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Volumn , Issue 4, 1999, Pages 823-835

Diastereoselective ring expansion rearrangements of (Benzocyclobutenone)-and (Benzocyclobutenedione)chromium complexes: Syntheses of substituted 1-indanone and 1,3-indandione complexes

Author keywords

(Arene)chromium complexes; Benzocyclobutenes; Indanone derivatives; Vinylcyclobutene cyclohexadiene rearrangement; Ketol rearrangement

Indexed keywords

(BENZOCYCLOBUTENEDIONE)CHROMIUM COMPLEX; (BENZOCYCLOBUTENONE)CHROMIUM COMPLEX; ANION; CHROMIUM DERIVATIVE; INDANONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032856660     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0690(199904)1999:4<823::AID-EJOC823>3.0.CO;2-R     Document Type: Article
Times cited : (19)

References (38)
  • 1
    • 0001744040 scopus 로고
    • H. G. Wey, H. Butenschön, Angew. Chem. 1991, 103, 871-873; Angew. Chem. Int. Ed. Engl. 1991, 30, 880-881.
    • (1991) Angew. Chem. , vol.103 , pp. 871-873
    • Wey, H.G.1    Butenschön, H.2
  • 2
    • 33748217432 scopus 로고
    • H. G. Wey, H. Butenschön, Angew. Chem. 1991, 103, 871-873; Angew. Chem. Int. Ed. Engl. 1991, 30, 880-881.
    • (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 880-881
  • 5
    • 0025213988 scopus 로고
    • E. P. Kündig, G. Bernardinelli, J. Leresche, P. Romanens, Angew. Chem. 1990, 102, 421-423; Angew. Chem. Int. Ed. Engl. 1990, 29, 407-409.
    • (1990) Angew. Chem. Int. Ed. Engl. , vol.29 , pp. 407-409
  • 10
    • 33748218848 scopus 로고
    • M. Brands, R. Goddard, H. G. Wey, H. Butenschön, Angew. Chem. 1993, 105, 285-287; Angew. Chem. Int. Ed. Engl. 1993, 32, 267-269.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 267-269
  • 17
    • 0344759439 scopus 로고    scopus 로고
    • Dissertation, Universität Hannover
    • D. Leinweber, Dissertation, Universität Hannover, 1998.
    • (1998)
    • Leinweber, D.1
  • 18
    • 0001728892 scopus 로고
    • D. Seebach, Angew. Chem. 1979, 91, 259-278; Angew. Chem. Int. Ed. Engl. 1979, 18, 239-258.
    • (1979) Angew. Chem. , vol.91 , pp. 259-278
    • Seebach, D.1
  • 19
    • 0018454939 scopus 로고
    • D. Seebach, Angew. Chem. 1979, 91, 259-278; Angew. Chem. Int. Ed. Engl. 1979, 18, 239-258.
    • (1979) Angew. Chem. Int. Ed. Engl. , vol.18 , pp. 239-258
  • 27
    • 0344759438 scopus 로고
    • Dissertation, Ruhr-Universität Bochum
    • M. Brands, Dissertation, Ruhr-Universität Bochum, 1993.
    • (1993)
    • Brands, M.1
  • 30
    • 0345189823 scopus 로고    scopus 로고
    • note
    • The enantiomers of 1 were separated on a scale of a few 100 mg by HPLC using a Daicel OJ column (ee > 99%).
  • 31
    • 0344327413 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess was determined in cooperation with Prof. Dr. W. A. König, Hamburg, by GC on a cyclodextrin column (25 m, Lipodex E).
  • 36
    • 0345621962 scopus 로고    scopus 로고
    • note
    • The relative configuration of 32 was assigned in analogy with that of 33, which was verified by an X-ray structure analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.