ReviewChemistry (Weinheim an der Bergstrasse, Germany)2022
Transition Metal Catalyst Free Synthesis of Olefins from Organoboron Derivatives.
Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 9 citations in OpenAlex.
- Application of the Horner-Wadsworth-Emmons Olefination in the Construction ofThe Journal of organic chemistry · 2025Article
- Stereoselective Copper-Catalyzed Olefination of Imines.Angewandte Chemie (International ed. in English) · 2024Article
- A unified strategy for the synthesis of aldohexoses by boronate assisted assembly of CHChemical science · 2023Article
- Transition Metal Catalyst Free Synthesis of Olefins from Organoboron Derivatives.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Review
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
Stereoselective preparation of highly substituted olefins is still a severe challenge that requires well defined elimination precursors. Organoboron chemistry is particularly suited for the preparation of molecules with adjacent stereocenters. As organo boron substrates with leaving groups in β-position can undergo stereospecific syn- or anti-elimination, this chemistry harbors great potential for the synthesis of complex olefins. In recent years three main strategies emerged, which differ in their approach to the β-functionalized organoboron elimination precursor. (i) Stereoselective preparation of such elimination precursor can be achieved by addition of a boron-stabilized anion (d
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Registered trials
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