1574475-06-1

Upstream product

• 86867-62-1 (E)-3-(2-formylphenyl)propenoic acid ethyl ester 
• 643-79-8 o-phthalic dicarboxaldehyde 

Downstream Products

• 1574474-97-7 (R)-tert-butanesulfinylaldimine 
• 1574475-15-2 (R)-N-((1S,2R)-2-hydroxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide 
• 1574475-17-4 (R)-N-((1S,2R)-2-hydroxy-2-p-tolyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide 
• 1574475-18-5 (R)-N-((1S,2R)-2-hydroxy-2-m-tolyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide 
• 1574475-19-6 (R)-N-((1S,2R)-2-hydroxy-2-cyclohexanyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide 
• 1574475-21-0 (R)-N-((1S,2R)-2-hydroxy-2-benzyl-1,2,3,4-tetrahydronaphthalen-1-yl)tert-butylsulfinamide 
• 1574474-98-8 C₁₅H₂₁NO₂S 
• 1574475-07-2 C₁₄H₂₁NO₄ 
• 1574475-08-3 2-(3-oxo-3-phenylpropyl)benzaldehyde 
• 804553-24-0 2-(3-oxobutyl)benzaldehyde 
• 1574475-09-4 C₁₇H₁₆O₂ 
• 1574474-99-9 C₂₁H₂₅NO₂S 
• 1574475-10-7 C₁₇H₁₆O₂ 
• 1574475-11-8 C₁₆H₂₀O₂ 

Relevant academic research and scientific papers

Asymmetric synthesis of novel vicinal amino alcohols via intramolecular ketone- N -sulfinylimine pinacol-type reductive coupling promoted by SmI 2

A novel intramolecular asymmetric ketone-N-sulfinylimine pinacol-type reductive coupling reaction induced by SmI2 was reported. A series of 1-amino-1,2,3,4-tetrahydronaphthalen-2-carbinols were obtained in moderate to good yields with excellent