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Volumn 72, Issue 11, 2007, Pages 4093-4097

Enantioselective epoxidation of conjugated cis-enynes by chiral dioxirane

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLIDINONE; OXONE; STEREODIFFERENTIATION;

EID: 34249778116     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070205r     Document Type: Article
Times cited : (57)

References (58)
  • 1
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    • For some examples of synthetic applications of propargyl epoxides, see: a
    • For some examples of synthetic applications of propargyl epoxides, see: (a) Alexakis, A.; Marek, I.; Mangeney, P.; Normant, J. F. Tetrahedron 1991, 47, 1677.
    • (1991) Tetrahedron , vol.47 , pp. 1677
    • Alexakis, A.1    Marek, I.2    Mangeney, P.3    Normant, J.F.4
  • 12
    • 0003544583 scopus 로고
    • For leading references on asymmetric epoxidation of enynes directed by hydroxyl groups, see: a, Ojima, I. Ed, VCH: New York, Chapter 4.1
    • For leading references on asymmetric epoxidation of enynes directed by hydroxyl groups, see: (a) Johnson, R. A.; Sharpless, K. B. In Catalytic Asymmetric Synthesis; Ojima, I. Ed.; VCH: New York, 1993; Chapter 4.1.
    • (1993) Catalytic Asymmetric Synthesis
    • Johnson, R.A.1    Sharpless, K.B.2
  • 14
    • 0026072853 scopus 로고    scopus 로고
    • For leading references on asymmetric epoxidations of cis-enynes using chiral salen-type catalysts, see: (a) Lee, N. H.; Jacobsen, E. N. Tetrahedron Lett. 1991, 32, 6533.
    • For leading references on asymmetric epoxidations of cis-enynes using chiral salen-type catalysts, see: (a) Lee, N. H.; Jacobsen, E. N. Tetrahedron Lett. 1991, 32, 6533.
  • 21
    • 0032975651 scopus 로고    scopus 로고
    • For leading reviews on chiral ketone catalyzed asymmetric epoxidations, see: a
    • For leading reviews on chiral ketone catalyzed asymmetric epoxidations, see: (a) Denmark, S. E.; Wu, Z. Synlett 1999, 847.
    • (1999) Synlett , pp. 847
    • Denmark, S.E.1    Wu, Z.2
  • 25
    • 0029860777 scopus 로고    scopus 로고
    • For examples of asymmetric epoxidation mediated by fructose-derived ketone 1, see: (a) Tu, Y, Wang, Z.-X, Shi, Y. J. Am. Chem. Soc. 1996, 118, 9806
    • For examples of asymmetric epoxidation mediated by fructose-derived ketone 1, see: (a) Tu, Y.; Wang, Z.-X.; Shi, Y. J. Am. Chem. Soc. 1996, 118, 9806.
  • 38
    • 0034703736 scopus 로고    scopus 로고
    • For asymmetric epoxidation with ketone 2a, see: (a) Tian, H.; She, X.; Shu, L.; Yu, H.; Shi, Y. J. Am. Chem. Soc. 2000, 122, 11551.
    • For asymmetric epoxidation with ketone 2a, see: (a) Tian, H.; She, X.; Shu, L.; Yu, H.; Shi, Y. J. Am. Chem. Soc. 2000, 122, 11551.
  • 51
    • 34249783023 scopus 로고    scopus 로고
    • Two examples of conjugated cis-enynes (cis-1-phenyl-3- penten-1-yne and cis-2-undecen-4-yne) were previously examined with ketone 2a (91% and 87% ee obtained repectively) (ref 7).
    • Two examples of conjugated cis-enynes (cis-1-phenyl-3- penten-1-yne and cis-2-undecen-4-yne) were previously examined with ketone 2a (91% and 87% ee obtained repectively) (ref 7).
  • 53
    • 34249810219 scopus 로고    scopus 로고
    • For a detailed discussion, see: ref 4b
    • For a detailed discussion, see: ref 4b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.