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Volumn 131, Issue 13, 2009, Pages 4562-4563

Chiral brønsted acid-catalyzed enantioselective α- hydroxylation of β-dicarbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

DICARBONYL COMPOUNDS; ENANTIOCONTROL; ENANTIOSELECTIVE; NITROSO COMPOUNDS; OXYGEN SOURCES;

EID: 67749089286     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8088907     Document Type: Article
Times cited : (163)

References (35)
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    • For Lewis acid-catalyzed asymmetric hydroxylation of β-keto esters, see: a
    • For Lewis acid-catalyzed asymmetric hydroxylation of β-keto esters, see: (a) Bonaccorsi, C.; Althaus, M.; Becker, C.; Togni, A.; Mezzetti, A. Pure Appl. Chem. 2006, 78, 391.
    • (2006) Pure Appl. Chem , vol.78 , pp. 391
    • Bonaccorsi, C.1    Althaus, M.2    Becker, C.3    Togni, A.4    Mezzetti, A.5
  • 9
    • 38349189109 scopus 로고    scopus 로고
    • For selected papers, see: a
    • For selected papers, see: (a) Akiyama, T. Chem. Rev. 2007, 107, 5744.
    • (2007) Chem. Rev , vol.107 , pp. 5744
    • Akiyama, T.1
  • 13
    • 42249089542 scopus 로고    scopus 로고
    • Int. Ed, For more examples, see the Supporting Information
    • (e) Xu, S.; Wang, Z.; Zhang, X.; Ding, K. Angew. Chem., Int. Ed. 2008, 47, 2840. For more examples, see the Supporting Information.
    • (2008) Angew. Chem , vol.47 , pp. 2840
    • Xu, S.1    Wang, Z.2    Zhang, X.3    Ding, K.4
  • 16
    • 0141522552 scopus 로고    scopus 로고
    • For aminoxylation of aldehydes, see: a
    • For aminoxylation of aldehydes, see: (a) Zhong, G. Angew. Chem., Int. Ed. 2003, 42, 4247.
    • (2003) Angew. Chem., Int. Ed , vol.42 , pp. 4247
    • Zhong, G.1
  • 22
    • 1642380424 scopus 로고    scopus 로고
    • For applications of aminoxylation in tandem reactions, see: a
    • For applications of aminoxylation in tandem reactions, see: (a) Zhong, G. Chem. Commun. 2004, 606.
    • (2004) Chem. Commun , pp. 606
    • Zhong, G.1
  • 29
    • 13644253047 scopus 로고    scopus 로고
    • For a seminal work on Brønsted acid-catalyzed aminoxylation of enamines, see
    • For a seminal work on Brønsted acid-catalyzed aminoxylation of enamines, see: Momiyama, N.; Yamamoto, H. J. Am. Chem. Soc. 2005, 127, 1080.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 1080
    • Momiyama, N.1    Yamamoto, H.2
  • 30
    • 67949097975 scopus 로고    scopus 로고
    • This was confirmed by DFT calculations see the Supporting Information for details
    • This was confirmed by DFT calculations (see the Supporting Information for details).
  • 31
    • 67949105652 scopus 로고    scopus 로고
    • See the Supporting Information for more detailed experimental results
    • See the Supporting Information for more detailed experimental results.
  • 32
    • 67949116258 scopus 로고    scopus 로고
    • Control experiments under an inert atmosphere gave similar results, confirming that nitrosobenzene was the only oxygen source see the Supporting Information for a detailed mechanism investigation
    • Control experiments under an inert atmosphere gave similar results, confirming that nitrosobenzene was the only oxygen source (see the Supporting Information for a detailed mechanism investigation).
  • 33
    • 67949090267 scopus 로고    scopus 로고
    • See ref 5c
    • (a) See ref 5c.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.