Theoretical Studies of Eliminations. 5. Intermolecular vs Intramolecular Eliminations: An ab Initio Study of the Gas-Phase Reaction of NH2 - with CH3CH2SCH3
Ab initio calculations at the MP2/6-31+G**//MP2/6-31+G* level have been completed on the title reaction. The computational results are in good accord with a mechanism suggested by Nibbering and co-workers in 1987. The preferred elimination pathway involves abstraction of an α-proton followed by an i...
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Veröffentlicht in: | Journal of organic chemistry 1996-12, Vol.61 (26), p.9430-9433 |
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container_title | Journal of organic chemistry |
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creator | Gronert, Scott Freed, Peter |
description | Ab initio calculations at the MP2/6-31+G**//MP2/6-31+G* level have been completed on the title reaction. The computational results are in good accord with a mechanism suggested by Nibbering and co-workers in 1987. The preferred elimination pathway involves abstraction of an α-proton followed by an intramolecular syn elimination. Although a conventional E2 mechanism is viable, abstraction of an α-proton has a substantial energetic advantage and is effectively irreversible. The intramolecular syn elimination has a higher barrier than a conventional anti E2 pathway, but is the only option after the irreversible α-proton abstraction. Results are also presented for the reaction of fluoride with CH3CH2SCH3. |
doi_str_mv | 10.1021/jo961482t |
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Intermolecular vs Intramolecular Eliminations: An ab Initio Study of the Gas-Phase Reaction of NH2 - with CH3CH2SCH3</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Ab initio calculations at the MP2/6-31+G**//MP2/6-31+G* level have been completed on the title reaction. The computational results are in good accord with a mechanism suggested by Nibbering and co-workers in 1987. The preferred elimination pathway involves abstraction of an α-proton followed by an intramolecular syn elimination. Although a conventional E2 mechanism is viable, abstraction of an α-proton has a substantial energetic advantage and is effectively irreversible. The intramolecular syn elimination has a higher barrier than a conventional anti E2 pathway, but is the only option after the irreversible α-proton abstraction. 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Intermolecular vs Intramolecular Eliminations: An ab Initio Study of the Gas-Phase Reaction of NH2 - with CH3CH2SCH3</title><author>Gronert, Scott ; Freed, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a136t-8decaa6ce7b807e19cd223d88e4a72668b19d87c3383fdba36fc83bf25fc84393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gronert, Scott</creatorcontrib><creatorcontrib>Freed, Peter</creatorcontrib><collection>Istex</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gronert, Scott</au><au>Freed, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Theoretical Studies of Eliminations. 5. Intermolecular vs Intramolecular Eliminations: An ab Initio Study of the Gas-Phase Reaction of NH2 - with CH3CH2SCH3</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>1996-12-27</date><risdate>1996</risdate><volume>61</volume><issue>26</issue><spage>9430</spage><epage>9433</epage><pages>9430-9433</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><abstract>Ab initio calculations at the MP2/6-31+G**//MP2/6-31+G* level have been completed on the title reaction. The computational results are in good accord with a mechanism suggested by Nibbering and co-workers in 1987. The preferred elimination pathway involves abstraction of an α-proton followed by an intramolecular syn elimination. Although a conventional E2 mechanism is viable, abstraction of an α-proton has a substantial energetic advantage and is effectively irreversible. The intramolecular syn elimination has a higher barrier than a conventional anti E2 pathway, but is the only option after the irreversible α-proton abstraction. Results are also presented for the reaction of fluoride with CH3CH2SCH3.</abstract><pub>American Chemical Society</pub><doi>10.1021/jo961482t</doi><tpages>4</tpages></addata></record> |
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title | Theoretical Studies of Eliminations. 5. Intermolecular vs Intramolecular Eliminations: An ab Initio Study of the Gas-Phase Reaction of NH2 - with CH3CH2SCH3 |
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