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DOI: 10.1055/s-2007-968003
Sodium Azide (NaN3): A Versatile Reagent in Organic Synthesis
Publikationsverlauf
Publikationsdatum:
07. Februar 2007 (online)

Introduction
Sodium azide is a colorless, odorless, white crystalline solid, which is commercially available and widely used in industry, agriculture, medical practice, and organic transformations. It has been used for synthesis of β- and γ-azidoarylketones, [1] dialkylcarbamoyl azides, [2] diphenylphosphoryl azides, [3] acyl azides, [4] aryl azides, [5] allyl azides, [6] 1,5-fused tetrazoles, [7] 5-substituted 1H-tetrazoles, [8] 1,2,3-triazoles, [9] 1-aryl 1,2,3-triazoles, [10] 1,4-disubstituted 1,2,3-triazoles, [11] and 1-N-glycosylthiomethyl-1,2,3-triazoles. [12] In addition, sodium azide has been widely employed for preparation of α-azidoketones, [13] 1-aryl-1H-benzotriazoles, [14] 3-cyanoindoles, [15] and Fmoc-protected amino alcohols, [16] as a suitable nucleophile for the Michael-induced ring closure of 2-bromoalkylidenemalonates to 3,3-dialkyl-2-azidocyclopropane-1,1-dicarboxylates. [17]
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Singh PND.Muthukrishnan S.Murthy RS.Klima RF.Mandel SM.Hawk M.Yarbrough N.Gudmundsdóttie AD. Tetrahedron Lett. 2003, 44: 9169 - 2
Gumaste VK.Deshmukh ARAS. Tetrahedron Lett. 2004, 45: 6571 - 3
Wolff O.Waldvogel SR. Synthesis 2005, 1303 -
4a
Sridhar R.Perumal PT. Synth. Commun. 2003, 33: 607 -
4b
Bose DS.Reddy AVN. Tetrahedron Lett. 2003, 44: 3543 -
4d
Bao W.Wang Q. J. Chem. Res., Synop. 2003, 700 -
5a
Andersen J.Madsen U.Björkling F.Liang X. Synlett 2005, 2209 -
5b
Zhu W.Ma D.-W. Chem. Commun. 2004, 888 -
5c
Das J.Patil SN.Awasthi R.Narasimhulu CP.Trehan S. Synthesis 2005, 1801 - 6
Jayanthi A.Gumaste VK.Deshmukh ARAS. Synlett 2004, 979 - 7
Eshghi H.Hassankhani A. Synth. Commun. 2005, 35: 1115 -
8a
Kantam ML.Kumar KBS.Sridhar Ch. Adv. Synth. Catal. 2005, 347: 1212 -
8b
Kantam ML.Kumar KBS.Raja KP. J. Mol. Catal. A: Chem. 2006, 247: 186 -
9a
Quiclet-Sire B.Zard SZ. Synthesis 2005, 3319 -
9b
Kacprzak K. Synlett 2005, 943 -
9c
Appukkuttan P.Dehaen W.Fokin VV.Van der Eycken E. Org. Lett. 2004, 6: 4223 - 10
Andersen J.Bolvig S.Liang X. Synlett 2005, 2941 - 11
Zhao Y.-B.Yan Z.-Y.Liang Y.-M. Tetrahedron Lett. 2006, 47: 1545 - 12
Zhu X.-M.Schmidt RB. J. Org Chem. 2004, 69: 1081 - 13
Kumar D.Sundaree S.Rao VS. Synth. Commun. 2006, 36: 1893 - 14
Chen Z.-Y.Wu M.-J. Org. Lett. 2005, 7: 475 - 15
Jaisankar P.Srinivasan PC. Synthesis 2006, 2413 - 16
Mondal S.Fan E. Synlett 2006, 306 - 17
Mangelinckx S.De Kimpe N. Synlett 2006, 369 -
18a
Sreedhar B.Reddy PS.Kunar NS. Tetrahedron Lett. 2006, 47: 3055 -
18b
Chandrasekhar S.Basu D.Rambabu Ch. Tetrahedron Lett. 2006, 47: 3059 - 19
Lebel H.Leogane O. Org. Lett. 2005, 7: 4107 - 20
Su W.-K.Hong Z.Shan W.-G.Zhang X.-X. Eur. J. Org. Chem. 2006, 2723 - 21
Yadav JS.Reddy BVS.Sadashiv K.Raghavendra S.Harikishan K. Catal. Commun. 2004, 5: 111 -
22a
Kazemi F.Kiasat AR.Ebrahimi S. Synth. Commun. 2003, 33: 999 -
22b
Bhaumik K.Mali UW.Akamanchi KG. Synth. Commun. 2003, 33: 1603 - 23
Yadav JS.Reddy BVS.Jyothirmai B.Murty MSR. Tetrahedron Lett. 2005, 46: 6559 - 24
Eshghi H.Hassankhani A. Synth. Commun. 2006, 36: 2211 - 25
Xu L.-W.Xia C.-G.Li J.-W.Zhou S.-L. Synlett 2003, 2246 - 26
Loren JC.Sharpless KB. Synthesis 2005, 1514 - 27
Algi F.Balci M. Synth. Commun. 2006, 36: 2293