Works matching IS 08990042 AND DT 2004 AND VI 16 AND IP 1

Results: 8

Stereoselective metabolism of methadone N-demethylation by cytochrome P4502B6 and 2C19(Abbreviations: CYP, cytochrome P450, EDDP, 2-Ethylidene-1,5-dimethyl-3, 3-diphenylpyrrolidine, LLQ, lower limit of quantitation.)This work was presented in part at the First International Workshop on Clinical Pharmacology of HIV Therapy, Noordwijk, the Netherlands, 2000, Abstract 2.2, and at the 2001 Annual Meeting of the American Society for Clinical Pharmacology and Therapeutics, Orlando, FL, Abstract PI39.)

Published in:

Chirality, 2004, v. 16, n. 1, p. 36

By:

John G. Gerber;
Robert J. Rhodes;
Joseph Gal

Publication type:

Article

Chiral aldehydes in hydrocarbons: diastereoselective nucleophilic addition, NMR, and CD spectroscopy reveal dynamic solvation effects(This article includes Supplementary Material available via the Internet at http://www.interscience.wiley.com/jpages/0899-0042/suppmat/16/v16.50.html.)

Published in:

Chirality, 2004, v. 16, n. 1, p. 50

By:

Gianfranco Cainelli;
Paola Galletti;
Silvia Pieraccini;
Arianna Quintavalla;
Daria Giacomini;
Gian Piero Spada

Publication type:

Article

Secondary phosphine oxides: tautomerism and chiral recognition monitored by multinuclear NMR spectroscopy of their Rh2[(R)-MTPA]4 adducts.

Published in:

Chirality, 2004, v. 16, n. 1, p. 57

By:

Damian Magiera;
Anna Szmigielska;
K. Michal Pietrusiewicz;
Helmut Duddeck

Publication type:

Article

Separation of cefoperazone enantiomers using β-cyclodextrin as chiral additive by capillary zone electrophoresis.

Published in:

Chirality, 2004, v. 16, n. 1, p. 45

By:

Rong Wang;
Zheng-Ping Jia;
Jun-Jie Fan;
Xiao-Li Hu;
Yong-Min Li;
Li-Ren Chen;
Jing-Wen Xie;
Qiang Zhang

Publication type:

Article

Enantioresolution of fluorinated diphenylmethanols and determination of their absolute configurations by X-Ray crystallographic and 1H NMR anisotropy methods.

Published in:

Chirality, 2004, v. 16, n. 1, p. 22

By:

Junpei Naito;
Masashi Kosaka;
Takeo Sugito;
Masataka Watanabe;
Nobuyuki Harada;
William H. Pirkle

Publication type:

Article

Novel chiral sulfur-containing ferrocenyl ligands for palladium-catalyzed asymmetric allylic substitution.

Published in:

Chirality, 2004, v. 16, n. 1, p. 10

By:

Shuichi Nakamura;
Takeo Fukuzumi;
Takeshi Toru

Publication type:

Article

Stereospecificity of flobufen metabolism in guinea pigs in vitro and in vivo: Phase I of biotransformation.

Published in:

Chirality, 2004, v. 16, n. 1, p. 1

By:

Radim Kral;
Lenka Skalova;
Barbora Szotakova;
Yogeeta N. Babu;
Vladimir Wsol

Publication type:

Article

Absolute configuration of the thyroid hormone analog KAT-2003 as determined by the 1H NMR anisotropy method with a novel chiral auxiliary, MαNP acid.

Published in:

Chirality, 2004, v. 16, n. 1, p. 13

By:

Toshihiro Nishimura;
Hiromi Taji;
Nobuyuki Harada

Publication type:

Article

Works matching IS 08990042 AND DT 2004 AND VI 16 AND IP 1

Chiral aldehydes in hydrocarbons: diastereoselective nucleophilic addition, NMR, and CD spectroscopy reveal dynamic solvation effects(This article includes Supplementary Material available via the Internet at http://www.interscience.wiley.com/jpages/0899-0042/suppmat/16/v16.50.html.)

Secondary phosphine oxides: tautomerism and chiral recognition monitored by multinuclear NMR spectroscopy of their Rh<sub>2</sub>[(R)-MTPA]<sub>4</sub> adducts.

Separation of cefoperazone enantiomers using β-cyclodextrin as chiral additive by capillary zone electrophoresis.

Enantioresolution of fluorinated diphenylmethanols and determination of their absolute configurations by X-Ray crystallographic and <sup>1</sup>H NMR anisotropy methods.

Novel chiral sulfur-containing ferrocenyl ligands for palladium-catalyzed asymmetric allylic substitution.

Stereospecificity of flobufen metabolism in guinea pigs in vitro and in vivo: Phase I of biotransformation.

Absolute configuration of the thyroid hormone analog KAT-2003 as determined by the <sup>1</sup>H NMR anisotropy method with a novel chiral auxiliary, MαNP acid.