Ring Forming Approaches to para-Quinones: Toward a General Diels–Alder Disconnection

Autor: Christopher G. Newton, Jessica E. Budwitz

Publikováno v: Synlett. 33:1473-1480

para-Quinones feature extensively as targets and/or intermediates throughout a number of chemical and biological subdisciplines, highlighting the importance of efficient preparative methods. This Synpacts article provides an overview of ring forming

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e9483505cb7adb3c83eebe2cfbd097fc
https://doi.org/10.1055/s-0041-1737966

Visible‐Light Photoredox Catalysis Enables the Biomimetic Synthesis of Nyingchinoids A, B, and D, and Rasumatranin D

Autor: Jonathan H. George, David M. Huang, Christopher G. Newton, Aaron J. Day, Christopher J. Sumby, Jacob D. Hart, Laura Burchill

Publikováno v: Angewandte Chemie International Edition. 58:2791-2794

The total synthesis of nyingchinoids A and B has been achieved through successive rearrangements of a 1,2-dioxane intermediate that was assembled using a visible-light photoredox-catalysed aerobic [2+2+2] cycloaddition. Nyingchinoid D was synthesised

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012ed58af60ddb361f0722253b6aee27
https://doi.org/10.1002/anie.201814089

Chiral Cp Ligands for Rhodium(III)-Catalyzed Asymmetric Carbon-Hydrogen Bond Functionalization

Autor: Christopher G. Newton, Nicolai Cramer

Publikováno v: Rhodium Catalysis in Organic Synthesis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e26e85b8295b43aefad00be7709fda2c
https://doi.org/10.1002/9783527811908.ch21

Total synthesis of the pseudopterosin aglycones

Autor: Michael S. Sherburn, Christopher G. Newton

Publikováno v: Natural Product Reports. 32:865-876

Covering up to 2015 The pseudopterosin natural products have been the focus of a substantial number of synthetic studies since the first members were isolated almost 30 years ago. Herein we review all total and formal syntheses of this family of glyc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e0edd9e2f37a1bffb2d634cef453b4f
https://doi.org/10.1039/c5np00008d

Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions

Autor: Samuel L. Drew, Christopher G. Newton, Anthony C. Willis, Andy Lawrence, Michael N. Paddon-Row, Michael S. Sherburn

Publikováno v: Newton, C G, Drew, S L, Lawrence, A L, Willis, A C, Paddon-Row, M N & Sherburn, M S 2015, ' Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions ', Nature Chemistry, vol. 7, pp. 82-86 . https://doi.org/10.1038/NCHEM.2112

The pseudopterosins are a family of diterpene marine natural products, which, by virtue of their interesting anti-inflammatory and analgesic properties, have attracted the attentions of many synthetic chemists. The most efficient syntheses reported t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e84ad8ef9e829bff37573e7992044c6
https://doi.org/10.1038/nchem.2112