25095-06-1Relevant academic research and scientific papers
STEREOSPECIFIC FUNCTIONALIZATION OF THE HETEROCYCLIC RING SYSTEMS OF FLAVAN-3-OL AND -BIFLAVAN-3-OL DERIVATIVES WITH 2,3-DICHLORO-5,6-DICYANO-1,4-BENZOQUINONE (DDQ)
Steenkamp, Jacobus A.,Ferreira, Daneel,Roux, David G.
, p. 3045 - 3048 (2007/10/02)
Efficient stereospecific 4-methoxylation of both 2,3-trans- and 2,3-cis-flavan-3-ol methyl ethers with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) in CHCL3-MeOH solution is of both synthetic and degradative significance in oligomeric flavanoid chemist
Synthesis of Condensed Tannins. Part 1. Stereoselective and Stereospecific Syntheses of Optically Pure 4-Arylflavan-3-ols, and Assessment of their Absolute Stereochemistry at C-4 by means of Circular Dichroism
Botha, Jacobus J.,Young, Desmond A.,Ferreira, Daneel,Roux, David G.
, p. 1213 - 1219 (2007/10/02)
Stereoselective and also stereospecific condensation at C-4 of flavan-3,4-diols of known absolute configuration with phloroglucinol and resorcinol in acid medium proceeds at ambient temperatures with partial retention of configuration for 2,3-trans-isomers and with inversion for 2,3-cis-analogues.Circular dichroism spectra of the resultant 4-arylflavan-3-ols all exhibit multiple Cotton effects.The sign of high intensity Cotton effects to low wavelength, contributed by aryl chromophores at C-4, may almost invariably be correlated with the absolute configuration at this chiral centre of 2,3-trans-3,4-trans, 2,3-trans-3,4-cis, and 2,3-cis-3,4-trans-isomers.
