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Volumn , Issue 12, 2002, Pages 2015-2018

Chromium(II)-catalyzed diastereoselective pinacol type cross coupling between α,β-unsaturated carbonyl compounds and aliphatic aldehydes

Author keywords

C C coupling; Catalysis; Chromium; Cross coupling; Pinacols

Indexed keywords

ACROLEIN DERIVATIVE; ALDEHYDE; CARBONYL DERIVATIVE; CHROMIUM; CHROMIUM CHLORIDE; KETONE DERIVATIVE; NATURAL PRODUCT;

EID: 0036456497     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-35572     Document Type: Article
Times cited : (23)

References (28)
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    • For reviews on C-C bond formation involving organochromium reagents see: (a) Fürstner, A. Chem. Rev. 1999, 99, 991. (b) Wessjohann, L. A.; Scheid, G. Synthesis 1999, 1.
    • (1999) Chem. Rev. , vol.99 , pp. 991
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    • 0032954123 scopus 로고    scopus 로고
    • For reviews on C-C bond formation involving organochromium reagents see: (a) Fürstner, A. Chem. Rev. 1999, 99, 991. (b) Wessjohann, L. A.; Scheid, G. Synthesis 1999, 1.
    • (1999) Synthesis , pp. 1
    • Wessjohann, L.A.1    Scheid, G.2
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    • 2d
    • 2d
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    • 3 and: (a) Buse, C. T.; Heathcock, C. H. Tetrahedron Lett. 1978, 19, 1685. (b) Hiyama, T.; Kimura, K.; Nozaki, H. Tetrahedron Lett. 1981, 22, 1037. (c) Jubert, C.; Nowotny, S.; Kornemann, D.; Antes, I.; Tucker, C. E.; Knochel, P. J. Org. Chem. 1992, 57, 6384. (d) Nowotny, S.; Tucker, C. E.; Jubert, C.; Knochel, P. J. Org. Chem. 1995, 60, 2762.
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    • 3 and: (a) Buse, C. T.; Heathcock, C. H. Tetrahedron Lett. 1978, 19, 1685. (b) Hiyama, T.; Kimura, K.; Nozaki, H. Tetrahedron Lett. 1981, 22, 1037. (c) Jubert, C.; Nowotny, S.; Kornemann, D.; Antes, I.; Tucker, C. E.; Knochel, P. J. Org. Chem. 1992, 57, 6384. (d) Nowotny, S.; Tucker, C. E.; Jubert, C.; Knochel, P. J. Org. Chem. 1995, 60, 2762.
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  • 22
    • 0001568428 scopus 로고
    • 3 and: (a) Buse, C. T.; Heathcock, C. H. Tetrahedron Lett. 1978, 19, 1685. (b) Hiyama, T.; Kimura, K.; Nozaki, H. Tetrahedron Lett. 1981, 22, 1037. (c) Jubert, C.; Nowotny, S.; Kornemann, D.; Antes, I.; Tucker, C. E.; Knochel, P. J. Org. Chem. 1992, 57, 6384. (d) Nowotny, S.; Tucker, C. E.; Jubert, C.; Knochel, P. J. Org. Chem. 1995, 60, 2762.
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    • note
    • The substituted acroleins can be easily prepared by Mannich reaction starting with the corresponding aldehyde.
  • 26
    • 0012017064 scopus 로고    scopus 로고
    • note
    • 3, 100 MHz) δ 159.1, 109.7, 75.1, 72.6, 35.7, 29.1, 24.3, 10.3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.