Trimethylsilylation of alcohols was achieved using 1,1,1,3,3,3-hexamethyldisilazane（HMDS） as silylating agent,in the presence of polyvinylpolypyrrolidonium tribromide in acetonitrile at room temperature.Also a varie...Trimethylsilylation of alcohols was achieved using 1,1,1,3,3,3-hexamethyldisilazane（HMDS） as silylating agent,in the presence of polyvinylpolypyrrolidonium tribromide in acetonitrile at room temperature.Also a variety of alcohols were converted into alkyl formates by ethyl formate and a catalytic amount of polyvinylpolypyrrolidonium tribromide under solvent free conditions at room temperature.展开更多
A highly efficient catalyst indium (III) tribromide is used to synthesize 5-alkoxy-carbonyl-4-hydrocarbyl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of beta-keto ester, aldehydes and urea through im...A highly efficient catalyst indium (III) tribromide is used to synthesize 5-alkoxy-carbonyl-4-hydrocarbyl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of beta-keto ester, aldehydes and urea through improved Biginelli reaction.展开更多
An efficient synthetic method for bis（indol-3-yl）alkane derivatives has been developed.In the presence of 5 mol%of pyridinium tribromide（PTB）,the condensation of indoles and aldehydes proceeded smoothly under mild...An efficient synthetic method for bis（indol-3-yl）alkane derivatives has been developed.In the presence of 5 mol%of pyridinium tribromide（PTB）,the condensation of indoles and aldehydes proceeded smoothly under mild conditions,giving rise to the corresponding bis（indol-3-yl）alkanes in good to excellent yields.展开更多
Poly（4-vinylpyridinium tribromide） was prepared from poly（4-vinylpyridin） and used for the selective oxidation of a variety of sulfides to the corresponding sulfoxides. The oxidation reaction was carried out heter...Poly（4-vinylpyridinium tribromide） was prepared from poly（4-vinylpyridin） and used for the selective oxidation of a variety of sulfides to the corresponding sulfoxides. The oxidation reaction was carried out heterogeneously in acetone/water, as green solvent, at room temperature.展开更多
Pentylpyridinium tribromide and aqueous ammonium acetate was used for the rapid oxidative conversion of benzyl alcohols, benzaldehydes and benzyl amines to the corresponding benzonitriles in good to excellent yields. ...Pentylpyridinium tribromide and aqueous ammonium acetate was used for the rapid oxidative conversion of benzyl alcohols, benzaldehydes and benzyl amines to the corresponding benzonitriles in good to excellent yields. This simple, mild and one-pot system provides easy workup and separation of the products.展开更多
{[K.18-Crown-6]Br3}n,a unique tribromide-type catalyst,was utilized for the N-boc protection of amines and trimethylsilylation(TMS)and tetrahydropyranylation(THP)of alcohols.The method is general for the preparation o...{[K.18-Crown-6]Br3}n,a unique tribromide-type catalyst,was utilized for the N-boc protection of amines and trimethylsilylation(TMS)and tetrahydropyranylation(THP)of alcohols.The method is general for the preparation of N-boc derivatives of aliphatic(acyclic and cyclic)and aromatic,and primary and secondary amines and also various TMS-ethers and THP-ethers.The simple separation of the catalyst from the product is one of the many advantages of this method.展开更多
A mild and efficient method for the conversion of alcohols to their corresponding methoxymethyl ethers and acetates using benzyltriphenylphosphonium tribromide （BTPTB） as catalyst is described. All reactions were pe...A mild and efficient method for the conversion of alcohols to their corresponding methoxymethyl ethers and acetates using benzyltriphenylphosphonium tribromide （BTPTB） as catalyst is described. All reactions were performed under completely heterogeneous reaction conditions in good to high yields.展开更多
Early in the 1980 s, Meyer dissolved appropriate amounts of CsCl and PrCl<sub>3</sub>·7H<sub>2</sub>O ina small amount of concentrated hydrochloric acid for getting CsPr<sub>2</su...Early in the 1980 s, Meyer dissolved appropriate amounts of CsCl and PrCl<sub>3</sub>·7H<sub>2</sub>O ina small amount of concentrated hydrochloric acid for getting CsPr<sub>2</sub>Cl<sub>7</sub>（hyd.）, and then thesample CsPr<sub>2</sub>Cl<sub>7</sub>（hyd.）was dehydrated by heating in HCl stream at high temperature. Thereaction equation is as follows:展开更多
This paper presents a versatile reagent for epoxide cleavage.The allyltin tribromide could act as a novel and easily prepared allylation reagent and halide atom donor to convert epoxides to the corresponding homoallyl...This paper presents a versatile reagent for epoxide cleavage.The allyltin tribromide could act as a novel and easily prepared allylation reagent and halide atom donor to convert epoxides to the corresponding homoallyl alcohols and halohydrins in high yields with excellent regioselectivities under mild reaction conditions,respectively.It could also act as a Lewis acid to catalyze the ring opening reactions of epoxides with alcohols.展开更多
It was found that, when the Baylis-Hillman reaction of arylaldehydes withmethyl vinyl ketone was carried out at below - 20℃ in the presence of boron (Ⅲ) tribromide ortitanium (Ⅳ) bromide using a catalytic amount of...It was found that, when the Baylis-Hillman reaction of arylaldehydes withmethyl vinyl ketone was carried out at below - 20℃ in the presence of boron (Ⅲ) tribromide ortitanium (Ⅳ) bromide using a catalytic amount of Lewis base such as amine, the brominated compoundsand the Baylis-Hillman adducts could be obtained as the major products in good yields for variousaryl aldehydes. But at room temperature, the elimination products were the major products. Inaddition, the palladium catalyzed allylic substitution reactions of the e-limination products werealso examined.展开更多
Poly(4-vinylpyridinium tribromide) is an efficient catalyst for the conversion of various alcohols to their corresponding acetate derivatives with acetic anhydride.This method has some advantages such as mild reaction...Poly(4-vinylpyridinium tribromide) is an efficient catalyst for the conversion of various alcohols to their corresponding acetate derivatives with acetic anhydride.This method has some advantages such as mild reaction conditions,good to excellent yields,and ease of work-up.展开更多
An efficient procedure for the trimethylsilylation of alcohols and phenols is presented.The combination of 1,1,1,3,3,3-hexamethyldisilazane and a catalytic amount of phenyltrimethylammonium tribromide(PhMe3N+Br3?) was...An efficient procedure for the trimethylsilylation of alcohols and phenols is presented.The combination of 1,1,1,3,3,3-hexamethyldisilazane and a catalytic amount of phenyltrimethylammonium tribromide(PhMe3N+Br3?) was found to be effective for the trimethylsilylation of alcohols and phenols.The protection reaction is very simple and homogenously performed in dichloromethane at room temperature and mild conditions.展开更多
The reductive deoxygenation of aldehydes and ketones into the corresponding alkanes is accomplished by LiAlH4, in the presence of Lewis acid InBr3. It provides a convenient method to complete the transformation from c...The reductive deoxygenation of aldehydes and ketones into the corresponding alkanes is accomplished by LiAlH4, in the presence of Lewis acid InBr3. It provides a convenient method to complete the transformation from carbonyl compounds to alkanes.展开更多
文摘Trimethylsilylation of alcohols was achieved using 1,1,1,3,3,3-hexamethyldisilazane（HMDS） as silylating agent,in the presence of polyvinylpolypyrrolidonium tribromide in acetonitrile at room temperature.Also a variety of alcohols were converted into alkyl formates by ethyl formate and a catalytic amount of polyvinylpolypyrrolidonium tribromide under solvent free conditions at room temperature.
基金the National Natural Science Foundation of China(29872018&29972026).
文摘A highly efficient catalyst indium (III) tribromide is used to synthesize 5-alkoxy-carbonyl-4-hydrocarbyl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of beta-keto ester, aldehydes and urea through improved Biginelli reaction.
基金the National Natural Science Foundation of China(Nos.20862009 and 20962010)the National Natural Science Foundation of Jiangxi Province(No.2008GQH0026)the Science Foundation of Education Department of Jiangxi Province(No.GJJ10386) for their financial support
文摘An efficient synthetic method for bis（indol-3-yl）alkane derivatives has been developed.In the presence of 5 mol%of pyridinium tribromide（PTB）,the condensation of indoles and aldehydes proceeded smoothly under mild conditions,giving rise to the corresponding bis（indol-3-yl）alkanes in good to excellent yields.
基金Financial support for this work by the Ilam University,Ilam,Iran is gratefully acknowledged
文摘Poly（4-vinylpyridinium tribromide） was prepared from poly（4-vinylpyridin） and used for the selective oxidation of a variety of sulfides to the corresponding sulfoxides. The oxidation reaction was carried out heterogeneously in acetone/water, as green solvent, at room temperature.
文摘Pentylpyridinium tribromide and aqueous ammonium acetate was used for the rapid oxidative conversion of benzyl alcohols, benzaldehydes and benzyl amines to the corresponding benzonitriles in good to excellent yields. This simple, mild and one-pot system provides easy workup and separation of the products.
基金support for this work from the research affairs of Hamedan University of Medical Sciences,Hamedan,I.R.Iranpartial support of this work by the Research Affairs Office of Bu-Ali Sina UniversityCenter of Excellence in Development of Chemical Method(CEDCM)Hamedan,I.R.Iran
文摘{[K.18-Crown-6]Br3}n,a unique tribromide-type catalyst,was utilized for the N-boc protection of amines and trimethylsilylation(TMS)and tetrahydropyranylation(THP)of alcohols.The method is general for the preparation of N-boc derivatives of aliphatic(acyclic and cyclic)and aromatic,and primary and secondary amines and also various TMS-ethers and THP-ethers.The simple separation of the catalyst from the product is one of the many advantages of this method.
文摘A mild and efficient method for the conversion of alcohols to their corresponding methoxymethyl ethers and acetates using benzyltriphenylphosphonium tribromide （BTPTB） as catalyst is described. All reactions were performed under completely heterogeneous reaction conditions in good to high yields.
基金Project supported by the National Natural Science Foundation of China.
文摘Early in the 1980 s, Meyer dissolved appropriate amounts of CsCl and PrCl<sub>3</sub>·7H<sub>2</sub>O ina small amount of concentrated hydrochloric acid for getting CsPr<sub>2</sub>Cl<sub>7</sub>（hyd.）, and then thesample CsPr<sub>2</sub>Cl<sub>7</sub>（hyd.）was dehydrated by heating in HCl stream at high temperature. Thereaction equation is as follows:
文摘This paper presents a versatile reagent for epoxide cleavage.The allyltin tribromide could act as a novel and easily prepared allylation reagent and halide atom donor to convert epoxides to the corresponding homoallyl alcohols and halohydrins in high yields with excellent regioselectivities under mild reaction conditions,respectively.It could also act as a Lewis acid to catalyze the ring opening reactions of epoxides with alcohols.
文摘It was found that, when the Baylis-Hillman reaction of arylaldehydes withmethyl vinyl ketone was carried out at below - 20℃ in the presence of boron (Ⅲ) tribromide ortitanium (Ⅳ) bromide using a catalytic amount of Lewis base such as amine, the brominated compoundsand the Baylis-Hillman adducts could be obtained as the major products in good yields for variousaryl aldehydes. But at room temperature, the elimination products were the major products. Inaddition, the palladium catalyzed allylic substitution reactions of the e-limination products werealso examined.
基金supported by the Research Facilities of Ilam University,Iran
文摘Poly(4-vinylpyridinium tribromide) is an efficient catalyst for the conversion of various alcohols to their corresponding acetate derivatives with acetic anhydride.This method has some advantages such as mild reaction conditions,good to excellent yields,and ease of work-up.
基金Supported by the research faculties of Ilam University,Ilam,Iran
文摘An efficient procedure for the trimethylsilylation of alcohols and phenols is presented.The combination of 1,1,1,3,3,3-hexamethyldisilazane and a catalytic amount of phenyltrimethylammonium tribromide(PhMe3N+Br3?) was found to be effective for the trimethylsilylation of alcohols and phenols.The protection reaction is very simple and homogenously performed in dichloromethane at room temperature and mild conditions.
基金the National Natural Science Foundation of China(29872018&29972026)the Key Laboratory of Elemento-oiganic Cheraistiy,Nankai University and RFDP,China's Ministry of Higher Education(1999005520)for their financial support
文摘The reductive deoxygenation of aldehydes and ketones into the corresponding alkanes is accomplished by LiAlH4, in the presence of Lewis acid InBr3. It provides a convenient method to complete the transformation from carbonyl compounds to alkanes.
