Modern Trends of Organic Chemistry in Russian Universities

AI Konovalov, IS Antipin, VA Burilov… - Russian Journal of …, 2018 - Springer
This review is devoted to the scientific achievements of the departments of organic chemistry
in higher schools of Russia within the past decade.

Synthesis of 2-aminoindolizines by 1, 3-dipolar cycloaddition of pyridinium ylides with electron-deficient ynamides

J Brioche, C Meyer, J Cossy - Organic letters, 2015 - ACS Publications
Electron-deficient ynamides, possessing an ynoate or an ynone moiety, have been
successfully involved for the first time in a 1, 3-dipolar cycloaddition with stabilized …

Domino Knoevenagel condensation/intramolecular aldol cyclization route to diverse indolizines with densely functionalized pyridine units

M Kim, Y Jung, I Kim - The Journal of Organic Chemistry, 2013 - ACS Publications
A highly efficient [4+ 2] annulation route to polysubstituted indolizines is described
employing a domino Knoevenagel condensation/intramolecular aldol cyclization process as …

[PDF][PDF] Современные тенденции органической химии в университетах России

АИ Коновалов, ИС Антипин, ВА Бурилов… - Журнал …, 2018 - researchgate.net
5. Кафедра органической химии Московского государственного университета им. МВ
Ломоносова. 6. Кафедра химии Российского национального исследовательского …

When indolizine meets quinoline: Diversity-oriented synthesis of new polyheterocycles and their optical properties

S Park, DI Kwon, J Lee, I Kim - ACS Combinatorial Science, 2015 - ACS Publications
Fluorescence-based technologies play a pivotal role in various biomedical applications.
Here we report an efficient route to a new class of fluorophores, indolizino [3, 2-c] quinolines …

Cascade synthesis of pyrido [3, 2-a] indolizines by reaction of Kröhnke–Mukaiyama salts with malononitrile dimer

NM Tverdokhleb, GE Khoroshilov, VV Dotsenko - Tetrahedron Letters, 2014 - Elsevier
An efficient protocol for the synthesis of highly functionalized 2-aminoindolizines and pyrido
[3, 2-a] indolizines has been achieved via the reaction of N-RC (O) CH 2-2-chloropyridinium …

C3 functionalization of indolizines via In (III)-catalyzed three-component reaction

Y Jung, I Kim - Organic & Biomolecular Chemistry, 2015 - pubs.rsc.org
C3 functionalization of indolizines via In( iii )-catalyzed three-component reaction - Organic &
Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB01657F Royal Society of …

Facile synthesis of spiro [indane-2, 1′-pyrrolo [2, 1-a] isoquinolines] via three-component reaction of isoquinolinium salts, indane-1, 3-dione, and isatins

XH Wang, CG Yan - Synthesis, 2014 - thieme-connect.com
A series of novel 2′-aryl-2′-(2-oxo-1, 2-dihydro-3H-indol-3-ylidene)-2′, 3′-dihydro-
10b′ H-spiro [indene-2, 1′-pyrrolo [2, 1-a] isoquinoline]-1, 3-diones were efficiently …

Post-Ugi carbocyclization/fragmentation sequence for the synthesis of 6, 7-dihydro-5H-pyrrolo [3, 4-b] pyridin-5-ones

TTT Trang, AA Peshkov, J Jacobs, L Van Meervelt… - Tetrahedron …, 2015 - Elsevier
A two-step one-pot sequence, involving Ugi reaction followed by base-promoted
carbocyclization accompanied by cleavage of the isocyanide-originated amide moiety, has …

Synthesis of 6a, 6b, 13, 13a-tetrahydro-6H-5-oxa-12a-azadibenzo [a, g] fluorene derivatives via cycloaddition reactions of isoquinolinium salts with 3-nitrochromenes

J Fang, CG Yan - Molecular diversity, 2014 - Springer
An efficient and diastereoselective synthetic procedure for functionalized 6a, 6b, 13, 13a-
tetrahydro-6H-5-oxa-12a-azadibenzo a, g fluorene derivatives was successfully developed …