1454846-25-3Relevant academic research and scientific papers
Regioselective dehydrative intramolecular heteroannulation of β-allyl-β-hydroxy dithioesters: Facile and straightforward entry to 2H-thiopyrans
Chowdhury, Sushobhan,Chanda, Tanmoy,Koley, Suvajit,Ramulu, B. Janaki,Raghuvanshi, Keshav,Singh, Maya Shankar
supporting information, p. 914 - 918 (2014/01/23)
β-Allyl-β-hydroxy dithioesters have been employed in the synthesis of hitherto unreported and synthetically demanding 2H-thiopyrans via regioselective intramolecular annulation strategy. Lewis acid BF 3·Et2O efficiently mediates the
Y(OTf)3 catalyzed substitution dependent oxidative C(sp 3)-C(sp3) cleavage and regioselective dehydration of β-allyl-β-hydroxydithioesters: Alternate route to α,β- unsaturated ketones and functionalized dienes
Chowdhury, Sushobhan,Chanda, Tanmoy,Nandi, Ganesh Chandra,Koley, Suvajit,Janaki Ramulu,Pandey,Singh, Maya Shankar
supporting information, p. 8899 - 8903 (2013/09/23)
β-Allyl-β-hydroxydithioesters have been generated by the regioselective Grignard addition to the β-oxodithioesters. They have been successfully employed in selective C(sp3)-C(sp3) bond cleavage to construct α,β-unsaturated ketone res
