Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Patent
1989-12-13
1992-05-12
Gerstl, Robert
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
560121, C07C17700
Patent
active
051130149
ABSTRACT:
A process for the preparation of a prostaglandin of the formula ##STR1## wherein n is 1, 2, 3 or 4, R.sub.1 and R.sub.2, independently of each other, are alkyl, OH, alkoxy, ketone, halogen, hydrogen, nitro, amino or ether,
REFERENCES:
Journal of the American Chemical Society Nov. 29, 1972; Efficient Generation of the 15S Configuration in Prostaglandin Synthesis. Attractive Interactions in Stereochemical Control of Carbonyl Reduction. pp. 8616-8618.
Journal of the American Chemical Society 1988; pp. 4718-4726; The Three-Component Coupling Synthesis of Prostaglandins. M. Suzuki, et al vol. 110.
Journal of the American Chemical Society, 1988, vol. 110; pp. 4726-4735 Triply Convergent Synthesis of (-)-Prostaglandin E.sub.2 Methyl Ester; Carl R. Johnson et al.
Communications to the Editor; pp. 4745-4746; A General Approach to Prostaglandins via Methylenecyclopentanones. Total Synthesis of (.+-.)-Prostaglandin F.sub.2.alpha. (1975).
Communications to the Editor pp. 5843-5844; (1979).
Tetrahedron Letters, vol. 23, No. 39 pp. 4057-4060, 1982; A Facile Synthesis of (-)-Prostaglandin E.sub.1 Via a Three-Component Coupling Process M. Suzuki et al.
Tetrahedron Letters, vol. 27, No. 20, pp. 2199-2202, 1986; A New Synthetic Route to Prostaglandins; E. J. Corey et al.
Tetrahedron Letters, vol. 28, No. 46, pp. 5655-5658, 1987; Synthesis of Novel Prostaglandin F.sub.2 Isomers and structure of an enzymatically formed 13-Hydroxyprostaglandin Endoperoxide; Ute Hofmann et al.
Angew. Chemical Int. Ed. Engl. 22 1983; pp. 803-815; From Studies of Biochemical Mechanism to Novel Biological Mediators: Prostaglandin Endoperoxides Thromboxanes, and Leukotrienes (Nobel Lecture).
Danishefsky et al., I JACS 111, 3456 (1989).
Danishefsky et al., II JOC 54 6016 (1989).
Danishefsky et al. JACS 111 2599 (1989).
Chow Ken H.
Danishefsky Samuel J.
Naves Carmen M. P. C.
Gerstl Robert
Yale University
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