1970
DOI: 10.1016/s0031-9422(00)85157-2
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A general method for the isolation of naturally occurring water-soluble bases

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Cited by 27 publications
(7 citation statements)
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“…The aqueous layer, after extraction with ether and ethyl acetate, was treated with saturated solution of ammonium reineckate at pH ca. 8 [16]. The reineckate salt was collected by filtration.…”
Section: Treatment Of Aqueous Portionmentioning
confidence: 99%
See 1 more Smart Citation
“…The aqueous layer, after extraction with ether and ethyl acetate, was treated with saturated solution of ammonium reineckate at pH ca. 8 [16]. The reineckate salt was collected by filtration.…”
Section: Treatment Of Aqueous Portionmentioning
confidence: 99%
“…The aqueous filtrate from the above was acidified (pH ca. 2) and again treated with a saturated solution of ammonium reineckate [16]. The base reineckates were converted [8] to the corresponding hydrochlorides by stirring the EtOH solution with Amberlite IRA-400 (Cr) resin for 8 hrs.…”
Section: Hypaphorine Methyl Estermentioning
confidence: 99%
“…T h e alkaloid mixture from the alcoholic extract was broadly divided into three categories, according to a previously described procedure (GHOSAL et al, 1970), viz., CHCl,rsolub!e acetates, CHC1,-soluble moderately strong bases, and water-soluble bases. light petrol.…”
Section: Methodsmentioning
confidence: 99%
“…Gradient-pH extraction (GHOSAL et al, 1970), fractionation into phenolic and non-phenolic bases over Amberlite IRA-400 resin columns (LUNDSTROM and AGURELL, 1967), precipitation of reineckate salts of water-solubie alkaloids under basic and acidic conditions, and regeneration of the bases over De-Acidite FF (GHOSAL et al, 1970), resulted in the isolation of seven 0-phenethylamines (I-VlI) and one tetrahydroisoquinoline ( derivatives with those reported in the literature, mixed melting points, co-TLC with authentic reference materials, by the usual chemical transformations into known compounds, and from the spectral (UV, IR, PMR,lMS) properties. Gradient-pH extraction (GHOSAL et al, 1970), fractionation into phenolic and non-phenolic bases over Amberlite IRA-400 resin columns (LUNDSTROM and AGURELL, 1967), precipitation of reineckate salts of water-solubie alkaloids under basic and acidic conditions, and regeneration of the bases over De-Acidite FF (GHOSAL et al, 1970), resulted in the isolation of seven 0-phenethylamines (I-VlI) and one tetrahydroisoquinoline ( derivatives with those reported in the literature, mixed melting points, co-TLC with authentic reference materials, by the usual chemical transformations into known compounds, and from the spectral (UV, IR, PMR,lMS) properties.…”
Section: Chemistrymentioning
confidence: 99%
“…β-sitosterol, acylsteryglycoside sitoindoside [5], ephedrine, [25], S-(+)-Nbmethyltryptophan methylester, hypaphorine [3], vasicinone [26], vascicine, and vasicinol [6]. The roots contain 0.06% of alkaloid.…”
Section: Rootmentioning
confidence: 99%