Iodine-catalyzed regioselective 2-sulfonylation of indoles with sodium sulfinates

F **ao, H Chen, H **e, S Chen, L Yang, GJ Deng - Organic letters, 2014 - ACS Publications
Iodine-Catalyzed Regioselective 2-Sulfonylation of Indoles with Sodium Sulfinates | Organic
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Pd-catalyzed desulfitative heck coupling with dioxygen as the terminal oxidant

X Zhou, J Luo, J Liu, S Peng, GJ Deng - Organic Letters, 2011 - ACS Publications
A Pd-catalyzed desulfitative Heck-type reaction of aromatic sulfinic acid sodium salts with
various olefins is developed with O2 as the terminal oxidant under mild conditions. The …

Palladium‐Catalyzed Desulfitative C H Arylation of Heteroarenes with Sodium Sulfinates

B Liu, Q Guo, Y Cheng, J Lan, J You - Chemistry–A European Journal, 2011 - infona.pl
Palladium‐Catalyzed Desulfitative CH Arylation of Heteroarenes with Sodium Sulfinates ×
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Direct Synthesis of Aryl Ketones by Palladium‐Catalyzed Desulfinative Addition of Sodium Sulfinates to Nitriles

J Liu, X Zhou, H Rao, F **ao, CJ Li, GJ Deng - Chemistry–A European …, 2011 - infona.pl
Mild yet direct: A convenient and efficient method for the synthesis of various aryl ketones by
palladium‐catalyzed desulfinative addition of aromatic sulfinic acid sodium salts to various …

A highly efficient palladium-catalyzed desulfitative arylation of azoles with sodium arylsulfinates

M Wang, D Li, W Zhou, L Wang - Tetrahedron, 2012 - Elsevier
A highly efficient palladium-catalyzed direct desulfitative arylation of azoles at C2-position
has been developed using sodium arylsulfinates as aryl sources. Azoles including …

Extraordinary difference in reactivity of ozone (OOO) and sulfur dioxide (OSO): a theoretical study

Y Lan, SE Wheeler, KN Houk - Journal of Chemical Theory and …, 2011 - ACS Publications
Ozone and sulfur dioxide are valence isoelectronic yet show very different reactivity. While
ozone is one of the most reactive 1, 3-dipoles, SO2 does not react in this way at all. The …

Ruthenium(IV)‐Catalyzed Isomerization of the CC Bond of O‐Allylic Substrates: A Theoretical and Experimental Study

A Varela‐Álvarez, JA Sordo, E Piedra… - … A European Journal, 2011 - Wiley Online Library
A general mechanism to rationalize RuIV‐catalyzed isomerization of the C C bond in O‐
allylic substrates is proposed. Calculations supporting the proposed mechanism were …

An efficient tandem elimination–cyclization–desulfitative arylation of 2-(gem-dibromovinyl) phenols (thiophenols) with sodium arylsulfinates

W Chen, P Li, T Miao, LG Meng, L Wang - Organic & Biomolecular …, 2013 - pubs.rsc.org
An efficient tandem elimination–cyclization–desulfitative arylation of 2-(gem-dibromovinyl)
phenols (thiophenols) with sodium arylsulfinates has been developed. In the presence of …

Palladium-catalyzed desulfitative addition of sodium sulfinates with α, β-unsaturated carbonyl compounds

W Chen, X Zhou, F **ao, J Luo, GJ Deng - Tetrahedron Letters, 2012 - Elsevier
Palladium-catalyzed desulfitative addition of sodium sulfinates with α,β-unsaturated
carbonyl compounds - ScienceDirect Skip to main contentSkip to article Elsevier logo …

Amides in one pot from carboxylic acids and amines via sulfinylamides

J Bai, BK Zambron, P Vogel - Organic letters, 2014 - ACS Publications
An efficient method has been developed for the direct amidification of carboxylic acids via
sulfinylamides preformed in situ by the reaction of pure amines with prop-2-ene-1-sulfinyl …