An article Diastereoselective synthesis of highly substituted tetrahydroquinolines using benzoylacetonitrile via aza Diels-Alder reaction WOS:000650994000012 published article about STEREOSELECTIVE-SYNTHESIS; QUINOLINE DERIVATIVES; ASYMMETRIC-SYNTHESIS; CASCADE REACTIONS; POVAROV REACTION; CYCLIZATION; CHEMISTRY; FURANS; ACID in [Chen, Chinpiao] Tzu Chi Univ Sci & Technol, Dept Nursing, Hualien 970302, Taiwan; [Palanimuthu, Arunan; Chen, Chinpiao] Natl Dong Hwa Univ, Dept Chem, Hualien 974301, Taiwan; [Lee, Gene-Hsian] Natl Taiwan Univ, Coll Sci, Instrumentat Ctr, Taipei 10617, Taiwan in 2021.0, Cited 61.0. HPLC of Formula: C7H5NO3. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6
Diastereoselective aza-Diels-Alder reaction between in situ generated 2-aminophenyl-substituted enones and alpha-cyano-alpha,beta-unsaturated aromatic ketone has been developed. In the presence of TEA as a catalyst prepared highly substituted tetrahydroquinolines with an all-carbon quaternary center in an in situ fashion. Both tetrahydroquinoline isomers (exo and endo) with excellent diastereoselectivity and high yields were synthesized in very mild conditions. (C) 2021 Published by Elsevier Ltd.
HPLC of Formula: C7H5NO3. Welcome to talk about 99-61-6, If you have any questions, you can contact Palanimuthu, A; Chen, CP; Lee, GH or send Email.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem