Absolute configuration assignment of norcamphor-derived furyl hydroperoxide using density functional theory calculations of optical rotation and vibrational circular dichroism

Journal of Organic Chemistry

Volumn 75, Issue 7, 2010, Pages 2179-2188

  Lattanzi, Alessandra ^a   Scettri, Arrigo ^a   Zanasi, Riccardo ^a   Devlin, Frank J ^b   Stephens, Philip J ^b  

^a UNIVERSITY OF SALERNO   (Italy)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; CONFORMATIONAL FLEXIBILITY; D LINES; DENSITY FUNCTIONAL THEORY CALCULATIONS; DIASTEREOISOMERS; HYDROPEROXIDES; IR ABSORPTION SPECTRA; NORCAMPHOR; SPECIFIC ROTATIONS; STEREO-SELECTIVE; STEREOGENIC CARBONS; STRUCTURAL IDENTIFICATION; VIBRATIONAL CIRCULAR DICHROISM;

DICHROISM; ISOMERS; OPTICAL ROTATION; ROTATION; SODIUM;

DENSITY FUNCTIONAL THEORY;

CAMPHOR DERIVATIVE; CARBON; FURYL HYDROPEROXIDE; HYDROPEROXIDE DERIVATIVE; NORCAMPHOR DERIVATIVE; OXIDIZING AGENT; SODIUM; UNCLASSIFIED DRUG;

ARTICLE; CIRCULAR DICHROISM; CONFORMATION; CONTROLLED STUDY; DENSITY FUNCTIONAL THEORY; DIASTEREOISOMER; INFRARED RADIATION; LIGHT ABSORPTION; OPTICAL ROTATION; STEREOCHEMISTRY; STRUCTURE ANALYSIS; VIBRATION; VIBRATIONAL CIRCULAR DICHROISM;

EID: 77950333574     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo902472b     Document Type: Article

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