Elimination Reactions of N-Alkyl-N-chlorothenylamines Promoted by MeONa−MeOH and Et2NH−MeCN. Effect of the β-Aryl Group on the Imine-Forming Transition State
Author:
Affiliation:
1. Department of Chemistry, Pukyong National University, Pusan 608-737, Korea, and Department of Chemistry, Korea University, 1-Anamdong, Seoul 136-701, Korea chobr@korea.ac.kr; sypyun@pknu.ac.kr
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo050368k
Reference21 articles.
1. Base-promoted, imine-forming 1,2-elimination reactions
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3. Complexation of neutral molecules by preorganized macrocyclic hosts
4. Reactions of N-halo-N-methylbenzylamines with sodium methoxide-methanol and potassium tert-butoxide-tert-butyl alcohol. Effects of .beta.-carbon substituent and base-solvent system upon the imine-forming transition state
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