A Logic-Based Program for Synthesis Design

Journal of the American Chemical Society

Volumn 107, Issue 18, 1985, Pages 5228-5238

  Hendrickson, James B ^a   Grier, David L ^a   Toczko, A Glenn ^a  

^a BRANDEIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001237629     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00304a033     Document Type: Article

References (17)

1. Hendrickson, J. B.; Braun-Keller, H.; Toczko, A. G. Tetrahedron, Suppl. 1981, 37, 359.
2. Hendrickson, J. B. J. Am. Chem. Soc. 1977, 99, 5439.
3. The procedure for canonical numbering of skeletons and their comparison for identity is detailed in: Hendrickson, J. B.; Toczko, A. G. J. Chem. Inf. Comput. Sci. 1983, 23, 171.
4. Spencer, T. A.; Newton, M. D.; Baldwin, S. W. J. Org. Chem. 1964, 29, 787; improved by Mr. Ing-Lung Shih in our laboratory.
5. Weiss, U.; Edwards, J. M. Tetrahedron Lett. 1968, 4885.
6. Hendrickson, J. B. J. Am. Chem. Soc. 1971, 93, 6847.
7. Hendrickson, J. B. J. Chem. Inf. Comput. Sci. 1979, 3, 129.
8. Hendrickson, J. B.; Braun-Keller, E. J. Comput. Chem. 1980, 1, 323.
9. Syntheses of estrone (and homoestrone) are reviewed: ApSimon, J. In “The Total Synthesis of Natural Products”; Wiley: New York, 1973; Vol. 2. Later syntheses: (a) Danishefsky, S.; Nagel, A. Chem. Commun. 1972, 373. (b) Cohen, N.; Banner, B. L.; Blount, J. F.; Tsai, M.; Saucy, G. J. Org. Chem. 1973, 38, 3229. (c) Bartlett, P. A.; Johnson, W. S. J. Am. Chem. Soc. 1973, 95, 7501. (d) Danishefsky, S.; Cain, P. Pure Appl. Chem 1975, 97, 5282; 1976, 98, 4975. (e) Kametani, T.; Nemoto, H.; Ishikawa, H.; Shiroyama, K.; Fukumoto, K. Pure Appl. Chem 1976, 98, 3378. (f) Oppolzer, W.; Battig, K.; Petrzilka, M. Helv. Chim. Acta 1978, 61, 1945. (g) Byron, T. A.; Reichel, C. J. Tetrahedron Lett. 1980, 2381. (h) Grieco, P. A.; Takigawa, T.; Schillinger, W. J. J. Org. Chem. 1980, 5, 2247. (i) Quinkert, G.; Weber, W.-D.; Schwartz, U.; Durner, G. Angew. Chem., Int. Ed. Engl. 1980, 19, 1027. (j) Stork, G.; Sherman, D. H. J. Am. Chem. Soc. 1982, 104, 3758.
10. Ananchenko, S. N.; Torgov, I. V. Tetrahedron Lett. 1963, 1553. Smith, H. et al. Experientia 1963, 19, 394; J. Chem. Soc. 1963, 5072.
11. Most of the jasmone syntheses are reviewed by Ho: Ho, T.-L. Synth. Commun. 1974, 4, 265. Subsequent syntheses: (a) Torii, S.; Tanaka, H.; Tomotaki, Y. Bull. Chem. Soc. Jpn. 1977, 50, 537. (b) Stetter, H.; Kuhlmann, H. Synthesis 1975, 379. (c) Pattenden, G.; Storer, R. J. Chem. Soc., Perkin Trans. 1 1974, 1603. (d) Murata, S.; Matsuda, I. Synthesis 1978, 221. (e) Wakamatsu, T.; Akasaka, K.; Ban, Y. Tetrahedron Lett. 1974, 3883. (f) Smith, A. B., III; Branca, S. J.; Toder, B. T. Pure Appl. Chem 1975, 4225. (g) Clark, R. D.; Kozar, L. G.; Heathcock, C. Synth. Commun. 1975, 5, 1.
12. Yoshida, T.; Yamaguchi, A.; Komatsu, A. Agri. Biol. Chem. 1966, 30, 370.
13. Frank, R. L.; Arvan, P. G.; Richter, J. W.; Vanneman, C. R. J. J. Am. Chem. Soc. 1944, 66, 4.
14. Elliott, J. J. Chem. Soc. 1956, 2231.
15. Wenkert, E.; Mueller, A.; Reardon, E. J.; Sathe, S. S.; Scharf, D. J.; Tosi, G. J. Am. Chem. Soc. 1970, 92, 7428.
16. Weinreb, S. M.; Cvetovich, R. J. Tetrahedron Lett. 1983, 861; J. Am. Chem. Soc. 1984, 106, 1443.
17. Snider, B. B.; Faith, W. C. Tetrahedron Lett. 1983, 861; J. Am. Chem. Soc. 1984, 106, 1443.