Organic Chemistry Frontiers, volume 4, issue 1, pages 86-90
A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
Publication type: Journal Article
Publication date: 2017-01-01
Journal:
Organic Chemistry Frontiers
Q1
Q1
SJR: 1.016
CiteScore: 7.8
Impact factor: 4.6
ISSN: 20524110, 20524129
Organic Chemistry
Abstract
Trifluoromethylthiolation of methylenecyclopropanes (MCPs) has been developed by using AgSCF3/Na2S2O8as a trifluoromethylthiolation source (SCF3) to give trifluoromethylthiolated 1,2-dihydronaphthalene derivatives in moderate to good yields.
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Chen M. T. et al. A facile approach for the trifluoromethylthiolation of methylenecyclopropanes // Organic Chemistry Frontiers. 2017. Vol. 4. No. 1. pp. 86-90.
GOST all authors (up to 50)
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Chen M. T., Chen M., Tang X., Shi M. A facile approach for the trifluoromethylthiolation of methylenecyclopropanes // Organic Chemistry Frontiers. 2017. Vol. 4. No. 1. pp. 86-90.
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TY - JOUR
DO - 10.1039/c6qo00536e
UR - https://doi.org/10.1039/c6qo00536e
TI - A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
T2 - Organic Chemistry Frontiers
AU - Chen, Min Tao
AU - Chen, Min-Tao
AU - Tang, Xiang-Ying
AU - Shi, Min
PY - 2017
DA - 2017/01/01
PB - Royal Society of Chemistry (RSC)
SP - 86-90
IS - 1
VL - 4
SN - 2052-4110
SN - 2052-4129
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2017_Chen,
author = {Min Tao Chen and Min-Tao Chen and Xiang-Ying Tang and Min Shi},
title = {A facile approach for the trifluoromethylthiolation of methylenecyclopropanes},
journal = {Organic Chemistry Frontiers},
year = {2017},
volume = {4},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c6qo00536e},
number = {1},
pages = {86--90},
doi = {10.1039/c6qo00536e}
}
Cite this
MLA
Copy
Chen, Min Tao, et al. “A facile approach for the trifluoromethylthiolation of methylenecyclopropanes.” Organic Chemistry Frontiers, vol. 4, no. 1, Jan. 2017, pp. 86-90. https://doi.org/10.1039/c6qo00536e.