845866-29-7Relevant academic research and scientific papers
Reactive Pt(II) center as part of redox-active quinoline-based heterocyclic scaffolds toward new anticancer leads
Kumbhakonam, Sateeshkumar,Saroj, Soumya,Venkatesan, Nalini,Devarajan, Karunagaran,Manheri, Muraleedharan K.
supporting information, (2020/10/12)
New cisplatin analogs in which the diamminedichloro-Pt(II) unit is conjugated to dihydroquinoline- or tetrahydroquinoline frameworks were synthesized and subjected to biological evaluation in order to understand their effects on cellular redox homeostasis
One-pot synthesis of allyl thioacetate from benzaldehydes and activated alkenes using the Morita-Baylis-Hillman reaction as a key step
Yang, Hae-Won,Choi, Ji-Su,Lee, Sang-Jin,Yoo, Byung-Woo,Yoon, Cheol Min
, p. 134 - 140 (2016/03/30)
An efficient, regioselective and steresoselecitive one-pot protocol for the synthesis of (Z)-S-2-alkoxycarbonyl-3-acylallyl ethanethioates and (E)-S-2-cyano-3-acylallyl ethanethioates from benzaldehydes and activated alkenes (methyl acrylate and acrylonit
Application of the acetate of Baylis-Hillman adducts in the synthesis of 3-carbomethoxy-2H-thiochromenes
Myeong, Jong Cha,Young, Seok Song,Han, Eun-Gu,Lee, Kee-Jung
, p. 235 - 240 (2008/09/19)
A new route to 2H-thiochromenes using the tandem SN2′ and SNAr reaction of several Baylis-Hillman acetates having an ortho-substituent, such as a halogen or nitro group, with sodium sulfide in aqueous dimethyl sulfoxide has been desc
Synthesis of methyl (E)-2-nitromethylcinnamates derived from baylis-hillman acetates and conversion into several coumarin derivatives
Hong, Wan Pyo,Lee, Kee-Jung
, p. 33 - 38 (2007/10/03)
Fast and easy access to methyl (E)-2-nitromethylcinnamates, from the corresponding Baylis-Hillman acetates with NaNO2 in DMF is described. Several ortho-chloro-2-nitromethylcinnamates undergo intramolecular aromatic substitution reaction follow
