755759-22-9

Basic information

• Product Name: methyl (3R,7R,8S,8aR)-8-ethyl-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate
• Synonyms: methyl (3R,7R,8S,8aR)-8-ethyl-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate
• CAS NO: 755759-22-9
• Molecular Weight: 432.519
• Mol File: 755759-22-9.mol

Chemical Properties

• CAS DataBase Reference: methyl (3R,7R,8S,8aR)-8-ethyl-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (3R,7R,8S,8aR)-8-ethyl-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate(755759-22-9)
• EPA Substance Registry System: methyl (3R,7R,8S,8aR)-8-ethyl-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate(755759-22-9)

Safety Data

• Hazardous Substances Data: 755759-22-9(Hazardous Substances Data)

Upstream product

• 21422-40-2 methyl 1H-indole-2-acetate 
• 457622-91-2 (3R,8S,8aR)-8-ethyl-5-oxo-3-phenyl-2,3,8,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine 

Relevant articles and documents

Enantioselective formal synthesis of uleine alkaloids from phenylglycinol-derived bicyclic lactams

A two-step route for the enantioselective construction of the tetracyclic ring system of uleine alkaloids, involving the stereoselective conjugate addition of an appropriate indole-containing nucleophile to a chiral bicyclic δ-lactam and the subsequent cy

Conjugate additions to phenylglycinol-derived unsaturated δ-lactams. Enantioselective synthesis of uleine alkaloids

The stereochemical outcome of the conjugate addition of a variety of stabilized nucleophiles (2-indoleacetic enolates and sulfur-stabilized anions) to the phenylglycinol-derived unsaturated lactams trans-2, cis-2, and its 8-ethyl-substituted analogue 10 i