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Volumn 12, Issue 8, 2014, Pages 1258-1264

Organocatalytic enantioselective hydrophosphonylation of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVE; HIGH ENANTIOSELECTIVITY; HYDROPHOSPHONYLATION; MILD REACTION CONDITIONS; ORGANOCATALYTIC; PHOSPHONATES;

EID: 84893231190     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob42403k     Document Type: Article
Times cited : (43)

References (71)
  • 19
    • 0034499290 scopus 로고    scopus 로고
    • For the pioneering enantioselective hydrophosphonylation of aldehydes using metal catalysts, see
    • J. Huang R. Chen Heteroat. Chem. 2000 11 480
    • (2000) Heteroat. Chem. , vol.11 , pp. 480
    • Huang, J.1    Chen, R.2
  • 46
    • 67749124294 scopus 로고    scopus 로고
    • For organocatalytic enantioselective examples of addition using ketones, see also
    • D. Uraguchi T. Ito T. Ooi J. Am. Chem. Soc. 2009 131 3836
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3836
    • Uraguchi, D.1    Ito, T.2    Ooi, T.3
  • 62
    • 84891572262 scopus 로고    scopus 로고
    • in, ed. B. Pignataro, Wiley-VCH, 175-199 See ESI for additional results CCDC () and CCDC 953499 (4eg) contain the supplementary crystallographic data for this paper For interesting reviews, see
    • E. Marqués-López and R. P. Herrera, in New Strategies in Chemical Synthesis and Catalysis, ed., B. Pignataro, Wiley-VCH, 2012, pp. 175-199
    • (2012) New Strategies in Chemical Synthesis and Catalysis , vol.4
    • Marqués-López, E.1    Herrera, R.P.2
  • 67
    • 33847090059 scopus 로고
    • We were not able to achieve good results in terms of enantioselectivity in our model reaction neither using the same catalyst (quinine) employed by Wynberg and co-workers 10 nor using cinchonidine. 17 For a further transesterification extending the scope, see
    • B. Springs P. Haake J. Org. Chem. 1977 42 472
    • (1977) J. Org. Chem. , vol.42 , pp. 472
    • Springs, B.1    Haake, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.