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Bulletin of the Chemical Society of Japan

Volumn 75, Issue 8, 2002, Pages 1777-1783

The conformation of 2-phenylpropionaldehyde and alkyl 1-phenylethyl ketones as evidenced by Ab initio calculations. Relevance of the CH/π and CH/O interactions in stereochemistry

(6) Takahashi, Osamu a Yasunaga, Kenji a Gondoh, Yoshinobu a Kohno, Yuji a Saito, Ko a Nishio, Motohiro b

a HIROSHIMA UNIVERSITY (Japan)

b CHPI Institute (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONAL ENERGIES;

CONFORMATIONS; ELECTROSTATICS; ENTHALPY; KETONES; NUCLEAR MAGNETIC RESONANCE;

STEREOCHEMISTRY;

1 PHENYLETHYL KETONE; 2 PHENYLPROPIONALDEHYDE; ALDEHYDE DERIVATIVE; ALKYL GROUP; FORMIC ACID METHYL ESTER; HYDROGEN; KETONE DERIVATIVE; N METHYLFORMAMIDE; PROPIONALDEHYDE; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CHEMICAL STRUCTURE; CONFORMATION; ELECTRICITY; ENERGY; ENTHALPY; MOLECULAR INTERACTION; MOLECULAR STABILITY; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 0036353951 PISSN: 00092673 EISSN: None Source Type: Journal
DOI: 10.1246/bcsj.75.1777 Document Type: Article

Times cited : (28)

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