843640-85-7Relevant academic research and scientific papers
An efficient synthesis of highly substituted pyrroles from β-oxodithiocarboxylates
Mathew, Paulson,Asokan
, p. 1708 - 1716 (2007/10/03)
α-Oxoketene-N,S-acetals, prepared by the reaction of alkyl glycinate hydrochlorides with β-oxodithiocarboxylates followed by alkylation, underwent cyclization in presence of chloromethyleneiminium salt derived from POCl3/DMF to afford alkyl-3-a
Cyclization of functionalized ketene-N,S-acetals to substituted pyrroles: Applications in the synthesis of marine pyrrole alkaloids
Mathew, Paulson,Asokan
, p. 475 - 478 (2007/10/03)
α-Oxoketene-N,S-acetals, prepared by the reaction of alkyl glycinates with β-oxodithiocarboxylates followed by alkylation, underwent cyclization in the presence of the Vilsmeier reagent to afford alkyl 3-aryl-4-formyl-5- (alkylsulfanyl)-1H-pyrrole-2-carbo
