том 18 издание 27 страницы 8315-8319

Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles

Тип публикацииJournal Article
Дата публикации2012-06-04
scimago Q1
wos Q2
БС1
SJR0.981
CiteScore6.7
Impact factor3.7
ISSN09476539, 15213765
General Chemistry
Catalysis
Organic Chemistry
Краткое описание
The direct organocatalytic asymmetric cyclopropanation reaction of oxindoles by employing oxindoles as C1 synthon and bromonitroolefins as a convenient C2 synthon is described.
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ГОСТ |
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Dou X., Lu Y. Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles // Chemistry - A European Journal. 2012. Vol. 18. No. 27. pp. 8315-8319.
ГОСТ со всеми авторами (до 50) Скопировать
Dou X., Lu Y. Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles // Chemistry - A European Journal. 2012. Vol. 18. No. 27. pp. 8315-8319.
RIS |
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TY - JOUR
DO - 10.1002/chem.201200655
UR - https://doi.org/10.1002/chem.201200655
TI - Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles
T2 - Chemistry - A European Journal
AU - Dou, Xiaowei
AU - Lu, Yixin
PY - 2012
DA - 2012/06/04
PB - Wiley
SP - 8315-8319
IS - 27
VL - 18
PMID - 22674465
SN - 0947-6539
SN - 1521-3765
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2012_Dou,
author = {Xiaowei Dou and Yixin Lu},
title = {Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles},
journal = {Chemistry - A European Journal},
year = {2012},
volume = {18},
publisher = {Wiley},
month = {jun},
url = {https://doi.org/10.1002/chem.201200655},
number = {27},
pages = {8315--8319},
doi = {10.1002/chem.201200655}
}
MLA
Цитировать
Dou, Xiaowei, and Yixin Lu. “Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles.” Chemistry - A European Journal, vol. 18, no. 27, Jun. 2012, pp. 8315-8319. https://doi.org/10.1002/chem.201200655.