Carbonyl ylides as possible intermediates in reactions of a mercurial dichlorocarbene precursor with benzaldehyde
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1971/C2/C29710001438
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Ylide formation of singlet carbene with carbonyl compound—laser flash photolysis of (biphenyl-4-yl)chlorodiazirine in propanone;Journal of Photochemistry and Photobiology A: Chemistry;2004-03
2. Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs;Chemical Reviews;1991-05
3. Behavior of Carbonyl Ylide Generated from 3-Chloro-3-(p-nitrophenyl)diazirine and Acetone. 1,3-Dipolar Cycloaddition to Benzaldehyde and Epoxide Formation;Chemistry Letters;1987-11-05
4. Dichlorocarbene from flash vacuum pyrolysis of trimethyl(trichloromethyl)silane. Possible observation of 1,1-dichloro-3-phenylcarbonyl ylide;The Journal of Organic Chemistry;1985-06
5. Divalent Carbon Transfer Reactions;Reactivity and Structure Concepts in Organic Chemistry;1985
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