1-4-dihydroquinoline and triethylamine

1-4-dihydroquinoline has been researched along with triethylamine* in 1 studies

Other Studies

1 other study(ies) available for 1-4-dihydroquinoline and triethylamine

Article	Year
An organocatalytic cascade approach toward polysubstituted quinolines and chiral 1,4-dihydroquinolines-unanticipated effect of N-protecting groups. Angewandte Chemie (International ed. in English), 2012, Jul-16, Volume: 51, Issue:29 A matter of protection: The outcome of a divergent organocatalytic aza-Michael/aldol cascade process toward quinolines and 1,4-dihydroquinolines depends on the choice of the N-protecting group (see scheme; TEA = triethylamine, TMS = trimethylsilyl). Use of an electron-donating sulfonyl group results in an unanticipated aza-Michael/aldol/aromatization cascade to give polysubstituted quinolines (right). In contrast, chiral 1,4-dihydroquinolines are obtained with an electron-withdrawing sulfonyl group (left). Topics: Aldehydes; Catalysis; Electrons; Ethylamines; Quinolines; Trimethylsilyl Compounds	2012

Article

Year

An organocatalytic cascade approach toward polysubstituted quinolines and chiral 1,4-dihydroquinolines-unanticipated effect of N-protecting groups.

Angewandte Chemie (International ed. in English), 2012, Jul-16, Volume: 51, Issue:29

A matter of protection: The outcome of a divergent organocatalytic aza-Michael/aldol cascade process toward quinolines and 1,4-dihydroquinolines depends on the choice of the N-protecting group (see scheme; TEA = triethylamine, TMS = trimethylsilyl). Use of an electron-donating sulfonyl group results in an unanticipated aza-Michael/aldol/aromatization cascade to give polysubstituted quinolines (right). In contrast, chiral 1,4-dihydroquinolines are obtained with an electron-withdrawing sulfonyl group (left).

Topics: Aldehydes; Catalysis; Electrons; Ethylamines; Quinolines; Trimethylsilyl Compounds

2012