245760-13-8

Basic information

• Product Name: C₂₉H₃₆N₂O₄
• Synonyms: C₂₉H₃₆N₂O₄
• CAS NO: 245760-13-8
• Molecular Weight: 476.616
• Mol File: 245760-13-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₂₉H₃₆N₂O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₉H₃₆N₂O₄(245760-13-8)
• EPA Substance Registry System: C₂₉H₃₆N₂O₄(245760-13-8)

Safety Data

• Hazardous Substances Data: 245760-13-8(Hazardous Substances Data)

Upstream product

• 217448-27-6 (6S,10S)-8-(1'-ethyl-2'-propenyl)-9-(2',5'-dioxacyclopentanyl)-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctaindole 
• 217448-24-3 (6S,10S)-(-)-9-formyl-12-benzyl-6,7,10,11-tetrahydro-6,10-imino-5H-cyclooctaindole 
• 197143-13-8 (6S,10S)-(-)-9-oxo-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cycloocta[b]indole 
• 84094-74-6 (1S,3R)-(-)-methyl 2-benzyl-3-methoxycarbonyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-1-propionate 
• 63229-68-5 D-(+)-N_bbenzyltryptophan methyl ester 
• 100-52-7 benzaldehyde 
• 4299-70-1 D-Tryptophan methyl ester 
• 217448-26-5 (6S,10S)-8-(1'-ethyl-2'-propenyl)-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctaindole-9-carboxaldehyde 
• 913556-71-5 C₂₈H₂₆N₂O₂S 
• 217448-25-4 (6S,10S)-9-(1'-hydroxy-3'-hexenyl)-12-benzyl-6,7,10,11-tetrahydro-6,10-imino-5H-cyclooctaindole 
• 217448-33-4 (6S,10S)-8-(1'-ethyl-2'-propenyl)-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctaindole-9-carboxaldehyde 

Downstream Products

• 217448-31-2 (6S,13S)-4-ethyl-6,7,12,13-tetrahydro-14-(phenylmethyl)-6,13-imino-5H-pyrido[3',4':5,6]cyclooct[1,2-b]indole 
• 217448-29-8 C₂₆H₂₈N₂O₂ 
• 217448-28-7 (6S,10S)-8-(1'-ethyl-2'-acetyl)-9-(2',5'-dioxacyclopentanyl)-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctaindole 

Relevant articles and documents

General approach for the synthesis of ajmaline/sarpagine indole alkaloids: Enantiospecific total synthesis of (+)-ajmaline, alkaloid G, and norsuaveoline via the asymmetric Pictet-Spengler reaction

A general approach (oxyanion-Cope strategy) for the synthesis of sarpagine/ajmaline indole alkaloids has been developed. (+)-Ajmaline 1 and alkaloid G 2 as well as norsuaveoline 3 have been synthesized from D-(+)-tryptophan in enantiospecific fashion via