Direct one-pot synthesis of Luotonin F and analogues via rational logical design

Y Zhu, Z Fei, M Liu, F Jia, A Wu - Organic letters, 2013 - ACS Publications
An efficient one-pot synthetic protocol has been proposed for the synthesis of luntonin F from
easily available starting materials. Through a rational logical design, multifundamental …

Pyridones–powerful precursors for the synthesis of Alkaloids, their derivatives, and alkaloid-inspired compounds

JG Sośnicki, TJ Idzik - Synthesis, 2019 - thieme-connect.com
2-Pyridone is characterized by a very wide range of reactivity of a different nature, ranging
from electrophilic aromatic substitution, CH–metal-mediated reactions, and NH/OH …

Development of Diphenylamine‐Linked Bis (imidazoline) Ligands and Their Application in Asymmetric Friedel–Crafts Alkylation of Indole Derivatives with …

H Liu, DM Du - Advanced Synthesis & Catalysis, 2010 - Wiley Online Library
The new diphenylamine‐linked bis (imidazoline) ligands were prepared through Kelly‐You's
imidazoline formation procedure mediated by Hendrickson's reagent in good yields. The …

One-pot synthesis of luotonin A and its analogues

MC Tseng, YW Chu, HP Tsai, CM Lin, J Hwang… - Organic …, 2011 - ACS Publications
Starting with inexpensive reagents, a self-directed chemical process with the aid of a single
metal triflate was readily achieved to concomitantly construct quinazoline and …

Iron-catalyzed benzannulation reactions of 2-alkylbenzaldehydes and alkynes leading to naphthalene derivatives

S Zhu, Y Xiao, Z Guo, H Jiang - Organic letters, 2013 - ACS Publications
An efficient and practical method for the synthesis of naphthalene derivatives via Fe (III)-
catalyzed benzannulation of 2-(2-oxoethyl)-benzaldehydes and alkynes has been …

Intermolecular Dehydrative [4 + 2] Aza-Annulation of N-Arylamides with Alkenes: A Direct and Divergent Entrance to Aza-Heterocycles

YH Huang, SR Wang, DP Wu, PQ Huang - Organic letters, 2019 - ACS Publications
We disclose that following activation with trifluoromethanesulfonyl anhydride, secondary N-
arylamides undergo smooth intermolecular dehydrative [4+ 2] aza-annulation with alkenes …

Pd-Catalyzed Branching Cyclizations of Enediyne-Imides toward Furo[2,3-b]pyridines

Z Li, F Ling, D Cheng, C Ma - Organic letters, 2014 - ACS Publications
The convergent synthesis of a class of enediyne-imides as well as their palladium-catalyzed
branching cyclizations, which can be accomplished in two ways leading to a set of …

[PDF][PDF] The Hendrickson 'POP'reagent and analogues thereof: Synthesis, structure, and application in organic synthesis

Z Moussa - Arkivoc, 2012 - academia.edu
This comprehensive review discusses the synthesis, structure, and application of the
Hendrickson 'POP'reagent and its analogues in organic synthesis. Specifically, the review …

Theoretical analysis of lactone and carboxylate forms of camptothecin in aqueous solution: Electronic states, absorption spectra, and hydration

VV Kostjukov - Journal of Molecular Liquids, 2021 - Elsevier
The vibronic absorption spectra of the camptothecin drug in an aqueous solution have been
calculated for the first time. The calculations were carried out by the TD-DFT method. It was …

A dual removable activating group enabled the Povarov reaction of N-arylalanine esters: Synthesis of quinoline-4-carboxylate esters

X Jia, S Lü, Y Yuan, X Zhang, L Zhang… - Organic & Biomolecular …, 2017 - pubs.rsc.org
A dual removable activating group enabled Povarov reaction of N-arylalanine esters was
reported. N-Arylalanine ester was utilized as the sole carbon source to generate N-arylimine …