Applications of Allylsamarium Bromide as a Grignard Reagent and a Single-Electron Transfer Reagent in the One-Pot Synthesis of Dienes and Trienes

2010 ◽  
Vol 16 (5) ◽  
pp. 1697-1705 ◽  
Author(s):  
Yuanyuan Hu ◽  
Tao Zhao ◽  
Songlin Zhang
Keyword(s):  
Electron Transfer ◽  
Grignard Reagent ◽  
Single Electron ◽  
Single Electron Transfer ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One

Sulfonyl esters 6. Elucidation of the first sequence in the Trithioorthoformate Reaction

1995 ◽  
Vol 73 (3) ◽  
pp. 444-452 ◽  
Author(s):  
James Clayton Baum ◽  
Bradley Eugene Black ◽  
Laura Precedo ◽  
John Edward Goehl ◽  
Richard Francis Langler
Keyword(s):  
Electron Transfer ◽  
Single Electron ◽  
Single Electron Transfer ◽  
Computational Results ◽  
One Pot ◽  
The One ◽  
Sulfonate Ester

The one-pot conversion of a mercaptan and an aryl methanesulfonate into a trithioorthoformate is described. The intermediacy of a sulfide-sulfonate ester is firmly established. Experimental and computational results permit the formulation of a possible pathway for the formation of the intermediate sulfide-sulfonate ester. Keywords: single electron transfer, sulfonate esters, sulfide-sulfonate esters.

Sulfonyl esters 7. The second and third sequences in the Trithioorthoformate Reaction

1996 ◽  
Vol 74 (9) ◽  
pp. 1638-1648 ◽  
Author(s):  
Kashyapa Ananda Ginige ◽  
John Edward Goehl ◽  
Richard Francis Langler
Keyword(s):  
Electron Transfer ◽  
Key Words ◽  
Single Electron ◽  
Single Electron Transfer ◽  
One Pot ◽  
The One ◽  
Sulfonate Ester

A previous report has established the intermediacy of a sulfide-sulfonate ester in the one-pot conversion of an aryl mercaptan and a sulfonate ester into the corresponding trithioorthoformate. This report describes evidence for the sequential intermediacy of a bissulfide-sulfonate ester and a dithiosulfène in the conversion of the sulfide-sulfonate ester into the trithioorthoformate. A new sulfonate ester is shown to give the highest yield of trithioorthoformate. Key words: single electron transfer, sulfonate esters, sulfenes.

Applications of ytterbium(II) reagent as Grignard reagent and single electron transfer reagent in the synthesis of 3-substituted-2-oxindoles

Synthesis ◽  
2021 ◽  
Author(s):  
Pengkai Wang ◽  
yan xu cao ◽  
Songlin Zhang
Keyword(s):  
Electron Transfer ◽  
Grignard Reagent ◽  
Nucleophilic Reagent ◽  
Point Of View ◽  
Single Electron ◽  
Single Electron Transfer ◽  
One Pot ◽  
First Time ◽  
Isatin Derivatives

The utilities of ytterbium(II) reagent, both as nucleophilic reagent and single electron transfer reagent in the reaction of isatin derivatives with ytterbium(II) reagent are reported for the first time in this paper. From a synthetic point of view, a general, efficient, and experimentally simple one-pot method for preparation of 3-substituted-2-oxindoles was developed.

Reversal of Polarity by Catalytic SET Oxidation: Synthesis of Azabicyclo[m.n.o]alkanes via Chemoselective Reduction of Amidines

2021 ◽  
Author(s):  
Sundarababu Baskaran ◽  
Kirana D V ◽  
Kanak Kanti Das
Keyword(s):  
Electron Transfer ◽  
Stereoselective Synthesis ◽  
Single Electron ◽  
Single Electron Transfer ◽  
Catalytic Method ◽  
One Pot ◽  
Oxidative System ◽  
Oxidation Synthesis

A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this...

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