References
- Lewln , A. and Goldberg , N. 1972 . Tet. Let. , 6 : 491
- Saegusa , T. and Murase , I. 1972 . Synthetic Communication Vol. 2 , 1 (#1)
- UUch , L. and Adams , R. 1921 . J. Amer. Chem. Soc. , 43 : 660 P ZnCk 9
- Pishnamazzade , B. and Gulieva , S. 1959 . C. A. , S3 : 4119f
- The above reaction condttions (ZnCl2) were unusuable for formation of functionalized (-OCH-Cl) aromatic esters due to non-selective reactions with the aromatic ring as well as the carboxylic acid group
- Taylor , E. , McLay , G. and McKillop , A. 1968 . J. Amer. Chem. Soc. , 90 : 2422
- Purdle , T. and Neave , G. 1910 . J. Chem. Soc. , 97 : 1517
- Satisfactory elemental analysis or mass spectral data were obtained for all compounds listed
- All boiling points listed are the oven temperatures reauired for bulb to bulb distillation at the pressure listed
- The halomethylene compound used in this preparation was CH2ClBr or better CH2Br2 (no halomethylene esters were isolated from this reaction)
- Not yet attempted
- The halomethylene compound was chloromethyl methyl ether
- The halomethylene compound was chloromethyl acetate