Identification and synthesis of O-methylcatechol metabolites of phenobarbital and some N-alkyl derivatives

DOI: 10.1002/jps.2600760617

Source and publish data:

Journal of Pharmaceutical Sciences p. 496 - 501 (1987)

Update date:2022-08-03

Topics:

Authors:

Treston Treston

Philippides

Jacobsen

Eadie Eadie

Hooper Hooper

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/jps.2600760617

Full text of DOI:10.1002/jps.2600760617

Products guided by the article

Product name:methyl 4-carbethoxy-3-methoxyphenylethanoate

Cas No:110879-31-7

R&D Labs maybe for 110879-31-7

Shifang Taifeng New Flame Retardant Co., Ltd

Contact:02884721008

Address:tingjiang industrial park, hefeng town
Sinonine Industry Co.,Ltd

Contact:86+21-56421993

Address:3F,BUILDING 10,NO.2889 JINKE ROAD, SHANGHAI.
NEW FORTUNE INDUSTRIAL CO.,LTD.

website:http://newfortune.lookchem.com/

Contact:+86-25-8645-9456

Address:C4-105 GREEN ISLAND FLOWER TOWN
YingYing Pharmaceutical Co.,Ltd

Contact:86-18854126208

Address:55#, yingxiongshan road
N&R INDUSTRIES,INC

Contact:Tel:+86-29-88764861 Fax:+86-29-88764861

Address:Rm#2107, Block A, Epin Meidao Building, Gaoxin Rd, Hi-Tech Zone, Xi’an, China

Relevant to this article

Thermal epimerization of diastereomeric Grignard reagents

Doi:10.1039/b819178f
(2009)
MECHANISM OF THE FISCHER INDOLE SYNTHESIS. QUANTUM-CHEMICAL INTERPRETATION OF THE REARRANGEMENT OF SUBSTITUTED CYCLOHEXANONE ARYLHYDRAZONES TO TETRAHYDROCARBAZOLES

Doi:10.1007/BF00522729
(1986)
Cu(I)/Ag(I)-mediated decarboxylative trifluoromethylation of arylpropiolic acids with Me₃SiCF₃at room temperature

Doi:10.1016/j.tet.2016.05.012
(2016)
Graphene oxide nanosheets promoted regioselective and green synthesis of new dicoumarols

Doi:10.1039/c4ra00508b
(2014)
SYNTHESIS AND CHEMICAL TRANSFORMATIONS OF CYCLOBUTA NAPHTHALENE AND -ANTHRACENE DERIVATIVES

Doi:10.1016/S0040-4039(00)95821-0
(1987)
A facile one-pot synthesis of the very useful building blocks N-boc-S- alkylatedcysteines

Doi:10.1016/S0040-4020(99)00528-1
(1999)

Article Doi