Benzyl Acetylcarbamate Potassium Salt (BENAC-K): A Simple Nucleophilic N-Acetamide Equivalent
Abstract Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected N -alkylacetamides in high yields by simple treatment with an almost equimolar (1.1 equiv) amoun...
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Veröffentlicht in: | Synthesis (Stuttgart) 2019-10, Vol.51 (19), p.3638-3650 |
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container_title | Synthesis (Stuttgart) |
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creator | Sakai, Takeo Tatematsu, Toshiki Fukuta, Ayumi Kasai, Satomi Hayashi, Kahori Mori, Yuji |
description | Abstract
Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected
N
-alkylacetamides in high yields by simple treatment with an almost equimolar (1.1 equiv) amount of BENAC-K in a polar solvent. |
doi_str_mv | 10.1055/s-0039-1690097 |
format | Article |
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Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected
N
-alkylacetamides in high yields by simple treatment with an almost equimolar (1.1 equiv) amount of BENAC-K in a polar solvent.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0039-1690097</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><ispartof>Synthesis (Stuttgart), 2019-10, Vol.51 (19), p.3638-3650</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-ceb57bea2601dac540b11ae7f8ffb439f5d682c3d13a0903b07af358868d1ae33</citedby><orcidid>0000-0002-9006-8249</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0039-1690097.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0039-1690097$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>315,781,785,3018,3019,27929,27930,54564,54565</link.rule.ids></links><search><creatorcontrib>Sakai, Takeo</creatorcontrib><creatorcontrib>Tatematsu, Toshiki</creatorcontrib><creatorcontrib>Fukuta, Ayumi</creatorcontrib><creatorcontrib>Kasai, Satomi</creatorcontrib><creatorcontrib>Hayashi, Kahori</creatorcontrib><creatorcontrib>Mori, Yuji</creatorcontrib><title>Benzyl Acetylcarbamate Potassium Salt (BENAC-K): A Simple Nucleophilic N-Acetamide Equivalent</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract
Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected
N
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Benzyl acetylcarbamate potassium salt (BENAC-K) has been developed as a simple nucleophilic acetamide equivalent. A broad variety of alkyl halides were converted into benzyloxycarbonyl-protected
N
-alkylacetamides in high yields by simple treatment with an almost equimolar (1.1 equiv) amount of BENAC-K in a polar solvent.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0039-1690097</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-9006-8249</orcidid></addata></record> |
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title | Benzyl Acetylcarbamate Potassium Salt (BENAC-K): A Simple Nucleophilic N-Acetamide Equivalent |
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