Synthesis, Table of Contents PAPER © Georg Thieme Verlag Stuttgart · New York Synthesis of l-ido-Configured Six- and Seven-Membered Carba-Sugars C. V. Ramana*, Siddhartha R. Chaudhuri, Mukund K. GurjarNational Chemical Laboratory, Pune-411 008, IndiaFax: +91(20)25902629; e-Mail: vr.chepuri@ncl.res.in; Recommend Article Abstract Buy Article All articles of this category Abstract Ring-closing olefin metathesis has been successfully applied to the modular construction of l-ido-configured six- and seven-membered carba-sugars. Key words allylations - carbocycles - carbohydrates - metathesis - radical reactions Full Text References References 1a Capila I. Linhardt RJ. Angew. Chem. Int. Ed. 2002, 41: 390 1b Fareed J. Hoppensteadt DA. Bick RL. Semin. Thromb. Hemost. 2000, 26: 5 1c Linhardt RJ. Gunay NS. Semin. Thromb. Hemost. 1999, 25: 5 2 Witczak ZJ. Nieforth KA. Carbohydrates in Drug Design Marcel Dekker; New York: 1997. 3a Mallet J.-M. Esnault J. Driguez P.-A. Duchaussoy P. Sizun P. Hérault J.-P. Herbert J.-M. Petitou M. Sinaӱ P. Angew. Chem. Int. Ed. 2001, 40: 1670 3b Das SK. Mallet J.-M. Esnault J. Driguez P.-A. Duchaussoy P. Herault J.-P. Herbert J.-M. Petitou M. Sinaӱ P. Chem. Eur. J. 2001, 7: 4821 4a Ferrier RJ. J. Chem. Soc., Perkin Trans. 1 1979, 1455 4b Ogawa S. Ara M. Kondoh T. Saitoh M. Masuda R. Toyokuni T. Suami T. Bull. Chem. Soc. Jpn. 1980, 53: 1121 4c Ogawa S. Tsukiboshi Y. Iwasawa Y. Suami T. Carbohydr. Res. 1985, 136: 77 4d Blattner R. Ferrier RJ. J. Chem. Soc., Chem. Commun. 1987, 1008 4e Paulsen H. von Deyn W. Liebigs Ann. Chem. 1987, 125 4f Barton DHR. Géro SD. Cléophax J. Machado AS. Quiclet-Sire B. J. Chem. Soc., Chem. Commun. 1988, 1184 4g Marco-Contelles J. Pozuelo C. Jimeno ML. Martinez L. Martinez-Grau A. J. Org. Chem. 1992, 57: 2625 4h Dalko PI. Sinaӱ P. Angew. Chem. Int. Ed. 1999, 38: 773 4i Sollogoub M. Pearce AJ. Hérault A. Sinaӱ P. Tetrahedron: Asymmetry 2000, 11: 283 4j Trotter NS. Larsen DS. Stoodley RJ. Brooker S. Tetrahedron Lett. 2000, 41: 8957 5 Gurjar MK. Chaudhuri SR. Tetrahedron Lett. 2002, 43: 2435 6 Parolis H. Carbohydr. Res. 1983, 114: 21 7a Fürstner A. Angew. Chem. Int. Ed. 2000, 39: 3013 7b Yet L. Chem. Rev. 2000, 100: 2963 For a latest comprehensive review on the utilization of RCM in carbohydrate chemistry, see: 7c Roy R. Das SK. Chem. Commun. 2000, 519 8a Manna S. Jacques YP. Falck JR. Tetrahedron Lett. 1986, 27: 2679 8b Gurjar MK. Patil VJ. Pawar SM. Carbohydr. Res. 1987, 165: 313 9 Sudha AVRL. Nagarajan M. Chem. Commun. 1998, 925 10 Barton DHR. Géro SD. Cléophax J. Machado AS. Quiclet-Sire B. J. Chem. Soc., Chem. Commun. 1988, 1184