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Volumn 137, Issue 9, 2015, Pages 3201-3204

Rhodium-catalyzed asymmetric arylation of allyl sulfones under the conditions of isomerization into alkenyl sulfones

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CATALYSIS; CHEMICAL REACTIONS; ENANTIOSELECTIVITY; ISOMERIZATION; ISOMERS;

EID: 84924662551     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b00216     Document Type: Article
Times cited : (52)

References (59)
  • 31
    • 15844367249 scopus 로고
    • Trost, B. M. Fleming, I. Pergamon: Oxford
    • Kelly, S. E. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 1, p 792.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 792
    • Kelly, S.E.1
  • 50
    • 0034715487 scopus 로고    scopus 로고
    • This is assumed to be formed through a reaction pathway involving the 1,4-shift of rhodium from an alkyl-Rh intermediate to an ortho -alkylaryl-Rh intermediate. As a key reference: see
    • This is assumed to be formed through a reaction pathway involving the 1,4-shift of rhodium from an alkyl-Rh intermediate to an ortho -alkylaryl-Rh intermediate. As a key reference: see Oguma, K.; Miura, M.; Satoh, T.; Nomura, M. J. Am. Chem. Soc. 2000, 122, 10464
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10464
    • Oguma, K.1    Miura, M.2    Satoh, T.3    Nomura, M.4
  • 57
    • 0141450342 scopus 로고    scopus 로고
    • The rationalization of stereochemical pathway using this type of model has been always successful (ref 17b). See also
    • The rationalization of stereochemical pathway using this type of model has been always successful (ref 17b). See also, Hayashi, T.; Ueyama, K.; Tokunaga, N.; Yoshida, K. J. Am. Chem. Soc. 2003, 125, 11508
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 11508
    • Hayashi, T.1    Ueyama, K.2    Tokunaga, N.3    Yoshida, K.4
  • 59
    • 0028913777 scopus 로고
    • In our experiments (with DBU in THF at 25 °C), the equilibrated ratio was 25/75 for 9/10
    • Berranger, T.; Langlois, Y. J. Org. Chem. 1995, 60, 1720 In our experiments (with DBU in THF at 25 °C), the equilibrated ratio was 25/75 for 9/10
    • (1995) J. Org. Chem. , vol.60 , pp. 1720
    • Berranger, T.1    Langlois, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.