The Still-Wittig Rearrangement in the Preparation of a Synthetically Useful 4C-Hydroxymethyl-hex-2-eno-pyranoside

References

• Fraser-Reid , B. 1985 . Acc. Chem. Res. , 18 : 347
   Web of Science ®Google Scholar
• Holder , N. 1982 . Chem. Rev. , 82 : 287
   Web of Science ®Google Scholar
• Ferrier , R. J. 1969 . Adv. Carbohydr. Chem. Biochem. , 24 : 199
   PubMedGoogle Scholar
• See ref. 1
   Google Scholar
• Hanessian , S. 1983 . Total Synthesis of Natural Products. The Chiron Approach. , Oxford : Pergamon Press .
   Google Scholar
• Inch , T. D. 1984 . Tetrahedron , 40 : 3194
   Google Scholar
• Pelyvas , I. , Lindhorst , T. and Thiem , J. 1990 . Liebigs Ann. Chem. , : 761 and refs. cited. For leading references
   Google Scholar
• Tulshian , D. B. and Fraser-Reid , B. 1984 . J. Org. Chem. , 49 : 518 and refs. cited
   Google Scholar
• Marshall , J. A. 1991 . The Wittig Rearrangement , Edited by: Trost , B. M. and Fleming , I. vol. 3 , 975 Pergamon Press . Recent reviews:
   Google Scholar
• Bruckner , R. 1991 . [2,3]-Sigmatropic Rearrangement , Edited by: Trost , B. M. and Fleming , I. vol. 6 , 873 Pergamon Press .
   Google Scholar
• Nakai , T. and Mikami , T. 1986 . Chem. Rev. , 86 : 885
   Web of Science ®Google Scholar
• Udodong , U. K. and Fraser-Reid , B. 1989 . J. Org. Chem. , 54 : 2103 and refs. cited
   Google Scholar
• Hanessian , S. and Lavallee , P. 1975 . Can. J. Chem. , 53 : 2975
   Web of Science ®Google Scholar
• Munavu , R. M. and Szmant , H. H. 1976 . J. Org. Chem. , 41 : 1832
   Web of Science ®Google Scholar
• Bessodes , M. , Abushanab , E. and Panzica , R. P. 1981 . J. Chem. Soc., Chem. Commun. , : 26
   Google Scholar
• Cf. Thiem and coworkers3a have observed the lost of the 6-O-(t-butyldiphenylsily) protecting group in the Tipson-Cohen reductive-elimination of the corresponding 3,4-di-O-mesylate
   Google Scholar
• Still , W. C. 1978 . J. Am. Chem. Soc. , 100 : 1481
   Web of Science ®Google Scholar
• Jarosz , S. and Fraser-Reid , B. 1989 . Tetrahedron Lett. , 30 : 2359 would result in the decrease in the “effective” concentration of n-BuLi if 1.5 equivalent were used. The use of excess n-BuLi was based on the premise that coordination of the lithium cation to the oxygens of the sugar moiety (cf.
   Web of Science ®Google Scholar
• Wee , A. G. H. 1990 . Tetrahedron , 46 : 5065
   Google Scholar