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Chiral N-Fmoc-β-Amino Alkyl Isonitriles Derived from Amino Acids: First Synthesis and Application in 1-Substituted Tetrazole Synthesis
A novel class of optically active N-Fmoc-protected amino isonitriles has been described for the first time. Conversion of the carboxyl group of Fmoc-β-amino acids into an isocyano group has resulted in a new class of N-urethane-protected amino isonitriles. All the isonitriles have been isolated as s...
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Published in: | Journal of organic chemistry 2009-01, Vol.74 (1), p.153-157 |
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container_title | Journal of organic chemistry |
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creator | Sureshbabu, Vommina V Narendra, N Nagendra, G |
description | A novel class of optically active N-Fmoc-protected amino isonitriles has been described for the first time. Conversion of the carboxyl group of Fmoc-β-amino acids into an isocyano group has resulted in a new class of N-urethane-protected amino isonitriles. All the isonitriles have been isolated as stable solids, purified, and completely characterized. A synthetic application of the obtained isonitriles has also been demonstrated through the synthesis of 1-substituted tetrazole analogues of amino acids via a 2 + 3 cycloaddition with trimethylsilyl azide. |
doi_str_mv | 10.1021/jo801527d |
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Org. Chem</addtitle><date>2009-01-02</date><risdate>2009</risdate><volume>74</volume><issue>1</issue><spage>153</spage><epage>157</epage><pages>153-157</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>A novel class of optically active N-Fmoc-protected amino isonitriles has been described for the first time. Conversion of the carboxyl group of Fmoc-β-amino acids into an isocyano group has resulted in a new class of N-urethane-protected amino isonitriles. All the isonitriles have been isolated as stable solids, purified, and completely characterized. A synthetic application of the obtained isonitriles has also been demonstrated through the synthesis of 1-substituted tetrazole analogues of amino acids via a 2 + 3 cycloaddition with trimethylsilyl azide.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>19055382</pmid><doi>10.1021/jo801527d</doi><tpages>5</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Amino Acids - chemistry Azides - chemistry Chemistry Cyclization Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings Molecular Conformation Nitriles - chemical synthesis Nitriles - chemistry Organic chemistry Preparations and properties Stereoisomerism Tetrazoles - chemistry Trimethylsilyl Compounds - chemistry |
title | Chiral N-Fmoc-β-Amino Alkyl Isonitriles Derived from Amino Acids: First Synthesis and Application in 1-Substituted Tetrazole Synthesis |
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