A Facile Synthesis of an (E)-4-Methyl-4-Hexenoic Acid Substituted Pyridine Analogue of Mycophenolic Acid

References

• Carter , S. B. , Franklin , T. J. , Jones , D. F. , Leonard , B. J. , Mills , S. D. and Turner , W. B. 1969 . Nature , 223 : 848
   PubMed Web of Science ®Google Scholar
• Nelson , P. H. , Eugui , E. , Wang , C. C. and Allison , A. C. 1990 . J. Med. Chem. , 33 : 833 and references cited therein
   PubMed Web of Science ®Google Scholar
• Hedstrom , L. and Wang , C. C. 1990 . Biochemistry , 29 : 849 and references cited therein
   PubMed Web of Science ®Google Scholar
• Lintrup , J. , Hyltoft-Petersen , P. , Knudtzon , S. and Nissen , N. I. 1971 . Cancer Chemother. Rep. Part I , 56 : 229
   Google Scholar
• Jones , D. F. and Mills , S. D. 1971 . J. Med. Chem. , 14 : 305
   PubMed Web of Science ®Google Scholar
• Canonica , L. , Rindone , B. , Santaniello , E. and Scolastico , C. 1972 . Tetrahedron , 28 : 4395 and references cited therein
   Web of Science ®Google Scholar
• Danheiser , R. L. , Gee , S. K. and Perez , J. J. 1986 . J. Am. Chem. Soc. , 108 : 806
   Web of Science ®Google Scholar
• Birch , A. J. and Wright , J. 1969 . J. Aust. J. Chem. , 22 : 2635
   Web of Science ®Google Scholar
• Reactions of 2-lithiopyridine and 2-bromo-6-lithiopyridine (which were prepared from 2-bromopyridine and 2,6-dibromopyridine using n-butyllithium in ether at −78 °C, respectively) with (E)-1-bromo-6-(tert-butyldimethylsiloxy)-3-methyl-2-hexene led only to recovered starting materials
   Google Scholar
• Boekelheide , V. , Fritz , H. , Ross , J. M. and Kaempfen , H. X. 1964 . Tetrahedron , 20 : 33
   Web of Science ®Google Scholar
• Guthrie , A. E. , Semple , J. E. and Joulie , M. M. 1982 . J. Org. Chem. , 47 : 2369 and references cited therein
   Web of Science ®Google Scholar
• Greene , T. W. 1981 . “Protective Groups in Organic Synthesis” , 122 – 128 . New York : John Wiley & Sons, Inc. .
   Google Scholar
• Gilman , N. W. 1971 . Chem. Comm. , : 733
   Web of Science ®Google Scholar