Irreversibleendo-Selective Diels-Alder Reactions of Substituted Alkoxyfurans: A General Synthesis ofendo-Cantharimides-Reference-Cited by-同舟云学术

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Irreversibleendo-Selective Diels-Alder Reactions of Substituted Alkoxyfurans: A General Synthesis ofendo-Cantharimides

Published:2015-03-10 Issue:16 Volume:21 Page:6107-6114
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Foster Robert W.,Benhamou Laure,Porter Michael J.,Bučar Dejan-Krešimir,Hailes Helen C.,Tame Christopher J.,Sheppard Tom D.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201406286/fullpdf

Reference112 articles.

1. Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success

2. Chemical space as a source for new drugs

3. 970 Million Druglike Small Molecules for Virtual Screening in the Chemical Universe Database GDB-13

4. The impact of aromatic ring count on compound developability – are too many aromatic rings a liability in drug design?

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3. Advances in Diels–Alder/aromatization of biomass furan derivatives towards renewable aromatic hydrocarbons;Catalysis Science & Technology;2022

4. Mechanically Triggered Release of Functionally Diverse Molecular Payloads from Masked 2-Furylcarbinol Derivatives;ACS Central Science;2021-07-14

5. Potential use of the Diels-Alder reaction in biomedical and nanomedicine applications;International Journal of Pharmaceutics;2021-07

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