Transesterification of alkyl carbamate to aryl carbamate : Effect of varying the alkyl group

DOI: 10.1016/S0040-4020(01)81769-5

Source and publish data:

Tetrahedron p. 10367 - 10370 (1994)

Update date:2022-08-28

Topics:

Authors:

Deshpande, Sunita R.

Likhite, Anjali P.

Rajappa, Srinivasachari

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4020(01)81769-5

Phosphorus oxychloride mediated transesterification of four alkyl N-methylcarbamates to several aryl N-methylcarbamates has been studied. Best yields are obtained from benzyl N-methylcarbamate.

Full text of DOI:10.1016/S0040-4020(01)81769-5

Products guided by the article

Product name:propan-2-yl N-methylcarbamate

Cas No:10047-90-2

R&D Labs maybe for 10047-90-2

Jining tiansheng chemical co.,ltd.

Contact:+86-537-5158722

Address:ROOM 1011, BLOCK B, CUIDU INTERNATIOAL BUSINESS CENTER, JINING CITY, CHINA
Tianjin Ingenochem Technology Co.,Ltd

Contact:+86-22-23677060

Address:Hitech Green Industry Park K2-9-602, Nankai district
Hubei Xinjing New Material Co.,Ltd

Contact:+86-27-83313147

Address:Room402.#Bthe 7th,Headquarter of Huifeng Corporation Qiaokou District,Wuhan China
Luna Chemicals Co.,Ltd.

Contact:+86-570-4336358

Address:No.87 Building,Tianqian,Sidu Town
ZCIC INTERNATIONAL LTD

Contact:+86-512-56795332

Address:No227 Shuanglong Rd, Fenghuang, Zhangjiagang

Relevant to this article

Michael addition of nitromethane to non-racemic chiral Cr(CO)₃ complexes of ethyl cinnamate derivatives: Stereoselective synthesis of (R)-(-)-baclofen

Doi:10.1016/S0957-4166(00)00123-3
(2000)
Synthesis of mixed carbonates via a three-component coupling of alcohols, CO₂, and alkyl halides in the presence of K₂CO₃ and tetrabutylammonium iodide

Doi:10.3390/70400386
(2002)
Pulsed EPR study of amino acid and tetrahydropterin binding in a tyrosine hydroxylase nitric oxide complex: Evidence for substrate rearrangements in the formation of the oxygen-reactive complex

Doi:10.1021/bi4010914
(2013)
Microwave-Assisted and L-proline catalysed domino cyclisation in an aqueous medium: A rapid, highly efficient and green synthesis of benzo[a]phenazine annulated heterocycles

Doi:10.3184/174751916X14787124908891
(2016)
Nanocomposites based on borate esters as improved lithium-ion electrolytes

Doi:10.1039/c1jm11189b
(2011)
Doi:10.1039/jr9530000342
(1953)

Article Doi

Transesterification of alkyl carbamate to aryl carbamate : Effect of varying the alkyl group

DOI: 10.1016/S0040-4020(01)81769-5

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(01)81769-5

Full text of DOI:10.1016/S0040-4020(01)81769-5

Products guided by the article

R&D Labs maybe for 10047-90-2

Relevant to this article

Michael addition of nitromethane to non-racemic chiral Cr(CO)3 complexes of ethyl cinnamate derivatives: Stereoselective synthesis of (R)-(-)-baclofen

Synthesis of mixed carbonates via a three-component coupling of alcohols, CO2, and alkyl halides in the presence of K2CO3 and tetrabutylammonium iodide

Pulsed EPR study of amino acid and tetrahydropterin binding in a tyrosine hydroxylase nitric oxide complex: Evidence for substrate rearrangements in the formation of the oxygen-reactive complex

Microwave-Assisted and L-proline catalysed domino cyclisation in an aqueous medium: A rapid, highly efficient and green synthesis of benzo[a]phenazine annulated heterocycles

Nanocomposites based on borate esters as improved lithium-ion electrolytes

Michael addition of nitromethane to non-racemic chiral Cr(CO)₃ complexes of ethyl cinnamate derivatives: Stereoselective synthesis of (R)-(-)-baclofen

Synthesis of mixed carbonates via a three-component coupling of alcohols, CO₂, and alkyl halides in the presence of K₂CO₃ and tetrabutylammonium iodide