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Volumn 10, Issue 8, 2008, Pages 1605-1608

Construction of higly functionalized diazoacetoacentates via catalytic Mukaiyama-Michael reactions

Author keywords

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Indexed keywords

ACETIC ACID DERIVATIVE;

EID: 44449136163     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800298n     Document Type: Article
Times cited : (47)

References (52)
  • 2
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    • Hegedus, L. S, Ed, Per-gammon Press: New York, Chapter 5.2
    • (b) Doyle, M. P. In Comprehensive Organometallic Chemistry II; Hegedus, L. S., Ed.; Per-gammon Press: New York, 1995; Vol. 12, Chapter 5.2.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12
    • Doyle, M.P.1
  • 6
    • 0003544583 scopus 로고    scopus 로고
    • 2nd ed, Ojima, I, Ed, John Wiley & Sons: New York
    • (d) Doyle, M. P. In Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; John Wiley & Sons: New York, 2000.
    • (2000) Catalytic Asymmetric Synthesis
    • Doyle, M.P.1
  • 14
  • 32
    • 0034716526 scopus 로고    scopus 로고
    • For representative examples of Mukaiyama, Michael reactions using catalytic amounts of Lewis acids, see: (a) Matsuda, I, Makino. T, Hasegawa, Y, Itoh. K. Tetrahedron Lett. 2000, 41, 1409-1412
    • For representative examples of Mukaiyama - Michael reactions using catalytic amounts of Lewis acids, see: (a) Matsuda, I.; Makino. T.; Hasegawa, Y.; Itoh. K. Tetrahedron Lett. 2000, 41, 1409-1412.
  • 38
    • 0034721430 scopus 로고    scopus 로고
    • For representative examples of asymmetric Mukaiyama-Michael reactions using Lewis acid catalysts, see: a
    • For representative examples of asymmetric Mukaiyama-Michael reactions using Lewis acid catalysts, see: (a) Evans, D. A.; Rovis, T.; Kozlowski, M.; Dowey, C. W.; Tedrow, J. S. J. Am. Chem. Soc. 2000, 122, 9134-9142.
    • (2000) Am. Chem. Soc , vol.122 , pp. 9134-9142
    • Evans, D.A.1    Rovis, T.2    Kozlowski, M.3    Dowey, C.W.4    Tedrow, J.S.J.5
  • 49
    • 58149201705 scopus 로고    scopus 로고
    • The use of other common solvents such as chloroform, toluene, THF, and ether gave diminished yields of 6a.
    • The use of other common solvents such as chloroform, toluene, THF, and ether gave diminished yields of 6a.
  • 50
    • 58149179325 scopus 로고    scopus 로고
    • In contrast to our report of Mukaiyama reaction (ref 10), the OTMS silyl enol ether analogue of 1 gave a lower yield of 6 than did 1. The additional advantage of the OTBS silyl enol ether is its greater stability.
    • In contrast to our report of Mukaiyama reaction (ref 10), the OTMS silyl enol ether analogue of 1 gave a lower yield of 6 than did 1. The additional advantage of the OTBS silyl enol ether is its greater stability.
  • 51
    • 58149200282 scopus 로고    scopus 로고
    • Other common Michael acceptors such as α,ß-unsaturated esters, unsaturated nitriles, and unsaturated nitro compounds were found to be unreactive under the standard reaction condition
    • Other common Michael acceptors such as α,ß-unsaturated esters, unsaturated nitriles, and unsaturated nitro compounds were found to be unreactive under the standard reaction condition.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.