 10.1021/ar990085c
UR - https://pubs.acs.org/doi/10.1021/ar990085c
TI - Modular Phospholane Ligands in Asymmetric Catalysis
T2 - Accounts of Chemical Research
AU - Burk, Mark J
PY - 2000
DA - 2000/03/21
PB - American Chemical Society (ACS)
SP - 363-372
IS - 6
VL - 33
PMID - 10891054
SN - 0001-4842
SN - 1520-4898
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2000_Burk,
author = {Mark J Burk},
title = {Modular Phospholane Ligands in Asymmetric Catalysis},
journal = {Accounts of Chemical Research},
year = {2000},
volume = {33},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://pubs.acs.org/doi/10.1021/ar990085c},
number = {6},
pages = {363--372},
doi = {10.1021/ar990085c}
}
MLA
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Burk, Mark J.. “Modular Phospholane Ligands in Asymmetric Catalysis.” Accounts of Chemical Research, vol. 33, no. 6, Mar. 2000, pp. 363-372. https://pubs.acs.org/doi/10.1021/ar990085c.