Diastereodivergent Synthesis of 3‐Spirocyclopropyl‐2‐oxindoles through Direct Enantioselective Cyclopropanation of Oxindoles
Publication type: Journal Article
Publication date: 2012-06-04
scimago Q1
wos Q2
SJR: 0.981
CiteScore: 6.7
Impact factor: 3.7
ISSN: 09476539, 15213765
PubMed ID:
22674465
General Chemistry
Catalysis
Organic Chemistry
Abstract
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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Metrics
139
Total citations:
139
Citations from 2025:
6
(4.32%)
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MLA
Cite this
GOST
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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.
GOST all authors (up to 50)
Copy
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.
Cite this
RIS
Copy
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 -
Cite this
BibTex (up to 50 authors)
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@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}
}
Cite this
MLA
Copy
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.