943589-85-3

Upstream product

• 943589-84-2 1,4-dimethoxycyclohexene 
• 150-76-5 4-methoxy-phenol 
• 69125-55-9 4-hydroxy-1-methoxy-1-cyclohexene 

Downstream Products

• 654667-51-3 2-bromo-4-methoxy-1-trifluoromethanesulfonyloxycyclohexene 
• 679788-47-7 tert-butyl (E)-(1''S,3a''R,7a''S)-3-[2'-(1''-tert-butoxy-7a''-methyl-2'',3'',3a'',6'',7'',7a''-hexahydro-1''H-inden-5''-yl)-5'-methoxycyclohex-1'-enyl]acrylate 
• 679788-54-6 (3S,3aS,7aS)-6-(2'-bromo-4'-methoxycyclohex-1'-enyl)-3-tert-butoxy-3a-methyl-2,3,3a,4,5,7a-hexahydro-1H-indene 
• 679788-46-6 (3S,3aS,7aR)-6-(2'-bromo-4'-methoxycyclohex-1'-enyl)-3-tert-butoxy-3a-methyl-2,3,3a,4,5,7a-hexahydro-1H-indene 

Relevant academic research and scientific papers

Stille-heck coupling sequences applied in a versatile new access to steroid skeletons

A variety of enantiomerically pure steroidal compounds was synthesized utilizing a sequence of Stille and Heck cross-coupling reactions and subsequent thermal 6π-electrocyclizations. Highly chemoselective Stille couplings on the triflate moiety of several