473980-86-8

Upstream product

• 100-52-7 benzaldehyde 
• 77118-87-7 (S)-1-Phenyl-3-buten-1-ol 
• 1347703-92-7 C₂₀H₂₅NO₄ 
• 1347703-91-6 C₁₄H₂₀O₄ 
• 1347703-90-5 C₁₁H₁₄O₃ 
• 1347703-89-2 C₁₂H₁₆O₂ 
• 1347704-00-0 C₃₀H₃₄O₆ 
• 1347703-99-4 C₂₇H₃₀O₅ 
• 1347703-94-9 C₂₈H₃₂O₄ 
• 474087-63-3 (4R,5R)-4-Phenyl-5-vinyl-[1,3]dioxolan-2-one 
• 145376-17-6 (1R,2R)-1-phenyl-but-3-ene-1,2-diol 
• 473980-85-7 (2Z,5E)-(S)-7-Hydroxy-7-phenyl-hepta-2,5-dienoic acid methyl ester 

Downstream Products

• 146236-73-9 (+)-goniodiol 

Relevant academic research and scientific papers

Tandem α-aminoxylation-allylation reaction based approach for the synthesis of goniothalesdiol A, leiocarpin A and (+)-goniodiol

A short and efficient syntheses of goniothalesdiol A, leiocarpin A, and (+)-goniodiol are reported by a convergent strategy using tandem aminoxylation-allylation reaction as a key step starting from benzaldehyde.

A short and general approach to the synthesis of styryllactones: (+)-Goniodiol, its acetates and β-trifluoromethyl derivative, (+)-7-epi-Goniodiol and (+)-9-deoxygoniopypyrone

(+)-Goniodiol, its acetates and β-trifluoromethyl derivative, (+)-7-epi-Goniodiol and (+)-9-deoxygoniopypyrone, the representatives of styryllactones have been synthesized in a short and general way. The key steps involve the regioselective asymmetric dihydroxylation and the palladium-catalyzed cross-coupling of cyclic allylic carbonate with vinyltributylstannane.