14050-94-3

Basic information

• Product Name: (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-hydroxycinchonane
• Synonyms: (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-hydroxycinchonane
• CAS NO: 14050-94-3
• Molecular Weight: 310.396
• Mol File: 14050-94-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-hydroxycinchonane(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-hydroxycinchonane(14050-94-3)
• EPA Substance Registry System: (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-hydroxycinchonane(14050-94-3)

Safety Data

• Hazardous Substances Data: 14050-94-3(Hazardous Substances Data)

Upstream product

• 56-54-2 quinidine 
• 5056-73-5 (3R,8R,9S)-10,11-dihydro-3,9-epoxy-6'-methoxycinchonane 

Downstream Products

• 1321139-96-1 C₂₇H₃₀N₂O₃ 

Relevant articles and documents

β-Isocupreidine-hexafluoroisopropyl acrylate method for asymmetric Baylis-Hillman reactions

Key features of the β-isocupreidine (β-ICD)-catalyzed asymmetric Baylis-Hillman reaction of aldehydes with 1,1,1,3,3,3-hexafluoroisopropyl acrylate (HFIPA) are presented. In addition, an improved method using azeotropically dried β-ICD is described.

Asymmetric synthesis of natural product inspired tricyclic benzopyrones by an organocatalyzed annulation reaction

(Chemical Equation Presented) Going back to nature: Electron-deficient oxadienes and electron-poor acetylene carboxylates react in the presence of an organocatalyst to give natural product inspired tricyclic benzopyrones efficiently (up to 99% yield) and