References
- Polonsky , J. , Johnson , B. C. , Cohen , P. E and Lederer , E. 1963 . Bull. Soc. Chim. Fr. , : 1909
- Mengzheng , Y. and Xiaolan , W. 1992 . Huaxue Shiji , 14 : 367 (C.A. 118:191255z)
- Chaudhuri , M. K. , Chettri , S. K. , Lyndem , S. , Paul , P. C. and Srinivas , P. 1994 . Bull. Chem. Soc. Jap. , 67 : 1894
- Skarzewski , J. 1984 . Tetrahedron , 40 : 4997
- Tamarkin , D. and Benny Rabinovitz , D. M. 1984 . Angew. Chem. Int. Ed. Engl. , 23 ( 6 ) : 642
- Tarmarkin , D. and Rabinovitz , M. 1987 . J. Org. Chem. , 52 : 3472
- de Vriess , J. B. and Hubbard , S. A. 1988 . J. Chem. Soc., Chem. Connun. , : 1172
- Lantos , I. 1978 . Tetrahedron Lett. , 31 : 2761
- Mallory , F. B. and Mallory , C. W. 1984 . Photocyclization of Stilbenes and Related Molecules , 1 – 456 . NY : John Willey & Sons .
- Liu , L. , Yang , B. , Katz , T. J. and Poindexter , M. K. 1991 . J. Org. Chem. , 56 : 3769
- Ide , W. S. and Buck , J. S. 1948 . Synthesis of Benzoin , 269 – 308 . NY : John Willey & Sons .
- Rubin , M. B. and Neuwirth-Weiss , Z. 1972 . J. Am. Chem. Soc. , 94 : 6048
- Washburn , R. M. , Levens , E. , Albright , C. F. , Billig , F. A. and Cernak , E. S. 1959 . Advances in Chemistry Series , 23 : 102 – 128 .
- Letsinger , R. L. and Hamilton , S. B. 1960 . J. Org. Chem. , 25 : 592
- Summerbell , R. K. and Berger , D. R. 1959 . J. Am. Chem. Soc. , 81 : 633
- Inoue , Y. , Harino , H. , Nakazato , T. , Koseki , N. and Hakushi , T. 1985 . J. Org. Chem. , 50 : 5151
- Lopez , L. and Calò Fiorentino , M. 1985 . J. Chem. Soc. Perkin Trans. I , : 457
- Blossey , E. C. , Neckers , D. C. , Thayer , A. L. and Schaap , A. P. 1973 . J. Am. Chem. Soc. , 95 ( 17 ) : 5820
- The yield of benzoin was 83%, 4,4′-dimethoxibenzoin was 75%, 4,4′-dichlorobenzoin was 67%, 4,4′-dimethylbenzoin was 61%, and 4-methoxy benzoin was 25%.
- Weis , C. D. 1968 . Helv. Chim. Acta , 51 ( 7 ) : 1572
- This signal disappeared upon addition of D2O.
- No ketal was obtained.
- The same melting point and infrared spectra.