A Facile Microwave Assisted Synthesis and Antimicrobial Activities of Naturally Occurring (E)-Cinnamyl (E)-Cinnamates and (E)-Aryl Cinnamates. -A stereoselective method for the synthesis of (E)-cinnamyl (E)-cinnamate (III) and (E)-aryl cinnamate (V) usesWittig reaction under microwave irradiation. The products show antibacterial and antifungal activity. -(MAHAJAN, R. P.; PATIL, U. K.; PATIL*, S. L.; Indian J.
Carboxylic acid esters Q 0530 Convenient Microwave Assisted Synthesis of Naturally Occurring Methyl (E)-Cinnamates. -A stereoselective method is presented for the synthesis of methyl (E)-cinnamates (III) by the Wittig reaction under microwave irradiation. The method is efficient and affords the products in high yields. -(MAHAJAN, R. P.; PATIL*, S. L.; MALI, R. S.; Org. Prep. Proced. Int. 37 (2005) 3, 287-290; Sch. Chem. Sci., North Maharashtra Univ., Jalgaon 425 001, India; Eng.) -M. Bohle 42-098
Other natural products U 0800 Convenient Synthesis of (E)-Methyl O-Alkylferulates: Formal Synthesis of O-Geranylconiferyl Alcohol, a Metabolite of Fagara rhetza. -Two alternative routes for the stereoselective synthesis of (E)-methyl O-alkylferulates (V) from vanillin (I) are developed. Reduction of geranyl ether (Vc) provides the naturally occurring O-geranylconiferyl alcohol (VII). -(MAHAJAN, R. P.; PATIL*, S. L.; MALI, R. S.; Indian J.
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