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Volumn 20, Issue 12, 2001, Pages 2454-2458

A new chiral at metal catalyst for enantioselective Diels-Alder reactions: Observation of isomeric intermediates

Author keywords

[No Author keywords available]

Indexed keywords

CHIRALITY; DIELS-ALDER REACTIONS; ENANTIOSELECTIVITY; ISOMERIC INTERMEDIATES; METAL CATALYSTS;

EID: 0035844903     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om0010767     Document Type: Article
Times cited : (55)

References (29)
  • 24
    • 0011592527 scopus 로고    scopus 로고
    • (d) (PAN)Ru.
  • 25
    • 0011530602 scopus 로고    scopus 로고
    • note
    • 2, 3, 3′, and 3″ were repeated numerous times. An additional peak (δ 31) was occasionally detected and is assigned to the product of partial catalyst decomposition. This assignment was made on the basis of VT NMR and SST experiments, which demonstrated that this compound was not involved in the exchange processes observed for 2, 3, 3′, and 3″.
  • 26
    • 0001256335 scopus 로고
    • King, R. B., Ed.; John Wiley and Sons: New York
    • Faller, J. W. In Encyclopedia of Inorganic Chemistry. King, R. B., Ed.; John Wiley and Sons: New York, 1994; p 3914.
    • (1994) Encyclopedia of Inorganic Chemistry , pp. 3914
    • Faller, J.W.1
  • 27
    • 0030893497 scopus 로고    scopus 로고
    • note
    • 2-coordination of aldehydes to cationic rhenium centers has also been well documented: Gladysz, J. A.; Boone, B. J. Angew. Chem., Int. Ed. Engl. 1997, 36, 550. In this case, conformational isomers probably arise from orientations of the cymene.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 550
    • Gladysz, J.A.1    Boone, B.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.