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Volumn 30, Issue 13, 2000, Pages 2335-2343

A synthetic method for preparing 3,3-dialkyl-1,2,3,8-tetrahydroazulen-1- one

Author keywords

[No Author keywords available]

Indexed keywords

AZULENE DERIVATIVE;

EID: 0034038478     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397910008086874     Document Type: Article
Times cited : (10)

References (16)
  • 6
    • 0003132878 scopus 로고    scopus 로고
    • For our other efforts for the synthesis of non-substituted and 2,3-disubstituted tetrahydroazulenones by the Nazarov cyclization, see Oda, M.; Yamazaki, T.; Kajioka, T.; Miyatake, R.; Kuroda, S. Liebigs Ann. / Recueil 1997, 2563-2566; Kajioka, T.; Oda, M.; Yamada, S.; Kawamori, Y.; Miyatake, R.; Kuroda, S. Synthesis, 1999, 184-187.
    • (1997) Liebigs Ann. / Recueil , pp. 2563-2566
    • Oda, M.1    Yamazaki, T.2    Kajioka, T.3    Miyatake, R.4    Kuroda, S.5
  • 7
    • 0032907450 scopus 로고    scopus 로고
    • For our other efforts for the synthesis of non-substituted and 2,3-disubstituted tetrahydroazulenones by the Nazarov cyclization, see Oda, M.; Yamazaki, T.; Kajioka, T.; Miyatake, R.; Kuroda, S. Liebigs Ann. / Recueil 1997, 2563-2566; Kajioka, T.; Oda, M.; Yamada, S.; Kawamori, Y.; Miyatake, R.; Kuroda, S. Synthesis, 1999, 184-187.
    • (1999) Synthesis , pp. 184-187
    • Kajioka, T.1    Oda, M.2    Yamada, S.3    Kawamori, Y.4    Miyatake, R.5    Kuroda, S.6
  • 8
    • 0002551695 scopus 로고
    • Vogel, E.; Feldmann, R.; Düwel, H. Tetrahedron Lett., 1970, 1941-1944; Higuchi, H.; Kondo, M.; Yonehara, J.; Ojima, J.; Iyoda, M. Bull. Chem. Soc. Jpn., 1993, 66, 275-281.
    • (1970) Tetrahedron Lett. , pp. 1941-1944
    • Vogel, E.1    Feldmann, R.2    Düwel, H.3
  • 11
    • 0002571701 scopus 로고
    • (Ed. by Vedejs, E.), John Wiley & Sons, New York
    • Mukaiyama, T.; Narasaka, K "Organic Syntheses," Vol. 65 (Ed. by Vedejs, E.), John Wiley & Sons, New York, 1987, pp 6-11.
    • (1987) Organic Syntheses , vol.65 , pp. 6-11
    • Mukaiyama, T.1    Narasaka, K.2
  • 12
    • 85077851569 scopus 로고
    • Santelli-Rouvier, C.; Santelli, M. Synthesis, 1983, 429-442; Denmark, S. "Comprehensive Organic Synthesis," Ed. by Trost, B. M.; Fleming, I., Pergamon, Oxford, 1991, Vol. 5, Chap, 6.3, pp 751-784; Habermas, K. L.; Denmark, S.; Jones, T. K. Org. React., 1994, 45, 1-158.
    • (1983) Synthesis , pp. 429-442
    • Santelli-Rouvier, C.1    Santelli, M.2
  • 13
    • 0000646877 scopus 로고
    • Ed. by Trost, B. M.; Fleming, I., Pergamon, Oxford, Chap, 6.3
    • Santelli-Rouvier, C.; Santelli, M. Synthesis, 1983, 429-442; Denmark, S. "Comprehensive Organic Synthesis," Ed. by Trost, B. M.; Fleming, I., Pergamon, Oxford, 1991, Vol. 5, Chap, 6.3, pp 751-784; Habermas, K. L.; Denmark, S.; Jones, T. K. Org. React., 1994, 45, 1-158.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 751-784
    • Denmark, S.1
  • 14
    • 0001992172 scopus 로고
    • Santelli-Rouvier, C.; Santelli, M. Synthesis, 1983, 429-442; Denmark, S. "Comprehensive Organic Synthesis," Ed. by Trost, B. M.; Fleming, I., Pergamon, Oxford, 1991, Vol. 5, Chap, 6.3, pp 751-784; Habermas, K. L.; Denmark, S.; Jones, T. K. Org. React., 1994, 45, 1-158.
    • (1994) Org. React. , vol.45 , pp. 1-158
    • Habermas, K.L.1    Denmark, S.2    Jones, T.K.3
  • 15
    • 85037964335 scopus 로고    scopus 로고
    • note
    • 9 it is surprising that the cyclization of β-hydroxyethylvinyl ketones via dehydration has not been reported except an example of aryl-β-hydroxyethyl ketones.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.