Organic Letters, volume 12, issue 11, pages 2606-2609
Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes
Publication type: Journal Article
Publication date: 2010-05-12
Journal:
Organic Letters
Q1
Q1
SJR: 1.245
CiteScore: 9.3
Impact factor: 4.9
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Lewis acid catalyzed cycloaddition of methylenecyclopropanes (MCPs) with o-quinonemethide analogues, derived from the corresponding salicylaldehydes and CH(OEt)(3), produces the corresponding cycloadducts 3 in moderate to high yields at room temperature (20 degrees C). Moreover, the compounds 3 can be transformed to the indene derivatives 5 at high temperature. Plausible mechanisms have been proposed on the basis of control experiments.
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GOST
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Jiang M., Shi M. Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes // Organic Letters. 2010. Vol. 12. No. 11. pp. 2606-2609.
GOST all authors (up to 50)
Copy
Jiang M., Shi M. Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes // Organic Letters. 2010. Vol. 12. No. 11. pp. 2606-2609.
Cite this
RIS
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TY - JOUR
DO - 10.1021/ol100814a
UR - https://doi.org/10.1021/ol100814a
TI - Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes
T2 - Organic Letters
AU - Jiang, Min
AU - Shi, Min
PY - 2010
DA - 2010/05/12
PB - American Chemical Society (ACS)
SP - 2606-2609
IS - 11
VL - 12
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
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@article{2010_Jiang,
author = {Min Jiang and Min Shi},
title = {Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes},
journal = {Organic Letters},
year = {2010},
volume = {12},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/ol100814a},
number = {11},
pages = {2606--2609},
doi = {10.1021/ol100814a}
}
Cite this
MLA
Copy
Jiang, Min, and Min Shi. “Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes.” Organic Letters, vol. 12, no. 11, May. 2010, pp. 2606-2609. https://doi.org/10.1021/ol100814a.