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Volumn 8, Issue 5, 1996, Pages 364-371

Enantiomerization of an atropisomeric drug

Author keywords

10 (3 chlorophenyl) 6,8,9,10 tetrahydrobenzo b 1,8 naphthyridin 5(7H) one; antipsoriatic agent; dynamic HPLCs; interconversion half lives; SIMUL; stereogenic axis

Indexed keywords

ANTIPSORIASIS AGENT; NAPHTHYRIDINE DERIVATIVE; SCH 40120; UNCLASSIFIED DRUG;

EID: 0029906741     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1996)8:5<364::AID-CHIR2>3.0.CO;2-E     Document Type: Article
Times cited : (45)

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    • 41 Lacking any estimate of the difference in transition state energies, we have not adjusted any of our values to take these changes into account. Although halving the rate constants would double the half-lives, the prolongation would not alter our conclusions regarding the nil consequences of the 40120 chirality. On the timescale of pharmaceutical development, a half-life increase to 3.2 min at 37°C would be insignificant. Adding the RTln2 term to the Gibbs free energies of activation would increase them only by about 2%.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.