14C-labeled chlorogenic acid (specijic activity 30.6 nCilmg) was synthesized by reaction of diphenylmethyl-I-0-ethoxy-carbonyl- 4,5-0-isopropylidenequinate ( V ) with 0,O-dimethylcarbonyl caffeoyl chloride-u-14C (VIII) followed by selective hydrolysis of the protecting groups.
Improved conventional synthesis for 14C-labeled polyglutamates of folic acid
✍ Scribed by Catherine R. Ferenz; David Y. Graham
- Book ID
- 102901113
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 562 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
form and a r e unable t o support L a c t o b a c i l l u s casei growth u n t i l the 8-linked glutamyls are digested by conjugase enzyues. Most s t u d i e s involving f o l a t e absorption have u t i l i z e d monoglutamyl forms of f o l a t e , p r i m a r i l y f o l i c a c i d .
S y n t h e t i c pteroylpolyglutamates prepared by s o l i d phase o r conllentional
s y n t h e s i s provided conjugated materials with which t o s t u d y the absorption and uetabolism of n a t u r a l d e r i v a t i w s ; h o w w r , t h e s y n t h e t i c hepataglutamates support microbiological growth p r i o r t o enzymatic hydrolysis whereas t h e n a t u r a l conjugates do n o t .
Incomplete p u r i f i c a t i o n of i n t e r m d i a t e peptides during the s y n t h e s i s would be the most l i k e l y explanation of t h i s growth phenomnon. A modified s o l u t i o n s y n t h e s i s has been developed which improws upon intermediate peptide condensations, i n c r e a s e s product y i e l d s , and provides a heptapeptide which does n o t support microbiological growth u n t i l a f t e r enzymatic hydrolysis.
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