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Synthesis 2009(20): 3467-3471
DOI: 10.1055/s-0029-1216969
DOI: 10.1055/s-0029-1216969
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of α-Aminonitriles through Strecker Reaction of N-Tosylaldimines Using Molecular Iodine [¹]
Further Information
Received
6 May 2009
Publication Date:
21 August 2009 (online)
Publication History
Publication Date:
21 August 2009 (online)
Abstract
The Strecker reaction of N-tosylaldimines with trimethylsilyl cyanide in the presence of catalytic amount of iodine at room temperature produces the corresponding protected α-aminonitriles in high yields.
Key words
Strecker reaction - N-tosylaldimine - trimethylsilyl cyanide - protected α-aminonitrile - iodine
Part 187 in the series, Studies on Novel Synthetic Methodologies.
-
2a
Shafran YM.Bakulev VA.Mokrushin VS. Russ. Chem. Rev. 1989, 58: 148 -
2b
March J. Advanced Organic Chemistry 4th ed.: Wiley; New York: 1999. p.965 -
3a
Weinstock LM.Davis P.Handlesman B.Tull R. J. Org. Chem. 1967, 32: 2823 -
3b
Matier WL.Owens DA.Comer WT.Deitchman D.Ferguson HC.Seidehamel RJ.Young JR. J. Med. Chem. 1973, 16: 901 -
4a
Chemistry and Biochemistry of the Amino Acids
Barrett GC. Chapman & Hall; London: 1985. -
4b
Coppala GM.Schuster HF. Asymmetric Synthesis Construction of Chiral Molecules Using Amino Acids Wiley; New York: 1987. and references cited therein -
5a
Duthaler RO. Tetrahedron 1994, 50: 1539 -
5b
Enders D.Shilvock P. Chem. Soc. Rev. 2000, 29: 359 -
6a
Strecker A. Ann. Chem. Pharm. 1850, 75: 27 -
6b
Yet L. Angew. Chem. Int. Ed. 2001, 40: 875 -
6c
Groger H. Chem. Rev. 2003, 103: 2795 -
7a
Harusawa S.Hamada Y.Shioiri T. Tetrahedron Lett. 1979, 20: 4663 -
7b
Mai K.Patil G. Tetrahedron Lett. 1984, 25: 4583 -
7c
Kobayashi S.Ishitani H. Chem. Rev. 1999, 99: 1069 -
7d
Davis FA.Lee S.Zhang H.Fanelli DL. J. Org. Chem. 2000, 65: 8704 -
7e
Mori Y.Kimura M.Seki M. Synthesis 2003, 2311 -
7f
Nakamura S.Sato N.Sugimoto M.Toru T. Tetrahedron: Asymmetry 2004, 15: 1513 -
7g
Herrera RP.Sagarzani V.Bernardi L.Fini F.Pettersen D.Ricci A. J. Org. Chem. 2006, 71: 9869 -
8a
Kobayashi S.Busujima T.Nagayama S. Chem. Commun. 1998, 981 -
8b
Bhanu Prasad BA.Bisai A.Singh VK. Tetrahedron Lett. 2004, 45: 9565 -
8c
Royer L.De S K.Gibbs RA. Tetrahedron Lett. 2005, 46: 4595 -
8d
Surya Prakash GK.Mathew T.Panja C.Alconcel S.Vaghoo H.Do C.Olah GA. Proc. Natl. Acad. Sci. U.S.A. 2007, 104: 3703 -
9a
Li BF.Yuan K.Zhang MJ.Wu H.Dai LX.Wang QR.Hou XL. J. Org. Chem. 2003, 68: 6264 -
9b
Takahashi E.Fujisawa H.Yanai T.Mukaiyama T. Chem. Lett. 2005, 34: 318 -
9c
Fetterly BM.Jana NK.Verkade JG. Tetrahedron 2006, 62: 440 -
10a
Groger H. Chem. Eur. J. 2001, 7: 5247 -
10b
Shibasaki M.Yoshikawa N. Chem. Rev. 2002, 102: 2187 -
10c
Tsogoeva SB.Heteley MJ.Yalalov DA.Meindl K.Weckbecker C.Huthmacher K. Bioorg. Med. Chem. 2005, 13: 5680 -
11a
Krueger CA.Kuntz KW.Dzierba CD.Wirschun WG.Gleason JD.Snapper ML.Hoveyda AH. J. Am. Chem. Soc. 1999, 121: 4284 -
11b
Banphavichit V.Mansawat W.Bhanthumnavin W.Vilaivan T. Tetrahedron 2004, 60: 10559 -
11c
Blacker J.Clutterbuck LA.Crampton MR.Grosjean C.North M. Tetrahedron: Asymmetry 2006, 17: 1449 -
12a
Iyer MS.Gigstad KM.Namdev ND.Lipton M. J. Am. Chem. Soc. 1996, 118: 4910 -
12b
Corey EJ.Grogan M. Org. Lett. 1999, 1: 157 -
12c
Sigman MS.Vachal P.Jacobsen EN. Angew. Chem. Int. Ed. 2000, 39: 1279 -
12d
Liu B.Feng X.Chen F.Zhang G.Cui X.Jiang Y. Synlett 2001, 1551 -
13a
Yadav JS.Reddy BVS.Eshwaraiah B.Srinivas M.Vishnumurthy P. New J. Chem. 2003, 27: 462 -
13b
Surendra K.Krishnaveni NS.Mahesh A.Rao KR. J. Org. Chem. 2006, 71: 2532 -
14a
Love BE.Raje SP.Williams TC. Synlett 1994, 493 -
14b
Liu G.Cogan DA.Owens TD.Tang TP.Ellman JA. J. Org. Chem. 1999, 64: 1278 -
14c
Chemla F.Hebbe V.Normant J. Synthesis 2000, 75 -
14d
Tang TP.Volkman SK.Ellman JA. J. Org. Chem. 2001, 66: 8772 -
14e
Ruano JG.Aleman J.Cid MB.Parra A. Org. Lett. 2005, 7: 179 -
15a
Fukuda Y.Maeda Y.Kondo K.Aoyama T. Synthesis 2006, 1937 -
15b
Fukuda Y.Kondo K.Aoyama T. Synthesis 2006, 2649 -
15c
Haung X.Haung J.Wen Y.Feng X. Adv. Synth. Catal. 2006, 348: 2579 -
15d
Kantam ML.Mahendar K.Sreedhar B.Choudary BM. Tetrahedron 2008, 64: 3351 - 16
Jennings WB.Lovely CJ. Tetrahedron 1991, 47: 5561 -
17a
Nandi P.Redko MY.Petersen K.Dye JL.Lefenfeld M.Vogt PF.Jackson JE. Org. Lett. 2008, 10: 5441 -
17b
Bajwa JS.Chen G.-P.Prasad K.Repic O.Blacklock TJ. Tetrahedron Lett. 2006, 47: 6425
References
Part 187 in the series, Studies on Novel Synthetic Methodologies.