156767-62-3Relevant articles and documents
Asymmetric synthesis of chiral sulfoxides and sulfinimines by using N-sulfinylsultam
Oppolzer, Wolfgang,Froelich, Olivier,Wiaux-Zamar, Chantal,Bernardinelli, Gerald
, p. 2825 - 2828 (2007/10/03)
Bornane-10,2-sultam 1 is stereoselectively converted by DMAP-assisted sulfinylation to diastereomerically pure (2R)-N-[(R)-p-tolylsulfinyl]-bornane-10,2-sultam 2 in 77% yield. The crystalline sulfinylating agent 2 reacts with a variety of nucleophiles to afford sulfoxides 3 and sulfinimines 5 in excellent yields and enantioselectivities.
A Formal and Enantioselective Synthesis of (-)-Serricornin, the Sex Pheromone of the Cigarette Beetle (Lasioderma serricorne F.)
Fereira, J. Tercio B.,Marques, Jacqueline A.,Marino, J. P.
, p. 641 - 648 (2007/10/02)
A synthesis of (-)-Serricornin is described.The (4S,5S)-4-methyl-5-ethyl δ-valerolactone 8 has been synthesized with a high degree of enantioselectivity starting from (R)-(+)-(E)-1-propenyl p-tolylsulfoxide 2, having the enantioselective Marino's lactoniz