93605-99-3

Upstream product

• 93605-98-2 methyl (E,E,E)-2-methyl-7-hydroxy-15-(benzyloxy)pentadeca-2,8,10-trienoate 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 108586-13-6 (2E,8E,10E)-15-Benzyloxy-7-methoxymethoxy-2-methyl-pentadeca-2,8,10-trien-1-ol 
• 93606-02-1 (1R,2R,4aS,5S,8aR)-2-(4-Benzyloxy-butyl)-5-methoxymethoxy-1-methyl-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carbaldehyde 
• 93606-02-1 (1R,2R,4aS,5R,8aR)-2-(4-Benzyloxy-butyl)-5-methoxymethoxy-1-methyl-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carbaldehyde 
• 93606-02-1 1β-methyl-2α-(4-benzyloxybutyl)-5-(methoxymethoxy)-1,2,4aβ,5,6,7,8,8aα-octahydronaphthalene-1α-carboxaldehyde 
• 93606-00-9 (E,E,E)-2-methyl-7-(methoxymethoxy)-15-(benzyloxy)pentadeca-2,8,10-trienal 

Relevant academic research and scientific papers

Intramolecular Diels-Alder Cyclization of Conjugated Aldehydes. Synthesis of a Chlorothricolide Intermediate

Various substituted 2,8,10-undecatrienals have been found to undergo facile intramolecular Diels-Alder cyclization in the presence of dialkylaluminium chlorides to give bicyclooctahydronaphthalenecarboxaldehydes with high endo selectivity.The metho

DIELS-ALDER CYCLIZATION OF 2,8,10-UNDECATRIENALS AS A ROUTE TO 1,2,3,4,4a,5,6,8a-OCTAHYDRONAPHTHALENES

2,8,10-Undecatrienals have been found to undergo facile Diels-Alder cyclization upon treatment with alkylaluminum chlorides in methylene chloride at low temperature.The reaction is highly endo-selective.Protected alcohol substituents at the C-4 and C-7 po