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Volumn 71, Issue 10, 2006, Pages 3963-3966

Synthesis and receptor binding evaluation of clavizepine analogues with no ring D substituents

Author keywords

[No Author keywords available]

Indexed keywords

BINDING EVALUATION; CLAVIZEPINE; ELECTROPHILIC CYCLIZATION; SULFONAMIDE ACETALS;

EID: 33646534197     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052320c     Document Type: Article
Times cited : (16)

References (25)
  • 11
    • 0021811121 scopus 로고
    • This effect of para- and ortho-substituted aryl rings has been invoked to explain the observed racemization of homochiral benzylic alcohols during the Mitsunobu reaction: (a) Iida, H.; Yamazaki, N.; Kibayashi, C. Tetrahedron Lett. 1985, 26, 3255-3258.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 3255-3258
    • Iida, H.1    Yamazaki, N.2    Kibayashi, C.3
  • 21
    • 33646501265 scopus 로고    scopus 로고
    • note
    • 1H NMR of the crude cyclization product did not show the presence of the cis stereoisomer.
  • 23
    • 33646495360 scopus 로고    scopus 로고
    • Calculations were performed using software provided by R. Stenutz at http://www.casper.organ.su.se/.
    • Stenutz, R.1
  • 24
    • 33646514703 scopus 로고    scopus 로고
    • note
    • The alternative distorted half-chair conformation with the trifluoroacetate group in a pseudoequatorial position is about 7 kcal/mol higher in energy.
  • 25
    • 33646512467 scopus 로고    scopus 로고
    • note
    • Molecular mechanics calculations were performed using the MM2 package of Chem-3D (CambridgeSoft Corporation, Cambridge, MA).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.