Advances in the chemistry of tetrahydroquinolines
V Sridharan, PA Suryavanshi, JC Menendez - Chemical reviews, 2011 - ACS Publications
1.1. General Heterocyclic compounds, especially nitrogen heterocycles, are the most
important class of compounds in the pharmaceutical and agrochemical industries, with …
important class of compounds in the pharmaceutical and agrochemical industries, with …
Advances in the reduction of quinolines to 1, 2, 3, 4‐tetrahydroquinolines
M El‐Shahat - Journal of Heterocyclic Chemistry, 2022 - Wiley Online Library
The pursuit of modern sustainable chemistry has stimulated the development of innovative
catalytic processes that enable chemical transformations to be performed under mild and …
catalytic processes that enable chemical transformations to be performed under mild and …
Chiral Phosphoric Acid-Catalyzed Synthesis of Fluorinated 5,6-Dihydroindolo[1,2-c]quinazolines with Quaternary Stereocenters
XW Wang, MW Chen, B Wu, B Wang… - The Journal of Organic …, 2019 - ACS Publications
A chiral phosphoric acid-catalyzed enantioselective synthesis of fluorinated 5, 6-
dihydroindolo [1, 2-c] quinazolines has been developed by a condensation/amine addition …
dihydroindolo [1, 2-c] quinazolines has been developed by a condensation/amine addition …
Asymmetric CH and NH Functionalization of Indoles Involving Central Chirality via Chiral Phosphoric Acid Catalysis
The CH and NH functionalization of indoles is an interesting area of research that has a
useful impact on organic synthesis due to the availability of chiral indole scaffolds in the …
useful impact on organic synthesis due to the availability of chiral indole scaffolds in the …
Chiral phosphoric acid-catalyzed regioselective synthesis of spiro aminals with quaternary stereocenters
XW Wang, MW Chen, B Wu, B Wang, B Wan, YG Zhou - Tetrahedron letters, 2021 - Elsevier
A chiral phosphoric acid-catalyzed enantioselective synthesis of spiro [indoline-3, 6′-indolo
[1, 2-c] quinazolin]-2-ones has been developed by condensation/N-alkylation cascade from …
[1, 2-c] quinazolin]-2-ones has been developed by condensation/N-alkylation cascade from …
Benzocaine as a precursor of promising derivatives: synthesis, reactions, and biological activity
Electrophilic and nucleophilic reactions of benzocaine are the most common procedures to
construct a library of benzocaine derivatives, which have promising features that could be …
construct a library of benzocaine derivatives, which have promising features that could be …
Catalyst-Free Synthesis of Aminals from Indole-Derived α, α-Dicyanoolefins
HL Cui, Y Shi, HQ Deng, JJ Lei, XJ Xu, X Tian, J Qiao… - Synlett, 2019 - thieme-connect.com
We have developed an efficient synthesis of indole fused aminals with nucleophilic imines
and indole-derived α, α-dicyanoolefins via N-sulfonyl group transfer. The combination of two …
and indole-derived α, α-dicyanoolefins via N-sulfonyl group transfer. The combination of two …
[HTML][HTML] Goniomitine: An Overview on the Chemistry of This Indole Alkaloid
JCF Alves - ISRN Organic Chemistry, 2013 - ncbi.nlm.nih.gov
Goniomitine: An Overview on the Chemistry of This Indole Alkaloid - PMC Back to Top Skip
to main content NIH NLM Logo Access keys NCBI Homepage MyNCBI Homepage Main …
to main content NIH NLM Logo Access keys NCBI Homepage MyNCBI Homepage Main …
[PDF][PDF] НОВЫЕ КОМБИНИРОВАННЫЕ ПРОИЗВОДНЫЕ НА ОСНОВЕ ПРИРОДНЫХ СОЕДИНЕНИЙ
ГК Мукушева - НАУЧНО-ПРАКТИЧЕСКИЙ ЖУРНАЛ, 2014 - phyto.kz
В представленном обзоре обобщены данные синтеза новых комбинированных
производных на основе молекул терпеноидов, алкалоидов, флавоноидов. Сочетание в …
производных на основе молекул терпеноидов, алкалоидов, флавоноидов. Сочетание в …