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Volumn 9, Issue 9, 1998, Pages 1619-1626

Enantioselective synthesis of 2-allyl and 2-(3- trimethylsilylpropargyl)-2-hydroxycyclohexanone using osmium-catalyzed asymmetric dihydroxylation

Author keywords

[No Author keywords available]

Indexed keywords

2 (3 TRIMETHYLSILYLPROPARGYL) 2 HYDROXYCYCLOHEXANONE; 2 ALLYL 2 HYDROXYCYCLOHEXANONE; CYCLOHEXANONE DERIVATIVE; OSMIUM; UNCLASSIFIED DRUG;

EID: 0032496253     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00144-X     Document Type: Article
Times cited : (9)

References (24)
  • 9
    • 84918476418 scopus 로고
    • Wiley, New York, Third edition, chapter 18
    • (a) March, J. In Advanced Organic Chemistry, Wiley, New York, Third edition, 1985, chapter 18, p. 968;
    • (1985) Advanced Organic Chemistry , pp. 968
    • March, J.1
  • 17
    • 0027465280 scopus 로고
    • For improvements of the AD reaction see: (a) Sharpless, K. B.; Amberg, W.; Bennani, Y. L.; Crispino, G. A.; Hartung, J.; Jeong, K. S.; Kwong, H. L.; Morikawa, K.; Wang, Z. M.; Xu, D. and Zhang, X. L. J. Org. Chem. 1992, 57, 2768-2771; (b) Bennani, Y. L. and Sharpless, K. B. Tetrahedron Lett. 1993, 34, 2079-2082.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 2079-2082
    • Bennani, Y.L.1    Sharpless, K.B.2
  • 21
    • 0345484719 scopus 로고    scopus 로고
    • note
    • 3e
  • 24
    • 0344622533 scopus 로고    scopus 로고
    • note
    • Indeed, the acetonide 17 can be transformed by the same reaction sequence as for 7 to the analog of the α-aminoketone 2b, which by palladium-promoted endo-azacyclization, unpublished method developed in our laboratory, will furnish the lactam 19.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.