The Experts below are selected from a list of 4623 Experts worldwide ranked by ideXlab platform
Xuhong Qian - One of the best experts on this subject based on the ideXlab platform.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives.
The Journal of organic chemistry, 2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives
2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products
Yian Feng - One of the best experts on this subject based on the ideXlab platform.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives.
The Journal of organic chemistry, 2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives
2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products
Minming Zou - One of the best experts on this subject based on the ideXlab platform.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives.
The Journal of organic chemistry, 2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives
2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products
Runjiang Song - One of the best experts on this subject based on the ideXlab platform.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives.
The Journal of organic chemistry, 2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives
2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products
Xusheng Shao - One of the best experts on this subject based on the ideXlab platform.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives.
The Journal of organic chemistry, 2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products.
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Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives
2016Co-Authors: Yian Feng, Minming Zou, Runjiang Song, Xusheng Shao, Xuhong QianAbstract:A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The Solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aProtic Solvent chloroform, while in the Protic Solvent ethanol, 1,3-thiazetidines were the main products
