Recent advances in the enantioselective 1, 3-dipolar cycloaddition of azomethine ylides and dipolarophiles

B Bdiri, BJ Zhao, ZM Zhou - Tetrahedron: Asymmetry, 2017 - Elsevier
The synthesis of diastereo-and enantiopure heterocyclic molecules via catalytic asymmetric
1, 3-dipolar cycloaddition reaction between azomethine ylides, generated in situ from α …

Catalytic asymmetric arylation of α-aryl-α-diazoacetates with aniline derivatives

B Xu, ML Li, XD Zuo, SF Zhu… - Journal of the American …, 2015 - ACS Publications
The asymmetric arylation of diazo compounds with aniline derivatives cooperatively
catalyzed by an achiral dirhodium complex and a chiral spiro phosphoric acid is reported …

Electrochemical oxidation of haematoxylin at poly (alanine) modified carbon paste electrode: A cyclic voltammetric study

KV Harisha, BEK Swamy, PS Ganesh… - Journal of …, 2019 - Elsevier
Electrochemical oxidation of haematoxylin (HX), a bioactive bis-catechol molecule was
studied at poly (alanine) modified carbon paste electrode (CPE) by using cyclic voltammetric …

Cyclization of η3-Benzylpalladium Intermediates Derived from Carbene Insertion

ES Gutman, V Arredondo, DL Van Vranken - Organic letters, 2014 - ACS Publications
Migratory insertion of benzylidene carbene ligands into arylpalladium (II) species generates
η3-benzylpalladium intermediates that can cyclize to generate five-and six-membered rings …

[PDF][PDF] Molecular docking of secondary metabolites from Indonesian marine and terrestrial organisms targeting SARS-CoV-2 ACE-2, M pro, and PL pro receptors

G Syahputra, N Gustini, B Bustanussalam… - …, 2021 - pharmacia.pensoft.net
With the uncontrolled spread of severe acute respiratory syndrome coronavirus 2 (SARS-
CoV-2), development and distribution of antiviral drugs and vaccines have gained …

Diastereoselective Synthesis of Cyclopenta[c]chromanones via Pd0-Catalyzed [3+2] Cycloaddition

K Biswas, S Malik, V Ganesh - The Journal of Organic Chemistry, 2024 - ACS Publications
A straightforward method for synthesizing cyclopenta [c] chromanones is demonstrated. The
strategy involves a [3+ 2] cycloaddition of VCPs and activated coumarins under Pd …

[HTML][HTML] Tricyclic flavonoids with 1, 3-dithiolium substructure

LG Bahrin, PG Jones, H Hopf - Beilstein Journal of Organic …, 2012 - beilstein-journals.org
The synthesis of new 3-dithiocarbamic flavonoids has been accomplished by the reaction of
the corresponding 2-hydroxyaryl dithiocarbamates with aminals. These flavonoids were …

[3+2] Annulation of 2-substituted 3-nitro-2H-chromenes with mercaptoacetaldehyde: stereoselective synthesis of tetrahydro-4H-thieno[3,2-c]chromen-3-ols

AY Barkov, IA Kochnev, NS Simonov… - Chemistry of …, 2021 - Springer
A diastereoselective method was developed for the synthesis of 4-trifluoromethyl-and 4-
phenyl-substituted 3a-nitro-2, 3, 3a, 9b-tetrahydro-4 H-thieno [3, 2-c] chromen-3-ols having …

Stereoselective Convergent Synthesis of Tetrahydro-5H-benzo[c]fluorene via Nine-Membered Ring-Closing Metathesis and Transannular Acid-Mediated Cyclization …

A Lekky, T Ruengsatra, S Ruchirawat… - The Journal of Organic …, 2019 - ACS Publications
The diene methyl ethers or acetates, constructed from the Li–Br exchange/addition reactions
of 2-vinylbenzaldehydes and 2-(but-3-en-1-yl) bromoarenes followed by etherification or …

Design and synthesis of a hybrid framework of indanone and chromane: total synthesis of a homoisoflavanoid, brazilane

J Kim, I Kim - Organic & Biomolecular Chemistry, 2018 - pubs.rsc.org
A chemical backbone of tetracyclic homoisoflavanoid natural products such as brazilin
inspired us to design a new chemical scaffold, 6a, 11b-dihydroindeno [2, 1-c] chromen-7 …