A Triflate Hydrodeoxygenation Route to Resveratrol from Syringaldehyde

MC Davis, DA Parrish, BG Harvey

Index: Davis, Matthew C.; Parrish, Damon A.; Harvey, Benjamin G. Organic Preparations and Procedures International, 2013 , vol. 45, # 4 p. 304 - 313

Full Text: HTML

Citation Number: 5

Abstract

When a starting material is being contemplated for the synthesis of an active pharmaceutical ingredient or a building block for polymers, natural products are the green alternatives to petroleum feedstocks. 1, 2 Plant metabolites are an excellent source for aromatic compounds but are invariably oxygenated. 3–5 In certain cases, the hydroxy groups of the natural products are ideally located and can be simply built upon or protected to allow for ...

Related Articles:

Clean and selective oxidation of aromatic alcohols using silica-supported Jones' reagent in a pressure-driven flow reactor

[Wiles, Charlotte; Watts, Paul; Haswell, Stephen J. Tetrahedron Letters, 2006 , vol. 47, # 30 p. 5261 - 5264]

Benzyltriphenylphosphonium dichromate as a mild reagent for the oxidation of organic compounds

[Hajipour, Abdol Reza; Mohammadpoor-Baltork, Iraj; Niknam, Kurosh Organic Preparations and Procedures International, 1999 , vol. 31, # 3 p. 335 - 341]

Straightforward synthesis of aromatic imines from alcohols and amines or nitroarenes using an impregnated copper catalyst

[Perez, Juana M.; Cano, Rafael; Yus, Miguel; Ramon, Diego J. European Journal of Organic Chemistry, 2012 , # 24 p. 4548 - 4554]

A simple and efficient synthesis of 5'-(2H3) olivetol

[Canadian Journal of Chemistry, , vol. 65, p. 189 - 190]

Chemical studies on the heartwood of Cassia garrettiana Craib. III. Structures of two new polyphenolic compounds.

[Chemical & Pharmaceutical Bulletin, , vol. 36, # 8 p. 2977 - 2983]

More Articles...