Works matching IS 08990042 AND DT 1996 AND VI 8 AND IP 8
Results: 10
Chiral synthesis and pharmacological evaluation of the enantiomers of SM<sub>32</sub>, a new analgesic and cognition-enhancing agent.
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- Chirality, 1996, v. 8, n. 8, p. 579, doi. 10.1002/(SICI)1520-636X(1996)8:8<579::AID-CHIR7>3.0.CO;2-4
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Synthesis and analysis of the enantiomers of calmidazolium, and a <sup>1</sup>H NMR demonstration of a chiral interaction with calmodulin.
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- Chirality, 1996, v. 8, n. 8, p. 545, doi. 10.1002/(SICI)1520-636X(1996)8:8<545::AID-CHIR2>3.0.CO;2-8
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Impact of substituents on the enantioseparation of racemic 2-amidotetralins on polysaccharide stationary phases. I. chiralcel OD.
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- Chirality, 1996, v. 8, n. 8, p. 574, doi. 10.1002/(SICI)1520-636X(1996)8:8<574::AID-CHIR6>3.0.CO;2-9
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Synthesis and pharmacology of the enantiomers of UH301: Opposing interactions with 5-HT<sub>1A</sub> receptors.
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- Chirality, 1996, v. 8, n. 8, p. 531, doi. 10.1002/(SICI)1520-636X(1996)8:8<531::AID-CHIR1>3.0.CO;2-C
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Steric aspects of formoterol and terbutaline: Is there an adverse effect of the distomer on airway smooth muscle function?
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- Chirality, 1996, v. 8, n. 8, p. 567, doi. 10.1002/(SICI)1520-636X(1996)8:8<567::AID-CHIR5>3.0.CO;2-6
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Elucidation of vancomycin's enantioselective binding site using its copper complex.
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- Chirality, 1996, v. 8, n. 8, p. 590, doi. 10.1002/(SICI)1520-636X(1996)8:8<590::AID-CHIR9>3.0.CO;2-D
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Circular dichroism evidence of the left-handed conformation adopted by cyclopropylpyrroloindole antitumor antibiotics in solution.
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- Chirality, 1996, v. 8, n. 8, p. 585, doi. 10.1002/(SICI)1520-636X(1996)8:8<585::AID-CHIR8>3.0.CO;2-8
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Enantioselective separation of cyclic chiral ketones and their corresponding diastereomeric alcohols by HPLC on chiral and chiral/chiral coupled stationary phases.
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- Chirality, 1996, v. 8, n. 8, p. 551, doi. 10.1002/(SICI)1520-636X(1996)8:8<551::AID-CHIR3>3.0.CO;2-C
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Masthead.
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- Chirality, 1996, v. 8, n. 8, p. fmi, doi. 10.1002/chir.530080801
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Substituent effects on the enantioselective retention of anti-HIV 5-aryl-Δ<sup>2</sup>-1,2,4-oxadiazolines on R, R-DACH-DNB chiral stationary phase.
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- Chirality, 1996, v. 8, n. 8, p. 556, doi. 10.1002/(SICI)1520-636X(1996)8:8<556::AID-CHIR4>3.0.CO;2-7
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