Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination
An rapid and efficient microwave assisted Pd(II) catalyzed protocol for the preparation of N-methyl-6-heterocyclic-1-oxoisoindoline derivatives by Buchwald-Hartwig amination with an overall yield 68-85% has been described.
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Wiley
2011-01-01
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| Series: | E-Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2011/851935 |
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| _version_ | 1832560080020570112 |
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| author | C. Kishor Kumar H. Vijay Kumar Nagaraja Naik |
| author_facet | C. Kishor Kumar H. Vijay Kumar Nagaraja Naik |
| author_sort | C. Kishor Kumar |
| collection | DOAJ |
| description | An rapid and efficient microwave assisted Pd(II) catalyzed protocol for the preparation of N-methyl-6-heterocyclic-1-oxoisoindoline derivatives by Buchwald-Hartwig amination with an overall yield 68-85% has been described. |
| format | Article |
| id | doaj-art-f7a29c509cc64df185a6ba223c876946 |
| institution | Kabale University |
| issn | 0973-4945 2090-9810 |
| language | English |
| publishDate | 2011-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | E-Journal of Chemistry |
| spelling | doaj-art-f7a29c509cc64df185a6ba223c8769462025-02-03T01:28:36ZengWileyE-Journal of Chemistry0973-49452090-98102011-01-01831108111310.1155/2011/851935Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig AminationC. Kishor Kumar0H. Vijay Kumar1Nagaraja Naik2Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore-570 006, Karnataka, IndiaDepartment of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore-570 006, Karnataka, IndiaDepartment of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore-570 006, Karnataka, IndiaAn rapid and efficient microwave assisted Pd(II) catalyzed protocol for the preparation of N-methyl-6-heterocyclic-1-oxoisoindoline derivatives by Buchwald-Hartwig amination with an overall yield 68-85% has been described.http://dx.doi.org/10.1155/2011/851935 |
| spellingShingle | C. Kishor Kumar H. Vijay Kumar Nagaraja Naik Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination E-Journal of Chemistry |
| title | Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination |
| title_full | Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination |
| title_fullStr | Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination |
| title_full_unstemmed | Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination |
| title_short | Synthesis of N-Methyl-6-heterocyclic-1-oxoisoindoline Derivatives by Microwave Assisted Buchwald-Hartwig Amination |
| title_sort | synthesis of n methyl 6 heterocyclic 1 oxoisoindoline derivatives by microwave assisted buchwald hartwig amination |
| url | http://dx.doi.org/10.1155/2011/851935 |
| work_keys_str_mv | AT ckishorkumar synthesisofnmethyl6heterocyclic1oxoisoindolinederivativesbymicrowaveassistedbuchwaldhartwigamination AT hvijaykumar synthesisofnmethyl6heterocyclic1oxoisoindolinederivativesbymicrowaveassistedbuchwaldhartwigamination AT nagarajanaik synthesisofnmethyl6heterocyclic1oxoisoindolinederivativesbymicrowaveassistedbuchwaldhartwigamination |