A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes
Тип публикации: Journal Article
Дата публикации: 2011-01-01
scimago Q1
wos Q2
БС1
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
21161095
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A new oxapalladacycle 3 can be conveniently prepared via direct ortho palladation of diphenylphosphinic acid with palladium acetate. Catalysts derived from 3 can efficiently catalyze Markovnikov-type additions of E-H bonds (P(O)-H, S-H and spC-H) to alkynes via a unique catalytic cycle.
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ГОСТ
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Xu Q. et al. A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes // Chemical Communications. 2011. Vol. 47. No. 8. pp. 2333-2335.
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Xu Q., Shen R., Ono Y., Nagahata R., SHIMADA S., Goto M., Han L. A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes // Chemical Communications. 2011. Vol. 47. No. 8. pp. 2333-2335.
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TY - JOUR
DO - 10.1039/C0CC03436C
UR - https://doi.org/10.1039/C0CC03436C
TI - A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes
T2 - Chemical Communications
AU - Xu, Qing
AU - Shen, Ruwei
AU - Ono, Yutaka
AU - Nagahata, Ritsuko
AU - SHIMADA, Shigeru
AU - Goto, Midori
AU - Han, Libiao
PY - 2011
DA - 2011/01/01
PB - Royal Society of Chemistry (RSC)
SP - 2333-2335
IS - 8
VL - 47
PMID - 21161095
SN - 1359-7345
SN - 1364-548X
ER -
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@article{2011_Xu,
author = {Qing Xu and Ruwei Shen and Yutaka Ono and Ritsuko Nagahata and Shigeru SHIMADA and Midori Goto and Libiao Han},
title = {A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes},
journal = {Chemical Communications},
year = {2011},
volume = {47},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/C0CC03436C},
number = {8},
pages = {2333--2335},
doi = {10.1039/C0CC03436C}
}
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MLA
Скопировать
Xu, Qing, et al. “A new oxapalladacycle generated via ortho C–H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E–H bonds to alkynes.” Chemical Communications, vol. 47, no. 8, Jan. 2011, pp. 2333-2335. https://doi.org/10.1039/C0CC03436C.