Organic letters

Synthesis of substituted 3-hydroxy-2-furanone derivatives via an unusual enolate Wittig rearrangement/alkylative cyclization sequence

RK Everett, JP Wolfe

Index: Organic Letters, , vol. 15, # 12 p. 2926 - 2929

Full Text: HTML

Citation Number: 7

Abstract

... Volume: Page: ... Organic Letters. ... Upon workup, protonation of the enolate would generate 14, which can then undergo conjugate addition of water or hydroxide to provide alcohol 15.(13) Intramolecular acylation of the alcohol then yields the product 4.(14). ...

Related Articles:

Synthesis of Benzo [g] isochromenes through Photo??Dehydro??Diels–Alder Reaction

[Wessig, Pablo; Mueller, Gunnar; Herre, Robert; Kuehn, Andreas Helvetica Chimica Acta, 2006 , vol. 89, # 11 p. 2694 - 2719]

Asymmetric Organocatalytic Wittig [2, 3]-Rearrangement of Oxindoles

[Everett, Renata K.; Wolfe, John P. Organic Letters, 2013 , vol. 15, # 12 p. 2926 - 2929]

Preparation of arylpropiolate esters from trichlorocyclopropenium cation and elaboration of the esters to unsymmetrical 1, 4-pentadiyn-3-ones and unsymmetrical …

[Wadsworth, Donald H.; Geer, Susan M.; Detty, Michael R. Journal of Organic Chemistry, 1987 , vol. 52, # 16 p. 3662 - 3668]

Preparation of arylpropiolate esters from trichlorocyclopropenium cation and elaboration of the esters to unsymmetrical 1, 4-pentadiyn-3-ones and unsymmetrical …

[Journal of Organic Chemistry, , vol. 52, # 16 p. 3662 - 3668]

1-(1, 2, 5-Thiadiazol-4-yl)-4-azatricyclo [2.2. 1.02, 6] heptanes as New Potent Muscarinic M1 Agonists: Structure-Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3 …

[Journal of Medicinal Chemistry, , vol. 42, # 11 p. 1999 - 2006]

More Articles...