ketopinic-acid and 2-naphthol

ketopinic-acid has been researched along with 2-naphthol* in 1 studies

Other Studies

1 other study(ies) available for ketopinic-acid and 2-naphthol

Article	Year
Catalytic asymmetric oxidative couplings of 2-naphthols by tridentate N-ketopinidene-based vanadyl dicarboxylates. Organic letters, 2002, Jul-25, Volume: 4, Issue:15 [reaction: see text] A series of oxovanadium(IV) complexes derived from tridentate N-ketopinidene-alpha-amino acids were synthesized. They serve as efficient catalysts for the enantioselective oxidative couplings of various 3-, 6-, or 7-substituted 2-naphthols. The best scenario involves the use of a vanadyl complex arising from L-tert-leucine in CCl4. The asymmetric couplings of 2-naphthols can be conducted smoothly at 40-45 degrees C under a stream of gaseous oxygen, leading to 2,2'-dihydroxy-1,1'-binaphthyls in good yields (61-99%) and with enantioselectivities of up to 87%. Topics: Amino Acids; Bridged-Ring Compounds; Catalysis; Dimerization; Ketones; Naphthols; Oxygen; Vanadates	2002

Article

Year

Catalytic asymmetric oxidative couplings of 2-naphthols by tridentate N-ketopinidene-based vanadyl dicarboxylates.

Organic letters, 2002, Jul-25, Volume: 4, Issue:15

[reaction: see text] A series of oxovanadium(IV) complexes derived from tridentate N-ketopinidene-alpha-amino acids were synthesized. They serve as efficient catalysts for the enantioselective oxidative couplings of various 3-, 6-, or 7-substituted 2-naphthols. The best scenario involves the use of a vanadyl complex arising from L-tert-leucine in CCl4. The asymmetric couplings of 2-naphthols can be conducted smoothly at 40-45 degrees C under a stream of gaseous oxygen, leading to 2,2'-dihydroxy-1,1'-binaphthyls in good yields (61-99%) and with enantioselectivities of up to 87%.

Topics: Amino Acids; Bridged-Ring Compounds; Catalysis; Dimerization; Ketones; Naphthols; Oxygen; Vanadates

2002