Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds
Publication type: Journal Article
Publication date: 2010-12-16
scimago Q1
wos Q2
SJR: 0.981
CiteScore: 6.7
Impact factor: 3.7
ISSN: 09476539, 15213765
PubMed ID:
21268160
General Chemistry
Catalysis
Organic Chemistry
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GOST
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Su C. et al. Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds // Chemistry - A European Journal. 2010. Vol. 17. No. 5. pp. 1579-1585.
GOST all authors (up to 50)
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Su C., Cao J., Huang X., Wu L., Huang X. Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds // Chemistry - A European Journal. 2010. Vol. 17. No. 5. pp. 1579-1585.
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RIS
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TY - JOUR
DO - 10.1002/chem.201002141
UR - https://doi.org/10.1002/chem.201002141
TI - Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds
T2 - Chemistry - A European Journal
AU - Su, C
AU - Cao, J
AU - Huang, X
AU - Wu, L
AU - Huang, X
PY - 2010
DA - 2010/12/16
PB - Wiley
SP - 1579-1585
IS - 5
VL - 17
PMID - 21268160
SN - 0947-6539
SN - 1521-3765
ER -
Cite this
BibTex (up to 50 authors)
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@article{2010_Su,
author = {C Su and J Cao and X Huang and L Wu and X Huang},
title = {Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds},
journal = {Chemistry - A European Journal},
year = {2010},
volume = {17},
publisher = {Wiley},
month = {dec},
url = {https://doi.org/10.1002/chem.201002141},
number = {5},
pages = {1579--1585},
doi = {10.1002/chem.201002141}
}
Cite this
MLA
Copy
Su, C., et al. “Regiocontrolled Halohydroxylations of Bicyclic Vinylidenecyclopropanes: A Versatile Strategy for the Construction of Diverse Highly Functionalized Carbocyclic Scaffolds.” Chemistry - A European Journal, vol. 17, no. 5, Dec. 2010, pp. 1579-1585. https://doi.org/10.1002/chem.201002141.