Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes
Тип публикации: Journal Article
Дата публикации: 1991-07-01
scimago Q3
wos Q3
БС2
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
Reaction of l-phenyl-1,3-butadiene with catecholborane in the presence of a rhodium catalyst beating triarylphosphine ligand such as PPh 3 or dppf proceeded regioselectively to give, after oxidation, anti -1-phenyl-1,3-butanediol in a good yield. Use of ( R ) BINAP as a chiral ligand for the catalytic hydroboration gave optically active (1 S ,3 R )-1-phenyl-1,3-butanediol of up to 67% ee.
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Matsumoto Y., Hayashi T. Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes // Tetrahedron Letters. 1991. Vol. 32. No. 28. pp. 3387-3390.
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Matsumoto Y., Hayashi T. Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes // Tetrahedron Letters. 1991. Vol. 32. No. 28. pp. 3387-3390.
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TY - JOUR
DO - 10.1016/S0040-4039(00)92714-X
UR - https://doi.org/10.1016/S0040-4039(00)92714-X
TI - Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes
T2 - Tetrahedron Letters
AU - Matsumoto, Yonetatsu
AU - Hayashi, Tamio
PY - 1991
DA - 1991/07/01
PB - Elsevier
SP - 3387-3390
IS - 28
VL - 32
SN - 0040-4039
SN - 1873-3581
ER -
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@article{1991_Matsumoto,
author = {Yonetatsu Matsumoto and Tamio Hayashi},
title = {Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes},
journal = {Tetrahedron Letters},
year = {1991},
volume = {32},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/S0040-4039(00)92714-X},
number = {28},
pages = {3387--3390},
doi = {10.1016/S0040-4039(00)92714-X}
}
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MLA
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Matsumoto, Yonetatsu, and Tamio Hayashi. “Asymmetric double hydroboration of 1,3-dienes catalyzed by chiral phosphine-rhodium complexes.” Tetrahedron Letters, vol. 32, no. 28, Jul. 1991, pp. 3387-3390. https://doi.org/10.1016/S0040-4039(00)92714-X.