메뉴 건너뛰기




Volumn 4, Issue 24, 2002, Pages 4353-4356

2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE;

EID: 0041736499     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol027039o     Document Type: Article
Times cited : (19)

References (31)
  • 1
    • 0000688042 scopus 로고
    • For a review of 2-azabicyclo[2.2.1]heptanes, see: Blondet, D.; Morin, C. Heterocycles 1982, 19, 2155-2182.
    • (1982) Heterocycles , vol.19 , pp. 2155-2182
    • Blondet, D.1    Morin, C.2
  • 7
    • 0000108509 scopus 로고
    • Kochi, J. K., Ed.; Wiley: New York
    • (c) Wilt, J. W. In Free Radicals; Kochi, J. K., Ed.; Wiley: New York, 1973; Vol. 1, pp 333-502.
    • (1973) Free Radicals , vol.1 , pp. 333-502
    • Wilt, J.W.1
  • 15
    • 0035955789 scopus 로고    scopus 로고
    • (d) For a recent review of radical aryl migrations, see: Studer, A.; Bossart, M. Tetrahedron 2001, 57, 9649-9667.
    • (2001) Tetrahedron , vol.57 , pp. 9649-9667
    • Studer, A.1    Bossart, M.2
  • 25
    • 0041324027 scopus 로고    scopus 로고
    • 2Me) to give the free amine 7a (R = H), which had spectroscopic data matching those given in ret 9 for 7a (R = H)
    • 2Me) to give the free amine 7a (R = H), which had spectroscopic data matching those given in ret 9 for 7a (R = H).
  • 26
    • 0041824623 scopus 로고    scopus 로고
    • Studies on the kinetics of the process are currently underway in our laboratories
    • Studies on the kinetics of the process are currently underway in our laboratories.
  • 28
    • 0001183751 scopus 로고
    • Ethylpyrrole was prepared by hydrolysis (KOH) of the known 3-ethyl-1-phenylsulfonylpyrrole, see: Ketcha, D. M.; Carpenter K. P.; Atkinson, S. T.; Rajagopolan, H. R. Synth. Commun. 1990, 1647-1655. 2,4-Dimethylpyrrole is commercially available (Aldrich).
    • (1990) Synth. Commun. , pp. 1647-1655
    • Ketcha, D.M.1    Carpenter, K.P.2    Atkinson, S.T.3    Rajagopolan, H.R.4
  • 29
    • 0042826635 scopus 로고    scopus 로고
    • 15 of the benzyne cycloadducts
    • 15 of the benzyne cycloadducts.
  • 30
    • 0000728919 scopus 로고
    • See Supporting Information for the preparation of 3d and 3e. Adduct 3f was prepared according to the procedure of Bornstein, see: Remy, D. E.; Bissett, F. H.; Bornstein, J. J. Org. Chem. 1978, 43, 4469-4472.
    • (1978) J. Org. Chem. , vol.43 , pp. 4469-4472
    • Remy, D.E.1    Bissett, F.H.2    Bornstein, J.3
  • 31
    • 0042826634 scopus 로고    scopus 로고
    • % of directly reduced product was isolated from the reaction of 5d
    • % of directly reduced product was isolated from the reaction of 5d.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.