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Volumn 46, Issue 46, 2010, Pages 8728-8730

1,4-Addition of silicon dienoates to α,β-unsaturated aldehydes catalyzed by in situ-generated silicon Lewis acid

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; BROMINE DERIVATIVE; BRONSTED ACID; LEWIS ACID; SILICON;

EID: 78549235063     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc02438d     Document Type: Article
Times cited : (39)

References (28)
  • 1
    • 0002573501 scopus 로고
    • To the best of our knowledge, there is only one example for Lewis acid-mediated 1,4-addition chemistry toward α,β-unsaturated aldehyde system, see:
    • K. Narasaka K. Soai T. Mukaiyama Chem. Lett. 1974 1223
    • (1974) Chem. Lett. , pp. 1223
    • Narasaka, K.1    Soai, K.2    Mukaiyama, T.3
  • 24
    • 0347504883 scopus 로고    scopus 로고
    • 12c In the previous work, we found that 3-bromo-2-TESO-furan is useful nucleophile for the anti-selective VMM reaction of β-monosubstituted α,β-unsaturated ketones, see: ref. 8b Synthetic applications of α-bromo-γ-butenolides, see:
    • A. Hasegawa K. Ishihara H. Yamamoto Angew. Chem., Int. Ed. 2003 42 5731
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5731
    • Hasegawa, A.1    Ishihara, K.2    Yamamoto, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.