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Volumn 36, Issue 4, 1995, Pages 625-628

Conformationally constrained dipeptides: Synthesis of 7,5- and 6,5-fused bicyclic lactams by stereoselective radical cyclizations

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAM DERIVATIVE;

EID: 0028881546     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(94)02319-7     Document Type: Article
Times cited : (48)

References (25)
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    • Reviews on protease inhibitors:
    • (1991) J. Med. Chem. , vol.34 , pp. 2305-2314
    • Huff1
  • 18
    • 20444483055 scopus 로고
    • Calculated coupling constants were Boltzman averaged values at 295°K, obtained by the application of the Altona equation:
    • (1980) Tetrahedron , vol.36 , pp. 2783-2792
    • Haasnoot1    De Leeuw2    Altona3
  • 20
    • 85034533375 scopus 로고
    • Acyclic Diastereofacial Selection in Intermolecular Radical Reactions StericvsElectronic Controls
    • (1994) Synlett , pp. 1-26
    • Smadja1
  • 25
    • 0006560014 scopus 로고
    • The regiochemical outcomes of the above radical cyclizations are in agreement with the coefficients of the LUMO calculated with MO theory at UHF/STO-3G level on the radical generated from 6, 7 and 8. The SOMO-LUMO interaction appears to be more important than the SOMO-HOMO one, as proposed by Fukui
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 9205-9210
    • Fujimoto1    Yamabe2    Minato3    Fukui4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.