76511-78-9

Upstream product

• 5042-53-5 1-(phenylsulfanyl)acetone 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 

Downstream Products

• 91157-94-7 2,4-Dimethyl-5-(phenylthio)pyrimidine 
• 98816-01-4 (Z)-4-Acetoxy-3-phenylthio-3-buten-2-on 
• 98816-11-6 (E)-4-Acetoxy-3-phenylthio-3-buten-2-on 
• 131759-65-4 (2R^*,4R^*)-(+/-)-6-methyl-2,5-bis(phenylthio)-4-phthalimido-3,4-dihydro-2H-pyran 
• 110914-35-7 (2R^*,4R^*)-(+/-)-4-(acetyl-benzylamino)-2-ethoxy-6-methyl-5-(phenylthio)-3,4-dihydro-2H-pyran 
• 110914-35-7 (2R^*,4S^*)-(+/-)-4-(acetyl-benzylamino)-2-ethoxy-6-methyl-5-(phenylthio)-3,4-dihydro-2H-pyran 
• 131759-63-2 (2R^*,4S^*)-(+/-)-2-methoxy-6-methyl-5-(phenylthio)-4-phthalimido-3,4-dihydro-2H-pyran 
• 131759-63-2 (2R^*,4R^*)-(+/-)-2-methoxy-6-methyl-5-(phenylthio)-4-phthalimido-3,4-dihydro-2H-pyran 
• 110914-34-6 (2R^*,4S^*)-(+/-)-4-(benzoylamino)-2-ethoxy-6-methyl-5-(phenylthio)-3,4-dihydro-2H-pyran 
• 110914-34-6 (2R^*,4R^*)-(+/-)-4-(benzoylamino)-2-ethoxy-6-methyl-5-(phenylthio)-3,4-dihydro-2H-pyran 
• 131759-59-6 (E)-3-(phenylthio)-4-phthalamido-3-buten-2-one 
• 131759-60-9 4-(acetyl-benzylamino)-3-(phenylthio)-3-buten-2-one 
• 110914-26-6 4-(benzoylamino)-3-(phenylthio)-3-buten-2-one 
• 131759-57-4 4-ethoxy-3-(phenylthio)-3-buten-2-one 

Relevant academic research and scientific papers

De-novo Synthesis of Carbohydrates and Related Natural Products, 18. - Hetero-Diels-Alder Reactions for the Synthesis of 3,4-Dihydro-2H-pyrans

Hetero-Diels-Alder reactions between α,β-unsaturated carbonyl compounds with functional substituents in α- and β-position and enol ethers, enediol ethers, and ketene acetals, respectively, result in the formation of 3,4-dihydro-2H-pyrans 3, having functio

Synthesis of 2-Substituted 5-Acetyl-1(H)-imidazoles via 3-Chloro-4,4-dimethoxy-2-butanone and Related 3,4-Disubstituted 3-Buten-2-ones

A variety of 3,4-disubstituted 3-buten-2-ones have been synthesized and reacted with acetamidine to yield 5-acetyl-2-methyl-1(H)-imidazoles, 5-substituted pyrimidines, or both.The nature of the product depends on the substituents at position 3 and 4 of th