REFERENCES
- He , Y. , Zhao , H. , Pan , X. and Wang , S. 1989 . Synth. Commun. , 19 : 3047
- Ayyanger , N. R. , Brahme , K. C. , Kalkote , U. R. and Srinivasan , K. V. 1984 . Synthesis , : 938
- Davies , R. R. and Hodgson , H. H. 1943 . J. Chem. Soc. , : 281
- Nishimura , S. 1961 . Bull. Chem. Soc. Jpn. , 34 : 32
- Corbett , J. F. 1968 . Chem. Commun. , : 1257
- Nystrom , R. F. and Brown , W. G. 1948 . J. Am. Chem. Soc. , 70 : 3739
- 1996 . “ Milos Hudlicky, ACS Monograph 188 ” . In Reductions in Organic Chemistry , 2nd ed. 91 – 101 . American Chemical Society .
- Bartoli , G. , Marcantoni , E. , Bosco , M. and Dalozzo , R. 1988 . Tetrahedron Letters , 29 : 2251
- Bartoli , G. , Marcantoni , E. and Petrini , M. 1990 . J. Org. Chem. , 55 : 4456
- Bartoli , G. , Marcantoni , E. and Petrini , M. 1991 . J. Chem. Soc. Chem. Commun. , 12 : 793
- Paul , A. Grieco , ed. 1998 . Organic Synthesis in Water UK : Blackie Academic & Professional .
- Li , C.-J. and Chan , T.-H. 1997 . Organic Reactions in Aqueous Media John Wiley & Sons, INC .
- Li , C.-J. and Chan , T.-H. 1999 . Tetrahedron , 55 : 11149
- Cintas , P. 1995 . Synlett , : 1087
- Several bases (e.g. diisoprophyl ethylamine, pyridine, DBU, K2CO3, CaCO3 etc) were tried
- When Entries 6 and 7 in Table 1 were reacted by Method B, N,N-diallylated products I and II were observed in 56% (I:II = 1.6:1) and 51% (I:II = 1.3:1) yield, respectively