том 18 издание 24 страницы 6324-6327

Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion

Тип публикацииJournal Article
Дата публикации2016-12-01
scimago Q1
wos Q1
white level БС1
SJR1.235
CiteScore8.7
Impact factor5
ISSN15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
A palladium-catalyzed spirocyclization forming spirooxindoles and spirodihydrobenzofurans has been achieved. Mechanistic studies suggest that the transformation proceeds through sequential carbopalladation, C-H activation, and benzyne insertion. Both classes of spirocycles have been synthesized in good to excellent yields, and the procedure is readily scalable.
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ГОСТ |
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Yoon H. et al. Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion // Organic Letters. 2016. Vol. 18. No. 24. pp. 6324-6327.
ГОСТ со всеми авторами (до 50) Скопировать
Yoon H., Lossouarn A., Landau F., Petrone D. A. Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion // Organic Letters. 2016. Vol. 18. No. 24. pp. 6324-6327.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/acs.orglett.6b03213
UR - https://doi.org/10.1021/acs.orglett.6b03213
TI - Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion
T2 - Organic Letters
AU - Yoon, Hyung
AU - Lossouarn, Alexis
AU - Landau, Felicitas
AU - Petrone, David A.
PY - 2016
DA - 2016/12/01
PB - American Chemical Society (ACS)
SP - 6324-6327
IS - 24
VL - 18
PMID - 27978695
SN - 1523-7060
SN - 1523-7052
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2016_Yoon,
author = {Hyung Yoon and Alexis Lossouarn and Felicitas Landau and David A. Petrone},
title = {Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion},
journal = {Organic Letters},
year = {2016},
volume = {18},
publisher = {American Chemical Society (ACS)},
month = {dec},
url = {https://doi.org/10.1021/acs.orglett.6b03213},
number = {24},
pages = {6324--6327},
doi = {10.1021/acs.orglett.6b03213}
}
MLA
Цитировать
Yoon, Hyung, et al. “Pd-Catalyzed Spirocyclization via C–H Activation and Benzyne Insertion.” Organic Letters, vol. 18, no. 24, Dec. 2016, pp. 6324-6327. https://doi.org/10.1021/acs.orglett.6b03213.
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