951327-36-9

Upstream product

• 951327-34-7 C₁₄H₁₅BrO₅ 
• 107-30-2 chloromethyl methyl ether 
• 67451-62-1 cis-(1S,2S)-1,2-dihydroxy-3-bromocyclohexa-3,5-diene 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 

Downstream Products

• 951327-38-1 (1S,2S,5R,6S)-2-(4-methoxybenzyloxy)-3-bromo-5,6-bis(methoxymethoxy)cyclohex-3-enol 
• 951327-40-5 C₁₈H₂₄BrIO₆ 
• 951327-44-9 C₁₈H₂₅BrO₆ 
• 951327-46-1 C₁₀H₁₇BrO₅ 
• 951327-50-7 (3R,4S,6R)-6-azido-1-bromo-3,4-bis(methoxymethoxy)cyclohex-1-ene 
• 951327-53-0 (1R,4R,5S)-2-bromo-4,5-bis(methoxymethoxy)cyclohex-2-enamine 
• 951327-55-2 C₁₈H₂₆BrNO₅ 
• 951327-57-4 C₃₃H₃₆BrNO₈S 
• 951327-60-9 C₂₇H₃₁NO₈ 
• 951327-61-0 C₂₇H₃₃NO₇ 
• 951327-62-1 C₂₃H₂₅NO₅ 
• 951345-80-5 (1R,4R,5R,6R)-2-bromo-4,5,6-tris(methoxymethoxy)cyclohex-2-enamine 
• 951345-85-0 (1S,4R,5S)-2-bromo-4,5-bis(methoxymethoxy)cyclohex-2-enyl methanesulfonate 
• 951345-89-4 C₁₄H₂₁Cl₃BrNO₇ 

Relevant academic research and scientific papers

Chemoenzymatic approaches to the montanine alkaloids: A total synthesis of (+)-brunsvigine

The readily available and enzymatically derived cis-1,2-dihydrocatechols 3a and 3b have been elaborated over 17 steps, including a novel radical addition/elimination sequence, into the enantiomer, (+)-1, of the montanine alkaloid brunsvigine [(-)-1].

Chemoenzymatic approaches to lycorine-type amaryllidaceae alkaloids: Total syntheses of enf-lycoricidine, 3-epi-ent-lycoricidine, and 4-deoxy-3-epi-ent- lycoricidine

The readily available and enzymatically derived cis-1,2-dihydrocatechol 4 has been elaborated, over 11 steps including an Overman rearrangement, into the non-natural enantiomer, (-)-1, of the alkaloid lycoricidine [(+)-1]. Related chemistries have provided analogues 18, 19, and 26.