Synthesis of Novel 2,6-Diazaspiro[3.3]heptanes
Abstract A practical route to 2,6-diazaspiro[3.3]heptanes is described by way of reductive amination of a readily available aldehyde with primary amines or anilines. Cyclisation proceeds in high yield and the methods reported are amenable to either library or large-scale synthesis.
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Veröffentlicht in: | Synlett 2007-10, Vol.2007 (16), p.2584-2586 |
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container_issue | 16 |
container_start_page | 2584 |
container_title | Synlett |
container_volume | 2007 |
creator | Hamza, Daniel Stocks, Michael J. Décor, Anne Pairaudeau, Garry Stonehouse, Jeffrey P. |
description | Abstract
A practical route to 2,6-diazaspiro[3.3]heptanes is described by way of reductive amination of a readily available aldehyde with primary amines or anilines. Cyclisation proceeds in high yield and the methods reported are amenable to either library or large-scale synthesis. |
doi_str_mv | 10.1055/s-2007-986650 |
format | Article |
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A practical route to 2,6-diazaspiro[3.3]heptanes is described by way of reductive amination of a readily available aldehyde with primary amines or anilines. Cyclisation proceeds in high yield and the methods reported are amenable to either library or large-scale synthesis.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp1j01Lw0AURQdRMFaX7vMDOvFN5jNLqVqFogt1JTJMJm9ISpuETBTqrzclbl09uBzufYeQawYZAylvIs0BNC2MUhJOSMIE11NUqFOSQMEVlTkT5-Qixi0AE6aAhGSvh3asMTYx7UL63H3jLs2Xit417sfFvhm6D57xzxr70bUYL8lZcLuIV393Qd4f7t9Wj3Tzsn5a3W6oz7UYqQEEUJURCEYKX5ZcIkPDdfBcQxDTegiF1t6VlRZCBsVKVfrKi5BzKQ1fEDr3-qGLccBg-6HZu-FgGdijrI32KGtn2YlfzvxYN7hHu-2-hnZ68B_8F5y_U3o</recordid><startdate>20071001</startdate><enddate>20071001</enddate><creator>Hamza, Daniel</creator><creator>Stocks, Michael J.</creator><creator>Décor, Anne</creator><creator>Pairaudeau, Garry</creator><creator>Stonehouse, Jeffrey P.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20071001</creationdate><title>Synthesis of Novel 2,6-Diazaspiro[3.3]heptanes</title><author>Hamza, Daniel ; Stocks, Michael J. ; Décor, Anne ; Pairaudeau, Garry ; Stonehouse, Jeffrey P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-80e006d84e0854cbb35e1e837fc370f4014ff977cabd7445f61b6bcdc4f235583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hamza, Daniel</creatorcontrib><creatorcontrib>Stocks, Michael J.</creatorcontrib><creatorcontrib>Décor, Anne</creatorcontrib><creatorcontrib>Pairaudeau, Garry</creatorcontrib><creatorcontrib>Stonehouse, Jeffrey P.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hamza, Daniel</au><au>Stocks, Michael J.</au><au>Décor, Anne</au><au>Pairaudeau, Garry</au><au>Stonehouse, Jeffrey P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Novel 2,6-Diazaspiro[3.3]heptanes</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2007-10-01</date><risdate>2007</risdate><volume>2007</volume><issue>16</issue><spage>2584</spage><epage>2586</epage><pages>2584-2586</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
A practical route to 2,6-diazaspiro[3.3]heptanes is described by way of reductive amination of a readily available aldehyde with primary amines or anilines. Cyclisation proceeds in high yield and the methods reported are amenable to either library or large-scale synthesis.</abstract><doi>10.1055/s-2007-986650</doi><tpages>3</tpages></addata></record> |
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language | eng |
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source | Thieme Connect Journals |
subjects | letter |
title | Synthesis of Novel 2,6-Diazaspiro[3.3]heptanes |
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