A new catalytic system for aerobic oxidative coupling of 2-naphthol derivatives by the use of CuCl-amine complex: A practical synthesis of binaphthol derivatives

Tetrahedron Letters

Volumn 35, Issue 43, 1994, Pages 7983-7984

  Noji, Masahiro ^a   Nakajima, Makoto ^a   Koga, Kenji ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BINAPHTHYL DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0027997060     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(94)80028-6     Document Type: Article

References (16)

1. Darstellung von Binaphthylendioxyd
2. Asymmetric phenol oxidation. Stereospecific and stereoselective oxidative coupling of a chiral tetrahydronaphthol
3. Oxidative coupling reactions of phenols with iron(III) chloride in the solid state
4. Oxidative coupling of phenols
5. Synthesis and chiral recognition of optically active crown ethers incorporating a biphenanthryl moiety as the chiral centre
6. Oxidative phenol coupling with cupric-amine complexes
7. Biomimetic asymmetric oxidative coupling of phenols
8. Stereoselective oxidative coupling and asymmetric hydride reduction related to (?)-(S)-10,10?-dihydroxy-9,9?-biphenanthryl
9. On the mechanism of the formation of s(−)-(1, 1'-binaphthalene)-2,2'-diol via copper(II)amine complexes
10. Highly selective oxidative cross-coupling of substituted 2-naphthols: A convenient approach to unsymmetrical 1,1′-binaphthalene-2,2′-diols
11. Synthesis of enantiomerically pure 2,2'-dihydroxy-1,1'-binaphthyl, 2,2'-diamino-1,1'-binaphthyl, and 2-amino-2'-hydroxy-1,1'-binaphthyl. Comparison of processes operating as diastereoselective crystallization and as second order asymmetric transformation
12. Synthesis of enantiomerically pure binaphthyl derivatives. Mechanism of the enantioselective, oxidative coupling of naphthols and designing a catalytic cycle