volume 60 issue 6 pages 597-604

An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes

Publication typeJournal Article
Publication date2013-04-02
scimago Q3
wos Q3
SJR0.337
CiteScore3.4
Impact factor1.5
ISSN00094536, 21926549
General Chemistry
Abstract
A direct and much simpler way was developed for the diastereoselective synthesis of spiro cyclopropan-1,3′-oxindoles from indolin-2-one/N-protected indolin-2-ones and bromonitroalkene. The fused restrained cyclopropanes were obtained with high diastereomeric ratios (upto >99:1) and in reasonable to high isolated chemical yields (upto 94%).
Found 
Found 

Top-30

Journals

1
2
Organic and Biomolecular Chemistry
2 publications, 20%
Asian Journal of Organic Chemistry
1 publication, 10%
Chemistry - A European Journal
1 publication, 10%
Advanced Synthesis and Catalysis
1 publication, 10%
Organic Chemistry Frontiers
1 publication, 10%
Mendeleev Communications
1 publication, 10%
RSC Advances
1 publication, 10%
Chemical Reviews
1 publication, 10%
Synthesis
1 publication, 10%
1
2

Publishers

1
2
3
4
Royal Society of Chemistry (RSC)
4 publications, 40%
Wiley
3 publications, 30%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 publication, 10%
American Chemical Society (ACS)
1 publication, 10%
Georg Thieme Verlag KG
1 publication, 10%
1
2
3
4
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
10
Share
Cite this
GOST |
Cite this
GOST Copy
Roy S., Chen K. An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes // Journal of the Chinese Chemical Society. 2013. Vol. 60. No. 6. pp. 597-604.
GOST all authors (up to 50) Copy
Roy S., Chen K. An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes // Journal of the Chinese Chemical Society. 2013. Vol. 60. No. 6. pp. 597-604.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1002/jccs.201200557
UR - https://doi.org/10.1002/jccs.201200557
TI - An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes
T2 - Journal of the Chinese Chemical Society
AU - Roy, Suparna
AU - Chen, Kwun-Min
PY - 2013
DA - 2013/04/02
PB - Wiley
SP - 597-604
IS - 6
VL - 60
SN - 0009-4536
SN - 2192-6549
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2013_Roy,
author = {Suparna Roy and Kwun-Min Chen},
title = {An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes},
journal = {Journal of the Chinese Chemical Society},
year = {2013},
volume = {60},
publisher = {Wiley},
month = {apr},
url = {https://doi.org/10.1002/jccs.201200557},
number = {6},
pages = {597--604},
doi = {10.1002/jccs.201200557}
}
MLA
Cite this
MLA Copy
Roy, Suparna, and Kwun-Min Chen. “An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes.” Journal of the Chinese Chemical Society, vol. 60, no. 6, Apr. 2013, pp. 597-604. https://doi.org/10.1002/jccs.201200557.