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Journal ArticleDOI

Donor-acceptor-substituted cyclopropane derivatives and their application in organic synthesis.

Hans-Ulrich Reissig, +1 more
- 21 Feb 2003 - 
- Vol. 103, Iss: 4, pp 1151-1196
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This article is published in Chemical Reviews.The article was published on 2003-02-21. It has received 1211 citations till now. The article focuses on the topics: Organic synthesis & Cyclopropane.

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Citations
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A new golden age for donor-acceptor cyclopropanes.

TL;DR: This Review highlights the appropriate tools for successfully employing donor-acceptor cyclopropanes in ring-opening reactions, cycloadditions, and rearrangements.
Journal ArticleDOI

Heterocycles from cyclopropanes: applications in natural product synthesis

TL;DR: This tutorial review focuses on the latter, describing recent developments and applications of cyclopropane ring-expansion reactions in natural product synthesis and several newly developed methods providing access to densely functionalized heterocycles.
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Recent studies on the reactions of α-diazocarbonyl compounds

TL;DR: New developments of various reactions of α-diazocarbonyl compounds have been reviewed in this article, which primarily focuses on the literatures published since 2003, focusing on the literature published in 2003.
References
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Target-oriented and diversity-oriented organic synthesis in drug discovery.

TL;DR: Several synthetic planning principles for diversity-oriented synthesis and their role in the drug discovery process are presented in this review.
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Maximizing Synthetic Efficiency: Multi-Component Transformations Lead the Way

TL;DR: Over the last five years, industrial and academic researchers have made the unique exploratory power of some reactions into one of the most efficient and cost-effective tools for combinatorial and parallel synthesis.
Journal ArticleDOI

Mechanism-based target identification and drug discovery in cancer research

TL;DR: There has been a tremendous increase in the authors' knowledge of the molecular mechanisms and pathophysiology of human cancer, and many of these mechanisms have been exploited as new targets for drug development in the hope that they will have greater antitumor activity with less toxicity to the patient.
Journal ArticleDOI

Chiral semicorrins and related nitrogen heterocycles as ligands in asymmetric catalysis

TL;DR: The number of efficient, truly useful enantioselective catalysts is still limited as discussed by the authors, and the main efforts of future research will continue to focus on the improvement of existing methods and on the search for new catalysts.
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