Stereoelectronic effects in conformations of sulfide, sulfoxide, and sulfone α-carbanions
Author:
Funder
Deutsche Forschungsgemeinschaft
Konrad-Adenauer-Stiftung
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference78 articles.
1. Sulfur Reagents in Organic Synthesis;Metzner,1994
2. Organosulfur chemistry. II. Highly stereoselective reactions of 1,3-dithianes. Contrathermodynamic formation of unstable diastereoisomers
3. Organosulfur chemistry. 3. NMR spectra of carbanions derived from 1,3-dithianes as related to the high stereoselectivity in their reactions with electrophiles
4. Stereoelectronic effects in the gas-phase. 2. Negative ion reactions of 1,3-dithianes and 1,3-dithiane 1-oxides
5. A Density Functional Study of 2-Lithio-1,3-dithiane and 2-Lithio-2-phenyl-1,3-dithiane: Conformational Preference of the C−Li Bond and Structural Analysis
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2. Development of a Robust Protocol for the Determination of Weak Acids’ pKa Values in DMSO;The Journal of Organic Chemistry;2020-07-17
3. Stereoelectronic Effects: Perlin Effects in Thiane‐Derived Compounds;European Journal of Organic Chemistry;2020-04-07
4. Stereoelectronic Effects: The γ-Gauche Effect in Sulfoxides;The Journal of Physical Chemistry A;2018-06-12
5. 1H, 13C NMR and ESI–MS studies of 1:1 complexes of some sulfenyl carbon acids with 1,5,7-triazabicyclo[4.4.0]dec-5-ene in solution;International Journal of Mass Spectrometry;2016-12
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