116171-86-9

Upstream product

• 107688-28-8 3-benzyloxycarbonyl-7-benzyloxymethyl-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-9-carbonsauremethylester 
• 107688-23-3 2-benzyloxymethyl-2,3,4,5,6,7,8,13,13b-octahydro-1H-azepino<1',2':1,2>pyrido<3,4-b>indol 
• 107688-24-4 3-benzyloxycarbonyl-7-benzyloxymethyl-9-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol 
• 107688-24-4 3-benzyloxycarbonyl-7-benzyloxymethyl-9-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol 
• 107688-25-5 3-benzyloxycarbonyl-7-benzyloxymethyl-9-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydroazacyclo-undecino<5,4-b>indol 
• 107688-25-5 3-benzyloxycarbonyl-7-benzyloxymethyl-9-acetoxy-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol 
• 107688-27-7 3-benzyloxycarbonyl-7-benzyloxymethyl-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-7-carbonsaureamid 
• 107688-26-6 3-benzyloxycarbonyl-7-benzyloxymethyl-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-9-carbonsaurenitril 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 116171-87-0 3-benzyloxycarbonyl-7-benzyloxymethyl-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-9-carbonsaeurepentafuorophenylester 
• 116171-92-7 7-benzyloxymethyl-3,9-methano-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-15-on 
• 116171-94-9 C₂₅H₂₇ClN₂O₂ 
• 116171-93-8 7-benzyloxymethyl-9-(4-dimethylamino-2-methoxyphenyl)-3,9-methano-1,2,3,4,5,6,7,8,9,10-decahydroazacycloundecino<5,4-b>indol-15-on 

Relevant academic research and scientific papers

EINE NEUE SYNTHESE VON VINBLASTIN-DERIVATEN IV . SYNTHESE VON 20'-DEETHYL-20'-DEOXYVINBLASTIN und 20'-DEETHYL-20'-DEOXYVINCOVALIN UEBER 3,Nb-SECO-CLEAVAMIN-DERIVATIVE ALS ZWISCHENSTUFEN

Coupling of racemic 16-methoxycarbonyl-15,20-dihydro-3,Nb-seco-cleavamine derivative 34 with (-)vindoline via chloroindolenine intermediate 41 occurs with high stereoselectivity and leads after cyclization to the separable dimers 46I and 46II with natural C(14'), C(16')-configuration in good yields.Tetracyclic lactam 37 with vinblastine analogous stereochemistry is prepared and transfomed to chloroindolenine 38.Coupling of 38 with N,N-dimethyl-m-anisidine was achieved in good yield.