|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
10
|
|
pubmed:dateCreated |
2011-5-13
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|
pubmed:abstractText |
A convenient, general, and high yielding Pd-catalyzed cross-coupling of methanesulfonamide with aryl bromides and chlorides is reported. The use of this method eliminates concern over genotoxic impurities that can arise when an aniline is reacted with methanesulfonyl chloride. The application of this method to the synthesis of dofetilide is also reported.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
May
|
|
pubmed:issn |
1523-7052
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|
pubmed:author |
|
|
pubmed:issnType |
Electronic
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|
pubmed:day |
20
|
|
pubmed:volume |
13
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
2564-7
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|
pubmed:meshHeading |
|
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pubmed:year |
2011
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|
pubmed:articleTitle |
Mild Pd-catalyzed N-arylation of methanesulfonamide and related nucleophiles: avoiding potentially genotoxic reagents and byproducts.
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|
pubmed:affiliation |
Eli Lilly and Company, Lilly Corporate Center, Indianapolis, Indiana 46285, United States.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
