120883-52-5Relevant academic research and scientific papers
A Versatile Route to 2-Substituted Cyclic 1,3-Dienes via a Copper(I)-Catalyzed Cross-Coupling Reaction of Dienyl Triflates with Grignard Reagents
Karlstroem, A. Sofia E.,Roenn, Magnus,Thorarensen, Atli,Baeckvall, Jan-E.
, p. 2517 - 2522 (1998)
A general synthesis of 2-substituted cyclic 1,3-dienes in two steps from α,β-unsaturated ketones has been developed. Formation of a dien-2-yl triflate followed by a copper(I)-catalyzed cross-coupling reaction with a Grignard reagent gives 2-substituted dienes in fair to excellent yields. Alkyl, aryl, and allyl Grignard reagents can be used.
A Stereoselective Organopalladium Route toward Perhydrohistrionicotoxin
Tanner, David,Sellen, Mikael,Baeckvall, Jan-E.
, p. 3374 - 3378 (2007/10/02)
An efficient stereocontrolled route to the spirocyclic alkaloid perhydrohistrionicotoxin (2) is described.The readily available 2-substituted 1,3-cyclohexadiene 4 was converted regio- and stereoselectively to the chloro acetate 5 by using organopalladium methodology.Chemoselective SN2' displacement of the chloride via a copper-catalyzed Grignard reaction furnished 6, thus establishing the correct relative configuration at two adjacent centers.Further elaboration to the δ-amino alkene 10 was followed by a completely stereoselective iodocyclization reaction which yielded azaspirocycle 11.This compound was transformed to depentylperhydrohistrionicotoxin (3) in essentially one operation, thus completing a formal total synthesis of the title alkaloid.The overall yield of 3 from 4 was 23percent for nine operations.An alternative route to advanced intermediate 8 was also developed, the key step being the coupling of enol triflate 15 with the appropriate lithium organocuprate reagent.
