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Volumn 353, Issue 11-12, 2011, Pages 1973-1979

Enantioselective intermolecular rauhut-currier reaction of electron-deficient allenes with maleimides

Author keywords

isocupreidine ( ICD); 1,4 diazabicyclic 2.2.2 octane (DABCO); allenes; chiral butenolides; enantioselectivitve Rauhut Currier reaction; maleimides

Indexed keywords


EID: 80051966146     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201100434     Document Type: Article
Times cited : (73)

References (53)
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    • Angew. Chem. Int. Ed. 2008, 47, 4177-4179. It should be noted that although the mechanism is not proposed as a concerted process, the products are formal RC reaction products; For a review on bifunctional Cinchona organocatalysts, see
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    • Miller's group has reported that an amino acid and peptide-based organocatalyst was highly efficient in the asymmetric aza-Morita-Baylis-Hillman reaction of N-acylimine derivatives with allenoates.
    • Miller's group has reported that an amino acid and peptide-based organocatalyst was highly efficient in the asymmetric aza-Morita-Baylis-Hillman reaction of N-acylimine derivatives with allenoates., B. J. Cowen, L. B. Saunders, S. J. Miller, J. Am. Chem. Soc. 2009, 131, 6105-6107.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.