69258-09-9Relevant articles and documents
Dinuclear zinc catalyzed asymmetric spirannulation reaction: An umpolung strategy for formation of α-alkylated-α-hydroxyoxindoles
Trost, Barry M.,Hirano, Keiichi
supporting information; experimental part, p. 2446 - 2449 (2012/07/27)
A highly diastereo- and enantioselective formal [3 + 2] cycloaddition of α,β-unsaturated esters and 3-hydroxyoxindoles catalyzed by a dinuclear zinc-ProPhenol complex is reported. The stereoselective Michael additions of 3-hydroxyoxindoles and the subsequent transesterifications afford spirocyclic δ-lactones.
Syntheses and QSAR studies of sorbic, cinnamic and ricinoleic acid derivatives as potential antibacterial agents
Narasimhan,Kothawade,Pharande,Mourya,Dhake
, p. 2828 - 2834 (2007/10/03)
Amides and esters of sorbic, cinnamic and ricinoleic acid have been synthesized and evaluated for their antibacterial activity against gram (+) ve S. aureus, B. subtilis and gram (-) ve E. coli. Most of the compounds have shown moderate to good activity against microorganisms under test. Linear regression analysis of descriptors related to lipophilicity, steric and electronic parameters against antibacterial activity have been performed. QSAR studies indicated the predominance of electronic and steric parameters over the lipophilicity parameters in contributing antibacterial activity.
3,5-HEXADIENOIC ESTERS: A CONVENIENT PREPARATION
Hoye, Thomas R.,Magee, Andrew S.,Trumper Wendy S.
, p. 183 - 188 (2007/10/02)
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