Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans-Reference-Cited by-同舟云学术

Alkene Dioxygenation with Malonoyl Peroxides: Synthesis of γ-Lactones, Isobenzofuranones, and Tetrahydrofurans

Published:2016-06-17 Issue:13 Volume:18 Page:3102-3105
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Alamillo-Ferrer Carla¹,Karabourniotis-Sotti Marianna¹,Kennedy Alan R.¹,Campbell Matthew²,Tomkinson Nicholas C. O.¹

Affiliation:

1. WestCHEM, Department of Pure and Applied Chemistry, Thomas Graham Building, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, United Kingdom

2. GlaxoSmithKline Medicines Research Centre, Gunnels Wood Road, Stevenage SG1 2NY, United Kingdom

Funder

Engineering and Physical Sciences Research Council

Conselho Nacional de Desenvolvimento Científico e Tecnológico

GlaxoSmithKline

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01253

Reference31 articles.

1. Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea

2. Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action

3. Privileged scaffolds for library design and drug discovery

4. Iodolactonization: Past and Present Examples

5. Halo- and selenolactonisation: the two major strategies for cyclofunctionalisation

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