148679-34-9Relevant academic research and scientific papers
Sulfo-click reaction via in situ generated thioacids and its application in kinetic target-guided synthesis
Namelikonda, Niranjan Kumar,Manetsch, Roman
supporting information; experimental part, p. 1526 - 1528 (2012/03/11)
Herein, we describe a practical, one-pot variant of the sulfo-click reaction, in which 9-fluorenylmethyl-protected thioesters are rapidly deprotected and reacted further with sulfonylazides to give N-acyl sulfonamides.
A FACILE ROUTE TO TETRAHYDROISOQUINOLINE ALKALOIDS VIA SULFOXIDE MEDIATED CYCLIZATION
Takano, Seiichi,Iida, Hirokazu,Inomata, Kohei,Ogasawara, Kunio
, p. 47 - 52 (2007/10/02)
A facile route to 1,2,3,4-tetrahydroisoquinoline framework has been developed by employing the sulfoxide mediated cyclization reaction.Utilizing the reaction developed some naturally occurring isoquinoline alkaloids have been synthesized.
