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Volumn 68, Issue 6, 1985, Pages 1592-1604

Asymmetrische Michael‐Additionen. Stereoselektive Alkylierung chiraler, nicht racemischer Enolate durch Nitroolefine. Herstellung enantiomerenreiner γ‐Aminobuttersäure‐ und Bernsteinsäure‐Derivate

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EID: 84985606357     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.19850680611     Document Type: Article
Times cited : (142)

References (75)
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    • Asymmetrische Michael-Additionen. Stereoselektive Alkylierungen des (R)- und (S)-Enamins aus Cyclohexanon und 2-(Methoxymethyl)pyrrolidin durch α-(Methoxycarbonyl)zimtsäure-methylester
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    • Blarer, S.J.1    Seebach, D.2
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    • Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication
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    • Übersicht:, in ‘The Robert A. Welch Foundation Conferences on Chemical Research. XXVII. Stereospecifity in Chemistry and Biochemistry,’ Houston, Texas, Nov. 7–9, 1983, published in the proceedings of the above Conference, Welch Foundation, Houston
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    • Dissertation No. 7442, ETH‐Zürich
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    • Bull. Soc. Chim. Fr.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.