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Volumn 63, Issue 17, 1998, Pages 5728-5729

Directing Effect of a Neighboring Aromatic Group in the Cyclopropanation of Allylic Alcohols

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EID: 0000660109     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9806815     Document Type: Article
Times cited : (14)

References (26)
  • 11
    • 85034465134 scopus 로고    scopus 로고
    • note
    • n; (iii) Zn(Cu), i-PrOH, THF reflux.
  • 12
    • 33845278128 scopus 로고
    • (b) For the preparation of aldehydes involved in the synthesis of 5 and 6, see: Maruoka, K.; Itoh, T.; Sakurai, M.; Nonoshita, K.; Yamamoto, H. J. Am. Chem. Soc. 1988, 110, 3588-3597. (c) Smith, A. B., III; Qiu, Y.; Jones, D. R.; Kobayashi, K. J. Am. Chem. Soc. 1995, 117, 12011-12012. (d) For the preparation of 4, see: Desert, S.; Metzner, P. Tetrahedron 1992, 47, 10327-10338.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 3588-3597
    • Maruoka, K.1    Itoh, T.2    Sakurai, M.3    Nonoshita, K.4    Yamamoto, H.5
  • 13
    • 0029619410 scopus 로고
    • (b) For the preparation of aldehydes involved in the synthesis of 5 and 6, see: Maruoka, K.; Itoh, T.; Sakurai, M.; Nonoshita, K.; Yamamoto, H. J. Am. Chem. Soc. 1988, 110, 3588-3597. (c) Smith, A. B., III; Qiu, Y.; Jones, D. R.; Kobayashi, K. J. Am. Chem. Soc. 1995, 117, 12011-12012. (d) For the preparation of 4, see: Desert, S.; Metzner, P. Tetrahedron 1992, 47, 10327-10338.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 12011-12012
    • Smith III, A.B.1    Qiu, Y.2    Jones, D.R.3    Kobayashi, K.4
  • 14
    • 0026454349 scopus 로고
    • (b) For the preparation of aldehydes involved in the synthesis of 5 and 6, see: Maruoka, K.; Itoh, T.; Sakurai, M.; Nonoshita, K.; Yamamoto, H. J. Am. Chem. Soc. 1988, 110, 3588-3597. (c) Smith, A. B., III; Qiu, Y.; Jones, D. R.; Kobayashi, K. J. Am. Chem. Soc. 1995, 117, 12011-12012. (d) For the preparation of 4, see: Desert, S.; Metzner, P. Tetrahedron 1992, 47, 10327-10338.
    • (1992) Tetrahedron , vol.47 , pp. 10327-10338
    • Desert, S.1    Metzner, P.2
  • 18
    • 85034465151 scopus 로고    scopus 로고
    • note
    • The relative stereochemistry of 7a and 7b was assigned by comparison with authentic samples prepared from 2a and 2b, respectively, using the following sequence: (Matrix Presented)
  • 19
    • 85034479398 scopus 로고    scopus 로고
    • note
    • The relative stereochemistry of 8a was assigned by comparison with an authentic sample prepared from 2a (see the Supporting Information).
  • 20
    • 85034470553 scopus 로고    scopus 로고
    • note
    • The relative stereochemistry of 9a and 9b was assigned by converting them to the corresponding carboxylic acid and comparison with the acid obtained from 2a by oxidation of the aromatic ring (see the Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.