1538555-29-1

Basic information

• Product Name: (+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione
• Synonyms: (+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione
• CAS NO: 1538555-29-1
• Molecular Weight: 326.395
• Mol File: 1538555-29-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione(1538555-29-1)
• EPA Substance Registry System: (+)-11-(2-aminophenyl)-4a-ethyl-3,4,4a,5,6,7-hexahydropyrano[3,2-h]indolizine-2,9-dione(1538555-29-1)

Safety Data

• Hazardous Substances Data: 1538555-29-1(Hazardous Substances Data)

Upstream product

• 1236143-34-2 (-)-scholarisine G 
• 128529-80-6 6β,7β-dibromodiazaspiroleuconolam 
• 67-56-1 methanol 
• 93710-27-1 (?)-leuconolam 

Relevant articles and documents

Total Syntheses of (-)-Mersicarpine, (-)-Scholarisine G, (+)-Melodinine E, (-)-Leuconoxine, (-)-Leuconolam, (-)-Leuconodine A, (+)-Leuconodine F, and (-)-Leuconodine C: Self-Induced Diastereomeric Anisochronism (SIDA) Phenomenon for Scholarisine G and Leu

(Chemical Equation Presented) Enantioselective total syntheses of title natural products from a common cyclohexenone derivative (S)-18 were reported. Ozonolysis of (S)-18 afforded a stable diketo ester (R)-17 that was subsequently converted to two skeleta