Facile oxidative cyclization and carbonylation of allylicalcohols
H Alper, D Leonard
Index: Alper, Howard; Leonard, Daniele Tetrahedron Letters, 1985 , vol. 26, # 46 p. 5639 - 5642
Full Text: HTML
Citation Number: 40
Abstract
Abstract Palladium chloride catalyzed reaction [room temperature, one atmosphere] of primary, secondary, and tertiary allylic alcohols with carbon monoxide and oxygen, hydrochloric acid, and cupric chloride in tetrahydrofuran affords five-membered ring lactones.
Related Articles:
Gefitinib or carboplatin–paclitaxel in pulmonary adenocarcinoma
[Bachi, Mario D.; Bosch, Eric Heterocycles, 1989 , vol. 28, # 2 p. 579 - 582]
[Stille, John R.; Grubbs, Robert H. Journal of Organic Chemistry, 1989 , vol. 54, # 2 p. 434 - 444]
Reaction of silyl ketene acetals with epoxides: a new method for the synthesis of γ-butanolides
[Maslak, Veselin; Matovic, Radomir; Saicic, Radomir N. Tetrahedron, 2004 , vol. 60, # 40 p. 8957 - 8966]
Highly regioselective ring-opening of α-substituted cyclic acid anhydrides catalyzed by lipase
[Tetrahedron Letters, , vol. 30, # 12 p. 1555 - 1556]
Synthesis of. gamma.-and. delta.-lactones by free-radical annelation of Se-phenyl selenocarbonates
[Bachi, Mario D.; Bosch, Eric Journal of Organic Chemistry, 1992 , vol. 57, # 17 p. 4696 - 4705]