Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
          
          https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
        Synthesis  2008(1): 122-126  
DOI: 10.1055/s-2007-1000828
   DOI: 10.1055/s-2007-1000828
PAPER
© Georg Thieme Verlag Stuttgart · New YorkHydroxylamine Derivatives as Nucleophiles in Ferrier Glycosylation: Synthesis of Aminoxy Pseudoglycals [1]
Further Information
            
               
                  
                        
                              Received
                              20 July 2007 
                      
Publication Date:
07 December 2007 (online)
            
         
      
   Publication History
Publication Date:
07 December 2007 (online)

Abstract
The use of hydroxylamine derivatives as the aminoxy equivalent nucleophiles in Ferrier glycosylation catalyzed by various acid catalysts is described. The reaction of tri-O-protected d-glucal with N-hydroxyphthalimide or N-hydroxysuccinimide was effectively promoted by a catalytic amount of zinc(II) chloride to produce the corresponding aminoxy pseudoglycal in good yields and preferential anomeric selectivity.
Key words
hydroxylamines - Ferrier glycosylation - pseudoglycals
IICT Communication No. 070126.
- 2a 
             
            Rodriguez EC.Marcaurelle LA.Bertozzi CR. J. Org. Chem. 1998, 63: 7134
- 2b 
             
            Marcaurelle LA.Rodriguez EC.Bertozzi CR. Tetrahedron Lett. 1998, 39: 8417
- 2c 
             
            Rodriguez EC.Winans KA.King DS.Bertozzi CR. J. Am. Chem. Soc. 1997, 119: 9905
- 2d 
             
            Cooper TS.Larigo AS.Laurent P.Moody CJ.Takle AK. Org. Biomol. Chem. 2005, 3: 1252
- 2e 
             
            Moody CJ. Chem. Commun. 2004, 1341
- 2f 
             
            Atobe M.Yamazaki N.Kibayashi C. J. Org. Chem. 2004, 69: 5595
- 2g 
             
            Hunt JCA.Laurent P.Moody CJ. J. Chem. Soc., Perkin Trans. 1 2002, 2378
- 3 
             
            Cervini SE.Dumy P.Mutter M. Angew. Chem., Int. Ed. Engl. 1996, 35: 1230
- 4 
             
            Li X.Yang D. Chem. Commun. 2006, 3367
- 5 
             
            Renaudet O.Dumy P. Tetrahedron Lett. 2001, 42: 7575
- 6a 
             
            Fraser-Reid B. Acc. Chem. Res. 1985, 18: 347
- 6b 
             
            Ferrier RJ. Adv. Carbohydr. Chem. Biochem. 1969, 24: 199
- 6c 
             
            Dorgan BJ.Jackson RFW. Synlett 1996, 859
- 6d 
             
            Schmidt RR.Angerbauer R. Angew. Chem., Int. Ed. Engl. 1977, 16: 783
- 6e 
             
            Schmidt RR.Angerbauer R. Carbohydr. Res. 1979, 72: 272
- 6f 
             
            Borrachero-Moya P.Cabrera-Escribano F.Gomez-Guillen M.Peredes-Leon MR. Carbohydr. Res. 1998, 308: 181
- 6g 
             
            Schmidt RR.Angerbauer R. Carbohydr. Res. 1981, 89: 159
- 6h 
             
            Danishefsky SJ.Bilodeau MT. Angew. Chem., Int. Ed. Engl. 1996, 30: 1357
- 6i 
             
            Bussolo VD.Kim Y.-J.Gin DY. J. Am. Chem. Soc. 1998, 120: 13515
- 6j 
             
            Tolstikov AG.Tolstikov GA. Russ. Chem. Rev. 1993, 62: 579
- 7a 
             
            Ferrier RJ.Prasad N. J. Chem. Soc. C 1969, 1: 570
- 7b For a review on the Ferrier rearrangement, see:  
            Ferrier RJ. Top. Curr. Chem. 2001, 215: 153
- 7c For a review on glycosidation, see:  
            Toshima K.Tatsuta K. Chem. Rev. 1993, 93: 1503
- 8a 
             
            Takhi M.Abdel-Rahman AA.-H.Schmidt RR. Tetrahedron Lett. 2001, 42: 4053
- 8b 
             
            Yadav JS.Reddy BVS.Chand PK. Tetrahedron Lett. 2001, 42: 4057
- 8c 
             
            Yadav JS.Reddy BVS.Raman JV.Niranjan N.Kumar SK.Kunwar AC. Tetrahedron Lett. 2002, 43: 2095
- 8d 
             
            Das KS.Reddy KA.Abbineni C.Roy J.Rao KVLN.Sachwani RH.Iqbal J. Tetrahedron Lett. 2003, 44: 4507 ; and references cited therein
- 9a 
             
            Chandrasekhar S.Reddy ChR.Chandrashekar G. Tetrahedron Lett. 2004, 45: 6481
- 9b 
             
            Yadav JS.Reddy BVS. Synthesis 2002, 511
- 9c 
             
            Houston TA.Chervin SM.Koreeda M. ITE Lett. Batter. New Technol. Med. 2002, 3: 23
- 9d 
             
            Kawabata H.Kubo S.Hayashi M. Carbohydr. Res. 2001, 333: 153 ; and references cited therein
- 10a 
             
            Smitha G.Reddy ChS. Synthesis 2004, 834
- 10b 
             
            Bettadaiah BK.Srinivas P. Tetrahedron. Lett. 2003, 44: 7257
- 10c 
             
            Shanmugasundaram B.Bose AK.Balasubramanian KK. Tetrahedron Lett. 2002, 43: 6795
- 10d 
             
            Swamy NR.Venkateshwarlu Y. Synthesis 2002, 598
- 10e 
             
            Takhi M.Abdel-Rahman AA.-H.Schmidt RR. Synlett 2001, 427
- 10f 
             
            Masson C.Soto J.Bessodes M. Synlett 2000, 1281
- 10g 
             
            Yadav JS.Reddy BVS.Murthy CVSR.Kumar GM. Synlett 2000, 1450
- 10h 
             
            Babu BS.Balasubramanian KK. Tetrahedron Lett. 1999, 40: 5777
- 11a 
             
            Yadav JS.Reddy BVS.Geetha V. Synth. Commun. 2003, 33: 717
- 11b 
             
            Babu BS.Balasubramanian KK. Tetrahedron Lett. 1999, 40: 5777 ; and references cited therein
- 12 
             
            Rajendra M.Srivastava RM.Oliveira FJS.da Silva LP.Filho JRF.Oliveira SP.Lima VLM. Carbohydr. Res. 2001, 332: 335 ; in this report the authors used BF3·OEt2 as a catalyst in benzene and observed the formation of only the α-anomer
- 13 
             
            Reddy ChR.Kiranmai N.Kiran Babu GS.Sarma DG.Jagadeesh B.Chandrasekhar S. Tetrahedron Lett. 2007, 48: 215
- 14a 
             
            Miyabe H.Yoshida K.Yamaguchi M.Takemoto Y. J. Org. Chem. 2005, 70: 2148
- 14b 
             
            Miyabe H.Matsumura A.Moriyama K.Takemoto Y. Org. Lett. 2004, 6: 4631
- 14c 
             
            Miyabe H.Yoshida K.Matsumura A.Yamaguchi M.Takemoto Y. Synlett 2003, 567
- 16 These types of compounds are useful advanced intermediates for making bio-active molecules,
            see:  
            Tejler J.Leffler H.Nilsson UJ. Bioorg. Med. Chem. Lett. 2005, 15: 2343
- 17 For bio-active molecules, see:  
            Thomas M.Rivault F.Tranoy-Opalinski I.Roche J.Gesson J.-P.Papot S. Bioorg. Med. Chem. Lett. 2007, 17: 983
References
IICT Communication No. 070126.
15This product showed hypolipidemic activity in mice, see ref. 12.
 
    