An Insight into Selective Olefin Bond Functionalization of Cyclodienes through Nitrile Oxide 1,3-Dipolar Cycloadditions-Reference-Cited by-同舟云学术

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An Insight into Selective Olefin Bond Functionalization of Cyclodienes through Nitrile Oxide 1,3-Dipolar Cycloadditions

Published:2019-03-08 Issue:10 Volume:4 Page:2886-2891
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Benke Zsanett¹²,Nonn Melinda¹³²,Fülöp Ferenc¹³²,Kiss Loránd¹²^ORCID

Affiliation:

1. Institute of Pharmaceutical Chemistry; University of Szeged; H-6720 Szeged Eötvös u. 6 Hungary

2. University of Szeged; Interdisciplinary Excellence Centre; Institute of Pharmaceutical Chemistry

3. MTA-SZTE Stereochemistry Research Group; Hungarian Academy of Sciences; H-6720 Szeged Eötvös u. 6 Hungary

Funder

Hungarian Research Foundation

GINOP

EFOP

Ministry of Human Capacities

Hungary grant

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201900688/fullpdf

Reference47 articles.

1. Scaffold Diversity Synthesis and Its Application in Probe and Drug Discovery

2. Route to three-dimensional fragments using diversity-oriented synthesis

3. A systematic approach to diverse, lead-like scaffolds from α,α-disubstituted amino acids

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1. Application of 2‐Azabicyclo[2.2.1]Hept‐5‐En‐3‐One (Vince Lactam) in Synthetic Organic and Medicinal Chemistry;The Chemical Record;2024-07-15

2. A computational study of 1,3-dipolar cycloadditions of nitrile oxides with dienes;Tetrahedron;2023-06

3. Diversity-Oriented Synthesis of Highly Functionalized Alicycles across Dipolar Cycloaddition/Metathesis Reaction;Synlett;2021-05-19

4. Selective Functionalization of Norbornadiene Through Nitrile Oxide Cycloaddition/Ring‐Opening/Cross‐Metathesis Protocols;Asian Journal of Organic Chemistry;2021-04-06

5. Diversity‐oriented Functionalization of Cyclodienes Through Selective Cycloaddition/Ring‐opening/Cross‐metathesis Protocols; Transformation of a “Flatland” into Three‐dimensional Scaffolds With Stereo‐ and Regiocontrol;The Chemical Record;2020-07-28

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