1271726-69-2

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 70633-84-0 C₁₅H₂₀O₄ 
• 1271726-68-1 ethyl 2-((4R,6R)-2,2-dimethyl-6-((E)-styryl)-1,3-dioxan-4-yl)acetate 
• 735287-46-4 ethyl (E,R)-5-hydroxy-3-oxo-7-phenylhept-6-enoate 

Downstream Products

• 1271726-71-6 (E)-4-((4S,6R)-2,2-dimethyl-6-((E)-styryl)-1,3-dioxan-4-yl)but-2-enal 
• 1271726-72-7 C₂₁H₂₈O₃ 
• 1271726-73-8 C₂₄H₃₀O₄ 
• 160098-78-2 (6R)-5,6-dihydro-6-[(4'S*,6'R*,1'E,7'E)-4',6'-dihydroxy-8'-phenyl-1',7'-octadienyl]-2-pyrone 
• 1271726-70-5 C₂₀H₂₆O₄ 

Relevant academic research and scientific papers

Chemoenzymatic total synthesis of cryptocaryalactone natural products

A new chemoenzymatic route for the preparation of cryptocaryalactones natural products using a kinetic resolution process as the key step is described. Novozyme-435 catalyzed hydrolysis of the prochiral (±)-monoester 7 afforded the precursors of cryptocar

An efficient and stereoselective synthesis of obolactone via modified Evans' Aldol protocol

Stereocontrolled total synthesis of obolactone was achieved from trans-cinnamaldehyde. The key steps in this synthetic sequence are a asymmetric Mukaiyama Aldol, a Crimmins' modified Evans' Aldol reaction to introduce C2′ stereocentre, a nucleophilic addi

Total synthesis of (-)-diospongin A and (+)-cryptofolione via asymmetric aldol reaction

Stereoselective synthesis of two distinctive pyranone skeletons diospongin A and cryptofolione has been described based on an asymmetric aldol reaction starting from Chan's diene. The synthetic strategy involves the enantioselective Mukaiyama aldol, diast