71841-08-2

Upstream product

• 118495-28-6 5-(4'-methyl-3'-pentenyl)-2,3-dihydrofuran 
• 43161-11-1 5-iodo-2-methylpent-2-ene 
• 459-88-1 (E)-4,8-dimethylnona-3,7-dien-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 2270-59-9 1-bromo-4-methylpent-3-ene 

Downstream Products

• 71841-09-3 (E)-methyl 6,10-dimethyl-2-(phenylthio)-5,9-undecadienoate 
• 71841-10-6 (E)-2-(2-Benzyloxy-1-hydroxy-ethyl)-6,10-dimethyl-2-phenylsulfanyl-undeca-5,9-dienoic acid methyl ester 
• 71883-81-3 (2α,3β,5aα,7β,9aβ)-(+/-)-methyl 7-bromodecahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-3-(phenylthio)-1-benzoxepin-3-carboxylate 
• 71885-18-2 (2α,3β,5aβ,7α,9aα)-(+/-)-methyl 7-bromodecahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-3-(phenylthio)-1-benzoxepin-3-carboxylate 
• 71841-12-8 (2α,3α,5aβ,7α,9aα)-(+/-)-methyl 7-bromodecahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-3-(phenylthio)-1-benzoxepin-3-carboxylate 
• 71883-80-2 (2α,3α,5aα,7β,9aβ)-(+/-)-methyl 7-bromodecahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-3-(phenylthio)-1-benzoxepin-3-carboxylate 
• 71841-15-1 (2α,5aβ,7α,9aα)-(+/-)-methyl 7-bromo-2,5,5a,6,7,8,9,9a-octahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-1-benzoxepin-3-carboxylate 
• 71883-82-4 (2α,5aα,7β,9aβ)-(+/-)-methyl 7-bromo-2,5,5a,6,7,8,9,9a-octahydro-6,6,9a-trimethyl-2-<(phenylmethoxy)methyl>-1-benzoxepin-3-carboxylate 
• 71841-10-6 (E)-(2RS,1'RS)-methyl 6,10-dimethyl-2-<2'-(benzyloxy)-1'-hydroxyethyl>-2-(phenylthio)-5,9-undecadienoate 
• 71841-11-7 (E)-(2RS,1'SR)-methyl 6,10-dimethyl-2-<2'-(benzyloxy)-1'-hydroxyethyl>-2-(phenylthio)-5,9-undecadienoate 
• 81844-70-4 (3aα,4aβ,7β,8aα,10aβ)-(+/-)-7-bromodecahydro-4a,8,8-trimethyl-10a(phenylthio)furo<3,4-b><1>benzoxepin-1(3H)-one 
• 74144-04-0 (2(1')E,5E)-methyl 2-(2'-benzyloxyethylidene)-6,10-dimethyl-5,9-undecadienoate 
• 74144-05-1 (2(1')Z,5E)-methyl 2-(2'-benzyloxyethylidene)-6,10-dimethyl-5,9-undecadienoate 

Relevant academic research and scientific papers

Enantioselective synthesis of cyclic ethers through a vanadium-catalyzed resolution/oxidative cyclization

(Chemical Equation Presented) Two steps, one catalyst: A vanadium(v)-oxo complex with a tridentate Schiff base as an additional ligand catalyzes the title reaction which transforms racemic bishomoallylic α-hydroxyesters into trans-tetrahydropyrans (THPs)