102368-35-4

Upstream product

• 57137-74-3 (E)-4-methyl-2-(triethylsilyloxy)pent-2-ene 
• 102368-47-8 2-Dimethoxymethyl-4,5-diphenyl-oxazole 
• 102368-34-3 4,5-diphenyl-oxazole-2-carbaldehyde 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 14224-99-8 2-methyl-4,5-diphenyloxazole 
• 102368-48-9 3-[(4,5-Diphenyl-oxazol-2-yl)-methoxy-methyl]-4-methyl-pentan-2-one 

Downstream Products

• 124771-33-1 (E)-2-isopropyl-3-methyl-3-hydroxy-4-<(methoxymethyl)oxy>-1-(4,5-diphenyloxazol-2-yl)-1,4,5-hexatriene 
• 102368-43-4 4-(4,5-Diphenyl-oxazol-2-yl)-3-isopropyl-2-methyl-5-methylene-cyclopent-2-enone 

Relevant academic research and scientific papers

CATIONIC CYCLOPENTANNELATION. SYNTHESIS OF (d,l)-XANTHOCIDIN

A cationic cyclopentannelation reaction has been used for the key step of a concise synthesis of (d,l)-xanthocidin.An improvement on our previously described procedure for the preparation of 9 is reported.

Cationic Cyclopentaannelation: An Efficient Methylenomycin Synthesis

A cationic cyclopentaannelation reaction which was discovered in our laboratories has been used for an extremely short and efficient synthesis of some methylenomycins.Methylenomycin B was prepared in two steps. (+/-)-Desepoxy-4,5-didehydromethylenomycin A