Diastereoselective Synthesis of β-Amino Alcohols via Bu3SnH-Mediated Reductive Cyclization of Carbonyl−Oxime Ethers
- 1 January 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (1) , 201-202
- https://doi.org/10.1021/jo971574y
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Bu3SnH-Catalyzed Barton−McCombie Deoxygenation of AlcoholsJournal of the American Chemical Society, 1997
- A Novel and Chiral Synthesis of Both Enantiometers of trans-3-Amino-4-hydroxyhexahydroazepine, a Key Intermediate for the Synthesis of Balanol.CHEMICAL & PHARMACEUTICAL BULLETIN, 1996
- Intramolecular reductive coupling of carbonyl-tethered oxime ethers promoted by samarium diiodide: A powerful method for the stereoselective synthesis of aminocyclopentitolsThe Journal of Organic Chemistry, 1995
- A novel and concise synthesis of aminocyclopentitols and 1-deoxynojirimycin via radical cyclization of oxime ethersTetrahedron Letters, 1995
- Radical cyclization of oxime ethersJournal of the American Chemical Society, 1988