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Volumn 136, Issue 26, 2014, Pages 9471-9476

Rh(I)-catalyzed intermolecular hydroacylation: Enantioselective cross-coupling of aldehydes and ketoamides

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; ENANTIOSELECTIVITY; ORGANIC COMPOUNDS; RHODIUM;

EID: 84903708066     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja504296x     Document Type: Article
Times cited : (55)

References (80)
  • 1
  • 5
    • 0024073234 scopus 로고
    • For an industrial application of carbonyl hydroacylation (Tishchenko reaction), see
    • For an industrial application of carbonyl hydroacylation (Tishchenko reaction), see: Ulrich, D.; Jankowski, H. Chem. Tech. 1988, 40, 393
    • (1988) Chem. Tech. , vol.40 , pp. 393
    • Ulrich, D.1    Jankowski, H.2
  • 8
    • 0025401154 scopus 로고
    • For an early example of intramolecular ketone hydroacylation catalyzed by an achiral rhodium complex, see
    • For an early example of intramolecular ketone hydroacylation catalyzed by an achiral rhodium complex, see: Bergens, S. H.; Fairlie, D. P.; Bosnich, B. Organometallics 1990, 9, 566
    • (1990) Organometallics , vol.9 , pp. 566
    • Bergens, S.H.1    Fairlie, D.P.2    Bosnich, B.3
  • 20
    • 84903738584 scopus 로고    scopus 로고
    • See ref 4.
    • See ref 4.
  • 38
    • 84857230364 scopus 로고    scopus 로고
    • For a selenide-catalyzed cross-Tishchenko reaction, see
    • For a selenide-catalyzed cross-Tishchenko reaction, see: Curran, S. P.; Connon, S. J. Org. Lett. 2012, 14, 1074
    • (2012) Org. Lett. , vol.14 , pp. 1074
    • Curran, S.P.1    Connon, S.J.2
  • 41
    • 0037451090 scopus 로고    scopus 로고
    • The trans -effect of unsymmetrical bidentate ligands in Pd-catalyzed allylic substitutions has been reported
    • The trans -effect of unsymmetrical bidentate ligands in Pd-catalyzed allylic substitutions has been reported: Tu, T.; Zhou, Y.-G.; Hou, X.-L.; Dai, L.-X.; Dong, X.-C.; Yu, Y.-H.; Sun, J. Organometallics 2003, 22, 1255
    • (2003) Organometallics , vol.22 , pp. 1255
    • Tu, T.1    Zhou, Y.-G.2    Hou, X.-L.3    Dai, L.-X.4    Dong, X.-C.5    Yu, Y.-H.6    Sun, J.7
  • 43
    • 31444451709 scopus 로고    scopus 로고
    • Measures were taken to ensure that the reported ee is representative of the reaction and not an artifact of self-disproportionation of enantiomers (see Supporting Information). For an example of self-disproportionation of enantiomers during achiral phase silica gel chromatography, see
    • Measures were taken to ensure that the reported ee is representative of the reaction and not an artifact of self-disproportionation of enantiomers (see Supporting Information). For an example of self-disproportionation of enantiomers during achiral phase silica gel chromatography, see: Soloshonok, V. A. Angew. Chem., Int. Ed. 2006, 45, 766
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 766
    • Soloshonok, V.A.1
  • 76
    • 84892140949 scopus 로고    scopus 로고
    • For an example of rhodium behaving as a dual-role catalyst, see
    • For an example of rhodium behaving as a dual-role catalyst, see: Dornan, P. K.; Kou, K. G. M.; Houk, K. N.; Dong, V. M. J. Am. Chem. Soc. 2014, 136, 291
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 291
    • Dornan, P.K.1    Kou, K.G.M.2    Houk, K.N.3    Dong, V.M.4
  • 80
    • 84903738209 scopus 로고    scopus 로고
    • See ref 4
    • See ref 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.