60644-67-9Relevant articles and documents
Synthesis of taiwaniaquinoids via Nazarov triflation
Liang, Guangxin,Xu, Yue,Seiple, Ian B.,Trauner, Dirk
, p. 11022 - 11023 (2007/10/03)
A unified approach toward the taiwaniaquinoids that has yielded four natural products is described. A new variant of the Nazarov reaction with concomitant formation of an enol triflate serves as one of the key steps, considerably shortening the synthetic
Behavior of Carbonyl Ylide Generated from 3-Chloro-3-(p-nitrophenyl)diazirine and Acetone. 1,3-Dipolar Cycloaddition to Benzaldehyde and Epoxide Formation
Ibata, Toshikazu,Toyoda, Jiro,Liu, Michael T. H.
, p. 2135 - 2138 (2007/10/02)
A carbonyl ylide generated from 3-chloro-3-(p-nitrophenyl)diazirine and acetone either 1,3-dipolar cycloadds to benzaldehydes to afford 2,2-dimethyl-4-aryl-5-(p-nitrophenyl)dioxole or intramolecularly cyclizes to give 2-chloro-2-methyl-3-(p-nitrophenyl)-3