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Volumn 132, Issue 10, 2010, Pages 3262-3263

Chiral silver amide-catalyzed enantioselective [3 + 2] cycloaddition of α-aminophosphonates with olefins

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE COMPLEXES; AMINOPHOSPHONATES; CYCLOADDITIONS; ENANTIOSELECTIVE; HIGH YIELD; SCHIFF BASIS; SEGPHOS;

EID: 77950462377     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja100101n     Document Type: Article
Times cited : (90)

References (42)
  • 1
    • 51049115331 scopus 로고    scopus 로고
    • Recent reviews of chiral silver catalysts: (a)Naodovic, M.; Yamamoto, H. Chem. Rev. 2008, 108, 3132.
    • (2008) Chem. Rev. , vol.108 , pp. 3132
    • Naodovic, M.1    Yamamoto, H.2
  • 40
    • 0002461063 scopus 로고    scopus 로고
    • Experimental details for the formation of AgHMDS are given in the Supporting Information. Also see
    • Experimental details for the formation of AgHMDS are given in the Supporting Information. Also see: Hitchcock, P. B.; Lappert, M. F.; Pierssens, L. J.-M. Chem. Commun. 1996, 1189.
    • (1996) Chem. Commun. , pp. 1189
    • Hitchcock, P.B.1    Lappert, M.F.2    Pierssens, L.J.-M.3
  • 41
    • 77950515573 scopus 로고    scopus 로고
    • The relative and absolute configurations of the products were determined by X-ray crystallographic analysis (see the Supporting Information)
    • The relative and absolute configurations of the products were determined by X-ray crystallographic analysis (see the Supporting Information).
  • 42
    • 77950502557 scopus 로고    scopus 로고
    • The assumed transition state models are shown in the Supporting Information
    • The assumed transition state models are shown in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.