60313-84-0Relevant academic research and scientific papers
Enantioselective acylation of (±)-cis-flavan-4-ols catalyzed by lipase from Candida cylindracea (CCL) and the synthesis of enantiopure flavan-4-ones
Ramadas, Sathunuru,Krupadanam, G.L. David
, p. 3381 - 3391 (2007/10/03)
Lipase Candida cylindracea (CCL) catalyzed acylation of (±)-cis-flavan-4-ols using vinyl acetate as the acyldonor in DME-toluene (1:2) gave (-)-(2R,4R)-4-acetoxyflavans 9a-m and (+)-(2S,4S)-flavan-4-ols 10a-m in high enantiomeric excess. (+)-(2S,4S)-Flava
REDUCTION OF 2'-HYDROXY CHALCONES UNDER PHASE TRANSFER CATALYSIS - A NEW METHOD FOR THE SYNTHESIS OF FLAVAN-4-OLS
Jyotsna, D.,Rao, A. V. Subba
, p. 1009 - 1014 (2007/10/02)
Reduction of 2'-hydroxy chalcones uner phase transfer catalysis conditions is discussed.The products are identified as 2,4-cis-flavan-4-ols.
Synthesis and Reactions of 4-Aryloxyflavans
Bateman, Graham,Brown, Ben R.,Campbell, John B.,Cotton, Charles A.,Johnson, Philip,et al.
, p. 2903 - 2912 (2007/10/02)
4α-Aryloxyflavans unsubstituted in ring A have been synthesised by the reaction of phenols with flavan-4β-ols in the presence of boron trifluoride in ether.If reaction times are prolonged beyond disappearance of the starting 4β-ols, thermodynamic control leads to 4-arylflavans and the yields of 4-aryloxyflavans are negligible. 4-Arylflavans are the sole products when the catalyst is toluene-p-sulphonic acid.Thermal decomposition of flavan-4-yl phenol carbonate in the presence of phenols affords a synthesis of 4α-aryloxyflavans free from 4-arylflavans.Syntheses of 7-methoxy-4α-aryloxyflavans have not been successful, nor can 4-aryloxyflavan-3-ols be obtained from 3,4-diols by these methods.The 4-aryloxyflavans react rapidly with acids to yield 4-carbocations which can be trapped by a variety of nucleophiles yielding 4α-ols with water, 4α-alkoxyflavans with alcohols, 4α-arylflavans with phenols, and 4α-sulphides with thiols. 2,3-cis-Flav-3-ene epoxide reacts with phenols to give 2,3-cis-3,4-cis-4-aryloxyflavan-3-ols and with sodium salts of phenols to give 2,3-cis-3,4-trans-4-aryloxyflavan-3-ols.The 2,3-trans-epoxide similarly gives the 2,3-trans-4-aryloxyflavan-3-ols.A biflavonoid containing a 4-aryloxy link has been synthesised from the 2,3-trans-epoxide and 7-hydroxyflavan-4-one.A series of 2,3-trans-4'-methoxy-4-aryloxyflavan-3-ols has been synthesised from crude 2,3-trans-4'-methoxyflav-3-ene epoxide.The substitution of a methoxy group into position 7 of the flavonoid A-ring prevented the preparation of the epoxides, but the action of N-bromosuccinimide and sodium acetate in acetic anhydride and acetic acid on 7,4'-dimethoxyflav-3-ene gave 2,3-cis- and 2,3-trans-4-acetoxy-3-bromo-7,4'-dimethoxyflavans, the latter of which was converted by the action of sodium salts of phenols into the expected 4-aryloxyflavan-3-ols. 5,7,3',4'-Tetramethoxyflav-3-ene gave nuclear brominated products even with N-bromosuccinimide; thus, the synthesis of 5,6,3'4'-tetramethoxy-4-aryloxyflavan-3-ols has not been possible by this method.
