Substituent Effect on the Formation of Arylindanes by Dimerization of Ferulic Acid and its Related Compounds
Author:
Affiliation:
1. Department of Applied Chemistry and Biochemistry, National Institute of Technology, Wakayama College, 77 Noshima, Nada, Gobo̅, Wakayama 644-0023, Japan
2. Industrial Technology Center of Wakayama Prefecture, 60 Ogura, Wakayama 649-6261, Japan
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.8b01953
Reference24 articles.
1. AlCl3-Promoted Formal [2 + 3]-Cycloaddition of 1,1-Cyclopropane Diesters with N-Benzylic Sulfonamides To Construct Highly Stereoselective Indane Derivatives
2. Asymmetric synthesis of 1,2,3-trisubstituted indanes via an enantioselective copper(II)-catalyzed asymmetric nitroaldol reaction followed by an intramolecular Michael cyclization
3. Scope of the formal [3+2] cycloaddition for the synthesis of five-membered ring of functionalized indanes
4. Structural Revision and Total Synthesis of Caraphenol B and C
5. Enantioselective Copper-Catalyzed Reductive Michael Cyclizations
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3. Gold-Catalyzed Formal (3+2) Cycloaddition in an Ionic Liquid: Environmentally Friendly and Stereoselective Synthesis of Polysubstituted Indanes from Benzylic Alcohols and 1-Phenylpropenes;Synlett;2022-12-21
4. In search of new cinnamic acid derived flavours and fragrances;Results in Chemistry;2019-01
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