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Domino-reactions: The tandem-knoevenagel-hetero-diels-alder reaction and its application in natural product synthesis

Lutz F. Tietze
- 01 Jan 1990 - 
- Vol. 27, Iss: 1, pp 47-69
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 1990-01-01. It has received 176 citations till now. The article focuses on the topics: Knoevenagel condensation & Diels–Alder reaction.

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Domino Reactions in Organic Synthesis

TL;DR: It is shown that domino reactions initiated by oxidation or reduction or reduction, as well as other mechanisms, can be inhibited by various materials, such as Na6(CO3)(SO4), Na2SO4, Na2CO3, and so on.
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Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis

TL;DR: Various named reactions, multi-component reactions and the synthesis of heterocyclic compounds are discussed including the use of various energy input systems such as microwave- and ultrasound irradiation, among others.
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Utilisation of 1,3‐Dicarbonyl Derivatives in Multicomponent Reactions

TL;DR: In this article, an overview of the potential of 1,3-dicarbonyl derivatives for the selective construction of highly functionalised small organic molecules of high synthetic and biological value is presented.
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Multicomponent domino reactions for the synthesis of biologically active natural products and drugs.

TL;DR: The synthesis of the enantiopure alkaloid (−)‐hirsutine 22, which has a strong inhibitorial effect on influenza A viruses, was accomplished using a biomimetic domino Knoevenagel‐hetero‐Diels Alder‐solvolysis‐hydrogenation process.
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Sequentielle Transformationen in der Organischen Chemie eine Synthesestrategie mit Zukunft

TL;DR: The organisch-chemische Synthese hat stets eine grose Faszination auf den Chemiker ausgeubt, und sie wird auch in Zukunft nichts von ihrer Bedeutung verlieren as discussed by the authors.
References
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Mechanistic Aspects of Diels‐Alder Reactions: A Critical Survey

TL;DR: In this paper, a line of distinction between the mechanistic alternatives for the Diels-Alder reaction was drawn, considering all experimental and theoretical criteria, for one-step and two-step reactions.