1362209-83-3

Upstream product

• 1362209-68-4 tert-butyl ((S)-2-((2R,5S,9S)-9-((p-methoxybenzyloxy)methoxy)-1-(2,2,2-trichloroacetyl)-1-azaspiro[4.4]non-6-en-2-yl)-1-phenylethyl)carbamate 
• 1362209-66-2 2,2,2-trichloro-N-((1S,5S)-1-(2-((4S,6S)-2,2-dioxido-4-phenyl-1,2,3-oxathiazinan-6-yl)ethyl)-5-(((p-methoxybenzyl)oxy)methoxy)cyclopent-2-en-1-yl)acetamide 
• 1362209-64-0 (R)-1-((1S,5S)-5-((p-methoxybenzyloxy)methoxy)-1-(2,2,2-trichloroacetamido)cyclopent-2-en-1-yl)-5-phenylpentan-3-yl sulfamate 
• 1362209-61-7 N-((1S,5S)-5-((p-methoxybenzyloxy)methoxy)-1-((R)-3-hydroxy-5-phenylpentyl)cyclopent-2-en-1-yl)-2,2,2-trichloroacetamide 
• 1362209-58-2 N-((1S,5S)-5-((4-methoxybenzyloxy)methoxy)-1-((R)-3-(tert-butyldimethylsilyloxy)-5-phenylpentyl)cyclopent-2-en-1-yl)-2,2,2-trichloroacetamide 
• 62098-62-8 C₉H₅Cl₃O₃ 
• 76598-95-3 4-acetoxy-3,5-dichlorobenzoic acid 
• 1362209-56-0 C₃₃H₄₆Cl₃NO₅Si 
• 1362209-54-8 (1S,4S)-4-((p-methoxybenzyloxy)methoxy)-3-((S)-3-(tert-butyldimethylsilyloxy)-5-phenylpentyl)cyclopent-2-enol 
• 1362209-51-5 C₂₅H₄₃BOSi 
• 1362209-81-1 (2'S,3aS,5'R,6aS)-tert-butyl 5'-((S)-2-(4-acetoxy-3,5-dichlorobenzamido)-2-phenylethyl)-2-oxo-1'-(2,2,2-trichloroacetyl)-3a,6a-dihydrospiro[cyclopenta[d]oxazole-6,2'-pyrrolidine]-3(2H)-carboxylate 
• 1362209-79-7 2,6-dichloro-4-(((S)-2-((2'S,3aS,5'R,6aS)-2-oxo-1'-(2,2,2-trichloroacetyl)-2,3,3a,6a-tetrahydrospiro[cyclopenta[d]oxazole-6,2'-pyrrolidin]-5'-yl)-1-phenylethyl)carbamoyl)phenyl acetate 
• 1362209-72-0 tert-butyl ((S)-2-((2'S,3aS,5'R,6aS)-2-oxo-1'-(2,2,2-trichloroacetyl)-2,3,3a,6a-tetrahydrospiro[cyclopenta[d]oxazole-6,2'-pyrrolidin]-5'-yl)-1-phenylethyl)carbamate 
• 1362209-70-8 tert-butyl ((S)-2-((2R,5S,9S)-9-(carbamoyloxy)-1-(2,2,2-trichloroacetyl)-1-azaspiro[4.4]non-6-en-2-yl)-1-phenylethyl)carbamate 

Relevant academic research and scientific papers

Total synthesis of (-)-kaitocephalin based on a rh-catalyzed c-h amination

A total synthesis of (-)-kaitocephalin, an ionotropic glutamate receptor antagonist, is accomplished in highly stereocontrolled manner via Overman rearrangement, rhodium-catalyzed benzylic C-H amination, pyrrolidine formation involving nucleophilic openin