Facile synthesis of enantiopure tricyclic furanyl derivatives via tungsten-mediated cycloalkenation reactions and Diels–Alder reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
2. Synthetic studies on terpenoids. Part 24. Stereocontrolled synthesis of 3αβ-H,3bα-H,5aα-H,9aα-H,11aβ-H-9bβ-Methylperhydrophenanthro-[2,1-b]furan-7-one, an intermediate to epoxynorcafestanone
3. Aromatic NN exchange reactions of N,N-dimethylamino gem-difluorinated heterocycles. A convenient synthesis of new 5-imidazol-1-yl α,α-difluoroketones
4. Intramolecular palladium-catalyzed 1,4-addition to conjugated dienes. Stereoselective synthesis of fused tetrahydrofurans and tetrahydropyrans
5. Catalytic Iron-Mediated Enediene Carbocyclizations: Investigations into the Stereoselective Formation of Bicyclic Ring Systems
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