Electrostatic CH−π Interactions Can Override Fluorine <i>Gauche</i> Effects To Exert Conformational Control-Reference-Cited by-同舟云学术

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Electrostatic CH−π Interactions Can Override Fluorine Gauche Effects To Exert Conformational Control

Published:2022-12-05 Issue:6 Volume:29 Page:
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chemistry A European J

Author:

Emenike Bright U.¹^ORCID,Farshadmand Amiel¹,Zeller Matthias²,Roman Armando J.¹,Sevimler Arzu¹,Shinn David W.³

Affiliation:

1. Department of Chemistry & Physics State University of New York, Old Westbury 223 Store Hill Road Old Westbury NY 11568 USA

2. Department of Chemistry Purdue University West Lafayette IN 47907-2084 USA

3. Department of Mathematics and Science United States Merchant Marine Academy 300 Steamboat Road Kings Point NY 11024 USA

Funder

American Chemical Society Petroleum Research Fund

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202203139

Reference58 articles.

1. Informing Molecular Design by Stereoelectronic Theory: The Fluorine Gauche Effect in Catalysis

2. Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism

3. Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism

4.

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Conformational Analysis of 1,5-Diaryl-3-Oxo-1,4-Pentadiene Derivatives: A Nuclear Overhauser Effect Spectroscopy Investigation;International Journal of Molecular Sciences;2023-11-24

2. The Emergence and Properties of Selectively Fluorinated ‘Janus’ Cyclohexanes;The Chemical Record;2023-04-04

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