Enantioselective Reduction of Prochiral Ketones Using a Reagent Prepared from Lithium Aluminium Hydride, (+)Threo-1,16-Dibenzyloxy, 7(R),8(R)-Dihydroxy Hexadecane and Alcohol

References

• de Vries , F. J. , Brussee , J. , Kruse , C. G. and Vander Gen , A. 1994 . Tet. Asymmetry , 5 ( 3 ) : 377
   Web of Science ®Google Scholar
• Ivan Steels and De clercq , P. J. 1992 . Tet. Asymmetry , 3 ( 5 ) : 599
   Web of Science ®Google Scholar
• Trost , B. M. and Fleming , I. 1991 . Comphrehensive Organic Synthesis , Edited by: Nishizawa , M. and Noyori , R. Vol. 8 , 159 Pergamon Press .
   Google Scholar
• Bothner-By , A. A. 1951 . J. Am. Chem. Soc. , 73 : 846
   Google Scholar
• Cervika , O. 1965 . Collect. Czech. Chem. Commun. , 30 : 1684
   Google Scholar
• Cervika , O. and Belovsky , O. 1967 . Collect. Czech. Chem. Commun. , 32 : 3897
   Google Scholar
• Landor , S. R. , Miller , B. J. and Tatchell , A. R. 1966 . J. Chem. Soc. (C) , : 1822
   Web of Science ®Google Scholar
• 1967 . : 197
   Google Scholar
• Yamaguchi , S. , Mosher , H. S. and Pohland , A. 1972 . J. Am. Chem. Soc. , 94 : 9254
   Google Scholar
• Meyers , A. I. and Kendall , P. M. 1974 . Tetrahedron Lett. , : 1337
   Google Scholar
• Noyori , R. , Tomino , I. and Tanimoto , Y. 1979 . J. Am. Chem. Soc. , 101 : 3129
   Web of Science ®Google Scholar
• Noyori , R. , Tomino , I. , Tanimoto , Y. and Nishizawa , M. 1984 . J. Am. Chem. Soc. , 106 : 6709
   Web of Science ®Google Scholar
• McGhie , J. F. , Ames , D. E. , Goodburn , T. G. and Jevans , A. W. 1968 . J. Chem. Soc. (C) , : 268
   Web of Science ®Google Scholar
• Mukhopadhyay , B. and Muthana , M. S. , eds. 1962 . A monograph on lac , Ranchi : Indian LacResearch Institute .
   Google Scholar
• “J. Am. Oils Chemist's Soc.” , Accepted topublish in
   Google Scholar
• Landor , S. R. , Miller , B. J. and Tatchell , A. R. 1967 . J. Chem. Soc. (C) , : 197
   Google Scholar
• Procedure for the preparation of (R)-hydnocarpic alcohol: Chaulmoogra oil was transesterified to give methyl esters of chaulmoogra fatty acids. These methyl esters were then fractionated using 1ft. column packed with Dixon rings and fitted with perkin triangle on an oil bath under vacuum. Hydnocarpic methyl ester fraction collected (oil bath temp. 230°C, Drop temp. 144—146°C, under 1mm vacuum). This was then reduced with LAH to give an alcohol. Supported by 1HNMR, IR, GC-MS data
   Google Scholar
• Zang , Ya-Wen. , Shen , Zong-Xuan. , Liu , Cui-Ling. and Chen , Wei-Yi. 1995 . Synthetic communication , : 3407
   Google Scholar
• Forenasier , R. , Reniero , F. , Scrimin , P. and Tonellato , U. 1985 . J. Org. Chem. , 50 : 3209
   Google Scholar
• Ashby , E. C. and Boone , J. R. 1976 . J. Org. Chem. , 41 : 2890 5524
   Web of Science ®Google Scholar
• Felkin , H. 1951 . Bull. Soc. Chim. Fr. , 18 : 347
   Google Scholar
• Sweeting , Linda , Crans , D. C. and Whitesides , G. M. 1987 . J. Org. Chem. , 52 : 2273
   Web of Science ®Google Scholar