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Volumn 41, Issue 40, 2000, Pages 7769-7772

Diastereoselective aziridination of cyclic dienes with 3-acetoxyaminoquinazolin-4(3H)-ones: Competitive formation of insertion products from cyclohexadienes

Author keywords

[No Author keywords available]

Indexed keywords

3 ACETOXYAMINOQUINAZOLINONE DERIVATIVE; ALKADIENE; AZIRIDINE DERIVATIVE; CYCLOHEPTADIENE; CYCLOHEXA 1,3 DIENE DERIVATIVE; CYCLOPENTADIENE DERIVATIVE; TITANIUM; UNCLASSIFIED DRUG;

EID: 0034734656     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)01328-9     Document Type: Article
Times cited : (6)

References (14)
  • 3
    • 85037934021 scopus 로고    scopus 로고
    • 1NHOAc 1 is prepared from (S)-tert-leucine
  • 4
    • 85037941935 scopus 로고    scopus 로고
    • note
  • 5
    • 85037932368 scopus 로고    scopus 로고
    • The configuration shown in 4 is assigned by analogy with that of 3a
  • 7
    • 85037942600 scopus 로고    scopus 로고
    • Occasionally the dr was lower at 4:1 for reasons not as yet clear
  • 8
    • 85037936647 scopus 로고    scopus 로고
    • A by-product in this reaction was the allyl aryl thioether from S(N)2 ring-opening (10%)
  • 10
    • 0000014210 scopus 로고
    • Nitrenes and Azides, Reactivity and Utility; Scriven, E. F. V., Ed.; Academic: New York
    • (1984) , pp. 205-246
    • Lwowski, W.1
  • 12
    • 85037949499 scopus 로고    scopus 로고
    • 2NHOAc 5 (12% yield)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.