A Facile and Stereoselective Synthesis of Arylethers of Vicinal Bromohydrins by Mitsunobu Reaction

References

• Ariamala , G. and Balasubramanian , K. K. 1988 . J. Chem. Soc. Chem. Commun. , : 28
   Google Scholar
• Majumdar , K. C. and Kundu , A. K. 1992 . Indian. J. Chem. , 32B : 605
   Google Scholar
• Hepworth , J. D. 1984 . “ Comprehensive Heterocyclic Chemistry ” . Edited by: Katritzky , A. R. , Rees , C. W. , Boulton , A. J. and McKillop , A. Vol. 3 , pp. 742 Oxford : Pergamon Press .
   Google Scholar
• Livingstone , R. 1981 . “ Chromans and Tocopherols ” . Edited by: Ellis , G. P. Vol. 36 , pp. 161 New York : John Wiley & Sons .
   Google Scholar
• Mitsunobu , O. 1981 . Synthesis. , : 1
   Web of Science ®Google Scholar
• Roush , W. R. and Xiao-Fa , Lin . 1991 . J. Org. Chem. , 56 : 5740
   Web of Science ®Google Scholar
• Camp , D. and Jenkins , I. D. 1992 . Aus. J. Chem. ( , 45 : 47
   Web of Science ®Google Scholar
• Loibner , H. and Zbiral , E. 1976 . Heiv. Chim. Acta; , 59 : 2100
   Web of Science ®Google Scholar
• Colonge , J. and Guyot , A. 1958 . Bull. Soc. Chim. France. , : 325
   Google Scholar
• Cotterill , W. D. , Cottam , J. and Livingstone , R. 1970 . J. Chem. Soc. (C) , : 1006
   PubMedGoogle Scholar
• The coupling constant between H3 and H4 in compound 6c is found to be 1.92 Hz from the high resolution 1H nmr which could be well accountable for a diequatorial coupling, whereas in compound 6g the benzylic proton resonated at δ 5.48 as a doublet with J = 4.88 Hz. This was assigned for a pseudo diaxial coupling
   Google Scholar