A Versatile Method for the Resolution and Absolute Configuration Assignment of Substituted 1,1‘-Bi-2-naphthols
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (24), 8712-8714
- https://doi.org/10.1021/jo9610927
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Synthesis, chiroptical and redox properties of axially chiral binaphthol-based oligomersTetrahedron: Asymmetry, 1996
- Synthesis and chiroptical properties of axially chiral, binaphthol-based oligomersTetrahedron Letters, 1996
- Catalytic asymmetric synthesis of binaphthol derivatives by aerobic oxidative coupling of 3-hydroxy-2-naphthoates with chiral diamine-copper complexTetrahedron Letters, 1995
- A new catalytic system for aerobic oxidative coupling of 2-naphthol derivatives by the use of CuCl-amine complex: a practical synthesis of binaphthol derivativesTetrahedron Letters, 1994
- Enantioselective, electrocatalytic oxidative coupling of naphthol, naphthyl ether and phenanthrol on a TEMPO-modified graphite felt electrode in the presence of (–)-sparteine (TEMPO = 2,2,6,6-tetramethylpiperidin-1-yloxyl)Journal of the Chemical Society, Chemical Communications, 1994
- A new and efficient method for the resolution of 2,2'-dihydroxy-1,1'-binaphthylThe Journal of Organic Chemistry, 1991
- Resolution of binaphthols and spirobiindanols using cholesterol esteraseJournal of the American Chemical Society, 1989
- Efficient Synthesis of Sterically Hindered Chiral Binaphthol DerivativesBulletin of the Chemical Society of Japan, 1988
- Efficient optical resolution of 2,2'-dihydroxy-1,1'-binaphthyl and related compounds by complex formation with novel chiral host compounds derived from tartaric acidThe Journal of Organic Chemistry, 1988
- Stereoselective oxidative coupling and asymmetric hydride reduction related to (–)-(S)-10,10′-dihydroxy-9,9′-biphenanthrylJournal of the Chemical Society, Chemical Communications, 1984