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Volumn 17, Issue 27, 2011, Pages 7418-7422

Substrate-controlled, phosphine-catalyzed domino reactions of activated conjugated dienes: Highly diastereoselective synthesis of bicyclic skeletons

Author keywords

domino reactions; Michael reaction; organocatalysis; phosphine; Rauhut Currier reaction

Indexed keywords

DOMINO REACTIONS; MICHAEL REACTION; ORGANOCATALYSIS; PHOSPHINE; RAUHUT-CURRIER REACTION;

EID: 79959401939     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201100881     Document Type: Article
Times cited : (58)

References (65)
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    • For general reviews of domino reactions, see
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    • For recent cross-RC reactions, see
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    • For general reviews on RC reactions, see
    • For general reviews on RC reactions, see
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    • For recent intramolecular RC reactions, see
    • For recent intramolecular RC reactions, see
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    • For recent domino reactions involving a RC reaction, see
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    • For the utility of conjugated dienes in domino reaction involving MBH-type (or RC-type) reactions, see
    • For the utility of conjugated dienes in domino reaction involving MBH-type (or RC-type) reactions, see
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    • For reviews, see
    • For reviews, see
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    • See the Supporting Information for the preliminary studies on β,γ-unsaturated-α-ketoester.
    • See the Supporting Information for the preliminary studies on β,γ-unsaturated-α-ketoester.
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    • CCDC-813918 (3 e) and 813919 (4 e) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC-813918 (3 e) and 813919 (4 e) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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    • N2' reactions, see:,. It can be also viewed as an anti-Michael addition, See
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.