Synthesis of 3-alkoxy-4-hydroxyphenylacetic acids from methyl 3-alkoxybenzoates

Synthetic Communications

Volumn 31, Issue 3, 2001, Pages 455-462

  Jung, Young Sik ^a   Kang, Tae Souk ^a   Lee, Jong Cheol ^a   Seong, Churl Min ^a   Ham, Won Hun ^b   Park, No Sang ^a  

^a Korea Research Institute of Chemical Technology   (South Korea)

^b Sungkyunkwan University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXYPHENYLACETIC ACID DERIVATIVE; ANALGESIC AGENT; BENZOIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VANILLOID DERIVATIVE;

ALKYLATION; ANALGESIC ACTIVITY; ARTICLE; DRUG SYNTHESIS; HYDROLYSIS; OXIDATION; SPECTROSCOPY;

EID: 0035084696     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-100000539     Document Type: Article

References (10)

1. Capsaicin: Cellular targets, mechanisms of action, and selectivity for thin sensory neurons
2. The neuropharmacology of capsaicin: Review of some recent observations
3. Vanilloid receptors: New insights enhance potential as a therapeutic target
4. Analogues of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 1. The aromatic "A-Region"
5. Analogues of capsaicin with agonist activity as novel analgesic agents; structure-activity studies. 4. Potent, orally active analgesics
6. Homovanillic amide derivatives as capsaicin analogs and their analgesic activity
7. 2 in vanillin or homovanillin ring of capsaicinoids
8. Recent developments in the birch reduction of aromatic compounds: Applications to the synthesis of natural products
9. A synthetically useful conversion of benzoic acid derivatives to 4-alkylphenols and 4-alkyl-3-carbalkoxyphenols
10. Photochemical and acid-catalyzed dienone-phenol rearrangements. The effect of substituents on the regioselectivity of 1,4-sigmatropic rearrangements of the type A intermediate