849479-86-3

Upstream product

• 500548-53-8 tert-butyl (2S)-5-bromo-2-{[methoxy(methyl)-amino]carbonyl}indoline-1-carboxylate 
• 500548-52-7 1-tert-butyl 2-methyl (2S)-5-bromoindoline-1,2-dicarboxylate 
• 197460-36-9 methyl (S)-N-(tert-butoxycarbonyl)indoline-2-carboxylate 
• 141410-06-2 (S)-indoline-2-carboxylic acid methyl ester 
• 79815-20-6 (S)-indoline-2-carboxylic acid 
• 849479-97-6 tert-butyl (2S)-5-bromo-2-[(1R)-1-hydroxy-1-phenylethynyl-1-butyl]indoline-1-carboxylate 
• 849479-85-2 (R)-3-((S)-5-Bromo-2,3-dihydro-1H-indol-2-yl)-1-phenyl-hexan-3-ol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 586390-99-0 (2S)-2-[(1R)-1-hydroxy-1-((2-phenyl)ethyl)butyl]indoline-5-carboxylic acid allyl ester 
• 849480-38-2 (1R,9aS)-3,3-dimethyl-1-(2-phenyl)ethyl-1-propyl-9,9a-dihydro-1H-[1,3]oxazolo[3,4-a]indole-7-carboxylic acid allyl ester 
• 849480-37-1 3,3-dimethyl-1-phenethyl-1-propyl-9,9a-dihydro-1H-oxazolo[3,4-a]indole-7-carboxylic acid 

Relevant academic research and scientific papers

Stereospecific synthesis of 2,2,3-trisubstituted tetrahydroquinolines: Application to the total syntheses of benzastatin E and natural virantmycin

An efficient methodology for the synthesis of 2,2,3-trisubstituted tetrahydroquinolines has been developed, which involves the triphenylphosphine- CCl4-mediated stereospecific rearrangement of α,α- disubstituted indoline-2-methanols 15 to 2,2,3-trisubstituted tetrahydroquinolines 26. The rearrangement precursors 15 are readily prepared by the diastereoselective Grignard addition to 2-acylindolines 13. The total syntheses of (+)-benzastatin E (1) and natural virantmycin (2a) were accomplished utilizing this methodology. This rearrangement reaction might afford some chemical precedent for the biogenetic pathway of the benzastatin family.