82414-47-9

Upstream product

• 4364-06-1 (E)-cinnamaldehyde dimethylacetal 
• 72658-09-4 (E)-(1-methoxyprop-1-enyloxy)trimethylsilane 
• 14371-10-9 (E)-3-phenylpropenal 
• 5445-17-0 Methyl 2-bromopropionate 
• 77-78-1 dimethyl sulfate 
• 86853-06-7 Methyl 2-methyl-3-oxo-5-phenyl-4-pentenoate 
• 67498-12-8 (E)-(2S,3S)-3-Hydroxy-2-methyl-5-phenyl-pent-4-enoic acid methyl ester 
• 420-37-1 trimethoxonium tetrafluoroborate 
• 67498-12-8 (E)-syn-methyl 3-hydroxy-2-methyl-5-phenyl-4-pentanoate 

Downstream Products

• 88155-83-3 methyl (E)-(3R^*,4S^*)-4-methoxy-3-methyl-6-phenylhexa-5-enoate 
• 82414-48-0 (E)-(2S,3R)-3-Methoxy-2-methyl-5-phenyl-pent-4-enoic acid 
• 73341-71-6 (+/-)-oudemansin A 
• 73341-71-6 oudemansin A 

Relevant academic research and scientific papers

Efficient Activation of Acetals, Aldehydes, and Imines toward Silylated Nucleophiles by the Combined Use of Catalytic Amounts of 2 and TMS-CN under Almost Neutral Conditions

In the presence of catalytic amount of a transition metal compound such as 2, Co(acac)2, or NiCl2, trimethylsilyl cyanide smoothly reacts with acetals to form α-methoxy carbonitriles in good yields.In the coexistence of catalytic amounts of Rh