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Volumn 65, Issue 10, 2000, Pages 3255-3258

Double annulation route to highly substituted and functionalized cis bicyclic and tricyclic δ-lactams and imides

Author keywords

[No Author keywords available]

Indexed keywords

IMIDE; LACTAM;

EID: 0034685735     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0000978     Document Type: Note
Times cited : (12)

References (24)
  • 5
    • 0006177179 scopus 로고
    • The earliest mention of this reaction seems to be in: Engelhardt, A. Ann. 1858, 108, 341.
    • (1858) Ann. , vol.108 , pp. 341
    • Engelhardt, A.1
  • 6
    • 0342274752 scopus 로고    scopus 로고
    • Only one conformer of each compound is shown in the table; however, the two chair conformers of each bicyclic compound are close in energy, and conformational flexibility is expected
    • Only one conformer of each compound is shown in the table; however, the two chair conformers of each bicyclic compound are close in energy, and conformational flexibility is expected.
  • 22
    • 0342274749 scopus 로고    scopus 로고
    • Prepared by Jones oxidation of commercially available 1-phenyl-3-propyn-1-ol
    • Prepared by Jones oxidation of commercially available 1-phenyl-3-propyn-1-ol.
  • 24
    • 0343144288 scopus 로고    scopus 로고
    • If the reaction is not allowed to proceed for enough time or the conditions are insufficiently acidic, the undehydrated aldol is isolated also
    • If the reaction is not allowed to proceed for enough time or the conditions are insufficiently acidic, the undehydrated aldol is isolated also.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.