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Volumn 133, Issue 3, 2011, Pages 406-408

Silylene-mediated polarity reversal of dienoates: Additions of dienoates to aldehydes at the δ-position to form trans-dioxasilacyclononenes

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL AUXILIARIES; FUNCTIONALIZATIONS; NUCLEOPHILIC CENTERS; POLARITY REVERSAL; PURE MATERIALS; SILYLENES; STEREOSPECIFICITY; TRANSITION STATE; UNSATURATED CARBONYL COMPOUNDS;

EID: 79851499673     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja109631z     Document Type: Article
Times cited : (27)

References (32)
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    • For a recent review of 1,6-additions to enoates, see, and references therein
    • For a recent review of 1,6-additions to enoates, see: Fukuhara, K.; Urabe, H. Tetrahedron Lett. 2005, 46, 603-606, and references therein.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 603-606
    • Fukuhara, K.1    Urabe, H.2
  • 7
    • 33947291143 scopus 로고
    • The dissolving metal reduction of a dienone resulted in protonation at the d-position
    • The dissolving metal reduction of a dienone resulted in protonation at the d-position: Grimm, K.; Venkataramani, P. S.; Reusch, W. J. Am. Chem. Soc. 1971, 93, 270-271.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 270-271
    • Grimm, K.1    Venkataramani, P.S.2    Reusch, W.3
  • 8
    • 0030457121 scopus 로고    scopus 로고
    • Crotylsilanes bearing carbonyl groups also give products that resemble electrophilic addition at the d-position
    • Crotylsilanes bearing carbonyl groups also give products that resemble electrophilic addition at the d-position: Jain, N. F.; Takenaka, N.; Panek, J. S. J. Am. Chem. Soc. 1996, 118, 12475-12476.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12475-12476
    • Jain, N.F.1    Takenaka, N.2    Panek, J.S.3
  • 11
    • 84875235318 scopus 로고    scopus 로고
    • The relative configurations of cyclononenes 5 and 7 were determined by NOE correlations
    • The relative configurations of cyclononenes 5 and 7 were determined by NOE correlations.
  • 13
    • 0343778881 scopus 로고
    • For reviews, see
    • For reviews, see: Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293-1316.
    • (1995) Chem. Rev. , vol.95 , pp. 1293-1316
    • Masse, C.E.1    Panek, J.S.2
  • 16
    • 0000784961 scopus 로고
    • For different methods for activation of silicon centers, see
    • For different methods for activation of silicon centers, see: Matsumoto, K.; Oshima, K.; Utimoto, K. J. Org. Chem. 1994, 59, 7152-7155.
    • (1994) J. Org. Chem. , vol.59 , pp. 7152-7155
    • Matsumoto, K.1    Oshima, K.2    Utimoto, K.3
  • 24
    • 0000145196 scopus 로고
    • Dauben, W. G. Ed.; Wiley-VCH: Weinheim
    • Mukaiyama, T. In Organic Reactions; Dauben, W. G. Ed.; Wiley-VCH: Weinheim, 1982; Vol. 28, pp 203-331.
    • (1982) Organic Reactions , vol.28 , pp. 203-331
    • Mukaiyama, T.1
  • 25
    • 84875274498 scopus 로고    scopus 로고
    • The relative configurations of cyclononenes 10 and 21 were determined by X-ray crystallography
    • The relative configurations of cyclononenes 10 and 21 were determined by X-ray crystallography.
  • 26
    • 0037009989 scopus 로고    scopus 로고
    • Allylborations can also be accelerated by Lewis acids
    • Allylborations can also be accelerated by Lewis acids: Kennedy, J. W. J.; Hall, D. G. J. Am. Chem. Soc. 2002, 124, 11586-11587.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11586-11587
    • Kennedy, J.W.J.1    Hall, D.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.