869885-18-7

Upstream product

• 100-39-0 benzyl bromide 
• 26599-08-6 ethyl 3-phenyl-2-(triphenylphosphoranylidene)propanoate 
• 142-61-0 Hexanoyl chloride 

Downstream Products

• 1089678-87-4 5-benzyl-2-methyl-4-(2'-methyl-2'-propenyl)-1,5,6-undecatrien-4-ol 
• 1089678-76-1 4-allyl-5-benzyl-1,5,6-undecatrien-4-ol 
• 1070228-66-8 2-benzylocta-2,3-dien-1-ol 
• 1204199-69-8 ethyl 2-benzyl-3-methyl-3(Z)-octenoate 
• 1291073-75-0 C₂₇H₂₇ClN₂O₂ 
• 1291073-54-5 7-benzyl-9-(2,5-dichlorobenzoyl)-8-pentyl-1,2,3,4-tetrahydropyrido[1,2-a]pyrimidin-6-one 
• 1291073-65-8 5-benzyl-6-pentyl-1,2-dihydro-4H,7H-benzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione 
• 1291073-43-2 6-benzyl-8-(2-chlorobenzoyl)-7-pentyl-2,3-dihydroimidazo[1,2-a]pyridin-5(1H)-one 
• 1291073-61-4 5-benzyl-9-chloro-6-pentyl-1,2-dihydro-4H,7H-benzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione 
• 1291073-39-6 6-benzyl-8-(2,5-dichlorobenzoyl)-7-pentyl-2,3-dihydroimidazo[1,2-a]pyridin-5(1H)-one 
• 1291073-59-0 5-benzyl-10-chloro-6-pentyl-1,2-dihydro-4H,7H-benzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione 
• 1291073-37-4 6-benzyl-8-(2,4-dichlorobenzoyl)-7-pentyl-2,3-dihydroimidazo[1,2-a]pyridin-5(1H)-one 

Relevant academic research and scientific papers

Efficient preparation of 4-Iodofuran-2(5H)-ones by iodolactonisation of 2,3-allenoates with I2

4-Iodofuran-2(5H)-ones were prepared, in moderate to high yields, by the facile iodolactonisation of ethyl 2,3-allenoates with I2 in aqueous MeCN by the direct participation of the carbonyl oxygen atom in the regioselective electrophilic additi

Gold-catalyzed simultaneous formation of C-C, C=O, and C-F bonds in the presence of selectfluor: A synthesis of fluoroindenes from allene esters

An approach for the synthesis of fluorinated indene derivatives has been developed via a gold-catalyzed three-component tandem reaction between allene esters, Selectfluor, and water.

Ferric chloride hexahydrate-catalyzed highly regio- And stereoselective conjugate addition reaction of 2,3-allenoates with grignard reagents: An efficient synthesis of β,γ-alkenoates

Ferric chloride hexahydrate was shown to be an efficient catalyst for the conjugate addition of 2,3-allenoates with alkyl-, aryl-, or vinyl-Grignard reagents to synthesize polysubstituted β,γ-unsaturated alkenoates with high regio- and stereoselectivity.

Reaction of 2,3-allenoates with TsNBr2 in the presence of base: A facile highly stereoselective synthesis of (1E,2E)-3-bromo-4-oxo-N′- tosyl-2-alkenoxylimidic acid ethyl esters

(Chemical Equation Presented) A novel reaction pathway of 2,3-allenoates with an electrophile (TsNBr2) in the presence of K2CO 3 to produce (1E,2E)-3-bromo-4-oxo-N′-tosyl-2-alkenoxylimidic acid ethyl esters is reported. Th