860653-35-6

Upstream product

• 860653-32-3 1,1'-dibenzyl-2-(tert-butyldimethylsiloxy)-1H,1'H-[3,3']biindolyl 
• 860653-33-4 4-[(1,1'-dibenzyl-2-oxo-1,2-dihydro-1'H-[3,3']biindolyl-3-yl)hydroxymethyl]-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 860653-34-5 (S)-3-((1S,2R)-2-Amino-1,3-dihydroxy-propyl)-1,1'-dibenzyl-1,3-dihydro-1'H-[3,3']biindolyl-2-one 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 926011-01-0 (2S,3S,3aR,8aS)-8-Benzyl-3a-(1-benzyl-1H-indol-3-yl)-3-methoxy-1,2,3,3a,8,8a-hexahydro-pyrrolo[2,3-b]indole-2-carboxylic acid methylamide 
• 926010-99-3 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-2-hydroxymethyl-3-methoxy-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926010-98-2 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-3-hydroxy-2-hydroxymethyl-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926010-97-1 (2R,3S,3aR,8aS)-8-Benzyl-3a-(1-benzyl-1H-indol-3-yl)-3-isopropenyloxy-2-trimethylsilanyloxymethyl-1,2,3,3a,8,8a-hexahydro-pyrrolo[2,3-b]indole 
• 926011-00-9 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-3-methoxy-2-methylcarbamoyl-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926011-04-3 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-hydroxy-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926011-05-4 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methoxy-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926011-08-7 8-benzyl-3a-(1-benzyl-1H-indol-3-yl)-3-isopropenyloxy-2-trimethylsilanyloxymethyl-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid tert-butyl ester 
• 926010-96-0 9-benzyl-4b-(1-benzyl-1H-indol-3-yl)-3,3-dimethyl-4a,4b,9,9a,10,10a-hexahydro-1H-2,4-dioxa-9,10-diaza-indeno[1,2-a]indene 

Relevant academic research and scientific papers

Enantioselective total synthesis of (+)-gliocladin C

(Chemical Equation Presented) The first total synthesis of gliocladin C, a fungal-derived marine alkaloid containing a rare trioxopiperazine fragment, is reported. This asymmetric synthesis establishes the absolute configuration of this structurally novel

Asymmetric construction of quaternary carbon stereocenters: High stereoselection in Mukaiyama aldol reactions of 2-siloxyindoles with chiral aldehydes

(Chemical Equation Presented) A new synthesis of enantiopure 3,3-disubstituted oxindoles by stereoselective Mukaiyama aldol reaction of 3-substituted 2-siloxyindoles and chiral, enantiopure aldehydes having nitrogen or oxygen substituents at the α carbon