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Volumn , Issue 2, 2008, Pages 308-318

Asymmetric Diels-Alder reaction of aminodienes with a nonracemic acrylate bound to rink resin: A comparison of these reactions with their solution-state analogues

Author keywords

Asymmetric synthesis; Chiral auxiliaries; Cyclic amino acids; Diels Alder reactions; Microwave activation; Supported synthesis

Indexed keywords


EID: 38349142808     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200700677     Document Type: Article
Times cited : (14)

References (60)
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    • When this experiment was carried out at 60°C, no reproducible results were obtained due to the heterogeneous reaction medium; the melting point of the diene is 72°C.
    • When this experiment was carried out at 60°C, no reproducible results were obtained due to the heterogeneous reaction medium; the melting point of the diene is 72°C.
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    • [13c]
    • [13c]
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    • Determined by chiral HPLC analysis as described in the Exp. Section
    • Determined by chiral HPLC analysis as described in the Exp. Section.
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    • These bicyclic amino acids have only one asymmetric carbon atom
    • These bicyclic amino acids have only one asymmetric carbon atom.
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    • for one of the few examples of previous uses of Wilkinson's catalyst for hydrogenation on solid supports, see: A. Speicher, T. Backes, S. Grosse, Tetrahedron 2005, 61, 11692-11696.
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    • It has been reported that the reaction rate of the hydrogenation of olefins catalyzed by Wilkinson's catalyst can be influenced by solvents
    • It has been reported that the reaction rate of the hydrogenation of olefins catalyzed by Wilkinson's catalyst can be influenced by solvents.
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    • The optical rotation of the free β-amino acid 23 obtained after hydrogenolysis of compound (3′ R,2R)-22c is in good accord with the value previously measured, see ref.[13d
    • [13d]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.