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Journal ArticleDOI

Carbocycles from donor–acceptor cyclopropanes

TLDR
This review summarizes research directed towards the formation of carbocyclic adducts from donor-acceptor cyclopropanes and focuses on annulation and cycloaddition reactions mediated by Lewis or protic acid, bases, or thermal conditions.
Abstract
This review summarizes research directed towards the formation of carbocyclic adducts from donor–acceptor cyclopropanes. The focus of the review is on annulation and cycloaddition reactions (both inter- and intramolecularly) mediated by Lewis or protic acid, bases, or thermal conditions. Rearrangements resulting in carbocycles and those reactions mediated by transition metal catalysis have been excluded.

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Application of oxygen/nitrogen substituted donor-acceptor cyclopropanes in the total synthesis of natural products

TL;DR: In this paper, a review summarises the applications of heteroatom substituted donor-acceptor cyclopropanes in the total synthesis of natural products, including cycloaddition, rearrangement and cascade reactions.
Journal ArticleDOI

Recent Advances in Ring-opening of Donor Acceptor Cyclopropanes using C-Nucleophiles

TL;DR: Ring-opening transformations of donor-acceptor cyclopropanes (DAC) with carbon-centered nucleophiles is a simple, straight-forward approach to 1,3-bifunctional compounds that has witnessed remarkable progress over the past several years.
Journal ArticleDOI

Divergent Reactivity of Thioalkynes in Lewis Acid Catalyzed Annulations with Donor-Acceptor Cyclopropanes.

TL;DR: New annulation reactions of thioalkynes with phthalimide-substituted donor-acceptor cyclopropanes gave access to highly substituted cyclopentenes and polycyclic ring systems.
Journal ArticleDOI

Lewis Acid Catalyzed Enantioselective Desymmetrization of Donor-Acceptor meso-Diaminocyclopropanes.

TL;DR: The first Lewis acid catalyzed enantioselective ring-opening desymmetrization of a donor-acceptor meso-diaminocyclopropane is reported, which delivered enantioenriched, diastereomerically pure urea products.
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Multicomponent 1,3-Bifunctionalization of Donor-Acceptor Cyclopropanes with Arenes and Nitrosoarenes.

TL;DR: AlBr3-mediated multicomponent 1,3-bifunctionalization of donor-acceptor cyclopropanes using arenes and nitrosoarenes as coupling partners is presented and the γ,γ-disubstituted N-arylated α-amino esters obtained as products are readily further chemically modified rendering the method valuable.
References
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Journal ArticleDOI

Telmisartan, Ramipril, or Both in Patients at High Risk for Vascular Events

TL;DR: Telmisartan was equivalent to ramipril in patients with vascular disease or high-risk diabetes and was associated with less angioedema and a increased risk of hypotensive symptoms.
Journal ArticleDOI

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.
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