744266-48-6

Upstream product

• 744266-43-1 syn 3-benzoyl-oxy-4-phenyl-4-(3-tosylureido)-1-buten 
• 136693-03-3 (+)-1,1-dimethylethyl (N-((1S,2S)-2-hydroxy-1-phenyl-3-butenyl)amino)methanoate 
• 868703-12-2 Benzoic acid (S)-1-((S)-amino-phenyl-methyl)-allyl ester 
• 654639-86-8 Benzoic acid (S)-1-((S)-tert-butoxycarbonylamino-phenyl-methyl)-allyl ester 

Downstream Products

• 1027234-53-2 N-[1-(amino-phenyl-methyl)-allyl]-4-methyl-benzenesulfonamide 
• 928338-74-3 3-tert-butoxycarbonylamino-2-phenyl-piperidine-1-carboxylic acid tert-butyl ester 
• 928338-55-0 [1-phenyl-2-(toluene-4-sulfonylamino)-but-3-enyl]-carbamic acid tert-butyl ester 
• 928338-57-2 2-phenyl-3-(toluene-4-sulfonylamino)-3,4-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 928338-61-8 3-[tert-butoxycarbonyl-(2-methoxy-benzyl)-amino]-2-phenyl-piperidine-1-carboxylic acid tert-butyl ester 
• 928338-59-4 C₂₈H₃₈N₂O₆S 
• 136982-36-0 (2S,3S)-3-(2-methoxybenzylamino)-2-phenylpiperidine 

Relevant academic research and scientific papers

Asymmetric synthesis of (+)-CP-99,994 and (+)-L-733,060 from enantiomerically pure (3S,4S)-4-(tert-butylcarbamoyl)-4-phenyl-1-buten-3-ol

Asymmetric syntheses of neurokinin substance P receptor antagonists (+)-CP-99,994 and (+)-L-733,060 have been accomplished starting from enantiomerically pure (3S,4S)-4-(tert-butylcarbamoyl)-4-phenyl-1-buten-3-ol. Georg Thieme Verlag Stuttgart.

An efficient synthesis of optically active vicinal diamine arrays via palladium-catalyzed C-O to C-N bond transformation

Optically active vicinal diamine arrays have been provided efficiently via palladium-catalyzed C-O to C-N bond transformation.