NDLI: Lewis acid catalyzed cycloaddition of methylenecyclopropanes with salicylaldehydes.

Content Provider	Semantic Scholar
Author	Jiang, Min Shi, Min
Copyright Year	2010
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.
Starting Page	44
Ending Page	61
Page Count	18
File Format	PDF HTM / HTML
Alternate Webpage(s)	https://s3-eu-west-1.amazonaws.com/pstorage-acs-6854636/4458226/ol100814a_si_003.pdf
PubMed reference number	20462238v1
Alternate Webpage(s)	https://doi.org/10.1021/ol100814a
DOI	10.1021/ol100814a
Journal	Organic letters
Volume Number	12
Issue Number	11
Language	English
Access Restriction	Open
Subject Keyword	Fever Thioctic Acid indene
Content Type	Text
Resource Type	Article

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Lewis acid catalyzed cycloaddition of methylenecyclopropanes with salicylaldehydes.