An enantioconvergent approach to prostanoids

Journal of the Chemical Society, Chemical Communications

Volumn , Issue 10, 1978, Pages 436-438

  Trost, Barry M ^a   Timko, Joseph M ^a   Stanton, James L ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 37049096109     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39780000436     Document Type: Article

References (23)

1. For leading references see J S. Bindra,R. Bindra Prostaglandin Synthesis Academic Press New York 1977
2. A similar route to this compound appeared after our work was completed: M. Kato, M. Kageyama, R. Tanaka, K. Kuwahara, A. Yoshikoshi: J. Org. Chem. 1975, 40, 1932
3. LE. Overman: J. Amer. Chem. Soc., 1976, 98, 2901
4. ES. Lewis, JT. Hill: ibid., 1969, 917:458
5. WH. Pirkle, MS. Hoekstra: J. Org. Chem., 1974, 39, 3904
6. WH. Pirkle, JR. Hauske: ibid., 1977, 42, 2781
7. O. Ceder, B. Hansson: Acta Chem. Scand., 1970, 24, 2693
8. P. De Clerc, D. Van Haver, D. Tavernier, M. Vanderwalle: Tetrahedron, 1974, 30, 55
9. JL. Stanton: Thesis, Univer sity of Wisconsin 1975
10. GL. Bundy: Tetrahedron Letters 1975, 157
11. K. Kojima, K. Sakai: ibid., 1976, 101
12. CJ. Sih, JB. Heather, R. Sood, P. Price, G. Peruzzotti, LFH. Lee, SS. Lee, J. Amer. Chem. Soc., 1975,97,865 for anexample of kinetic resolution in introduction of the side chain see AF. Kluge KG. Untch and JH Fried ibid., 1972, 94, 9256
13. GH. Posner: Org. Reactions, 1972, 19, 1
14. A. Hamon, B. Lacoume, A. Oliver, WR. Pilgrim: Tetrahedron Letters, 1975, 4481
15. RK. Boeckman, KJ. Bruza, JE. Baldwin, OW. Lever: J.C.S. Chem. Comm. 1975, 519
16. RA. Ruden, WE. Litterer: Tetrahedron Letters, 1975, 2043
17. K. Alder, G. Stein: Annalem, 1934, 514, 197
18. AF. Thomas, B. Willhalm: Helv. Chim. Acta, 1967,50, 826
19. EJ. Corey, K. Narasaka, M. Shibasaki: J. Amer. Chem. SOC., 1976, 98, 6417
20. EW. Yankee, U. Axen, GL. Bundy: J. Amer. Chem. SOC., 1974, 96, 5865
21. Kindly supplied by Dr GL. Bundy: The rotation for this compound was not reported previously The optical purity wasestablished from its mode of synthesis from optically pure prostanoids and from its biological activity
22. F. Kienzle, GW. Holland, JL. Jernow, S. Kwoh, P. Rosen: J. Org. Chem., 1973, 38, 3440
23. CH. Kuo, D. Tauband, NL. Wendler: Tetrahedron Letters, 1972, 5317