издание 19 страницы 866

Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

Тип публикацииJournal Article
Дата публикации1979-01-01
SJR
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ISSN00224936
Molecular Medicine
Краткое описание
The reaction of aryl halides with alk-l-enylboranes, readily obtainable via monohydroboration of acetylenes, provides a conveninet new method for stereoselective synthesis of arylated (E)-alkenes in high yields; these reactions are effectively catalysed by tetrakis(triphenylphosphine)palladium and bases such as sodium ethoxide.
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ГОСТ |
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Miyaura N., Suzuki A. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst // Journal of the Chemical Society Chemical Communications. 1979. Vol. 19. p. 866.
ГОСТ со всеми авторами (до 50) Скопировать
Miyaura N., Suzuki A. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst // Journal of the Chemical Society Chemical Communications. 1979. Vol. 19. p. 866.
RIS |
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TY - JOUR
DO - 10.1039/c39790000866
UR - https://doi.org/10.1039/c39790000866
TI - Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
T2 - Journal of the Chemical Society Chemical Communications
AU - Miyaura, Norio
AU - Suzuki, Akira
PY - 1979
DA - 1979/01/01
PB - Royal Society of Chemistry (RSC)
SP - 866
IS - 19
SN - 0022-4936
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{1979_Miyaura,
author = {Norio Miyaura and Akira Suzuki},
title = {Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst},
journal = {Journal of the Chemical Society Chemical Communications},
year = {1979},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c39790000866},
number = {19},
pages = {866},
doi = {10.1039/c39790000866}
}
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