Chemical synthesis of the cardiotonic steroid glycosides and related natural products

B Heasley - Chemistry–A European Journal, 2012 - Wiley Online Library
The active components from the extracts of Digitalis, cardiotonic steroid glycosides, have
been ingested by humans for more than 200 years as a medicinal therapy for heart failure …

Enantioselective Access to 3-Azabicyclo[3.1.0]hexanes by CpxRhIII Catalyzed C–H Activation and Cp*IrIII Transfer Hydrogenation

O Lahtigui, D Forster, C Duchemin, N Cramer - Acs Catalysis, 2022 - ACS Publications
Rigid saturated nitrogen-containing scaffolds such as 3-azabicyclo [3.1. 0] hexanes are very
important and frequently occurring motifs in biologically active compounds. We disclose a …

Highly Diastereoselective Synthesis of Polysubstituted Cyclopropanecarbonitriles via Palladium-Catalyzed Cyanoesterification of Cyclopropenes

C Li, R Yu, SZ Cai, X Fang - Organic Letters, 2023 - ACS Publications
We herein develop a highly diastereoselective synthesis of cyano-substituted cyclopropanes
via palladium-catalyzed direct cyanoesterification of cyclopropenes, which features mild …

Emerging Trends in N‐Tosylhydrazone Mediated Transition‐Metal‐Free Reactions

R Singhal, SP Choudhary, B Malik, M Pilania - ChemistrySelect, 2022 - Wiley Online Library
This review is based on the recent synthetic advancements of N‐tosylhydrazone under
metal‐free conditions for the construction of nitrogen‐containing heterocycles. N …

Cyclopropanation reactions of semi-stabilized and non-stabilized diazo compounds

EMD Allouche, AB Charette - Synthesis, 2019 - thieme-connect.com
The cyclopropane ring is present in a large number of bioactive molecules as its
incorporation often greatly alters their physiochemical properties. The synthesis of such motif …

Palladium-Catalyzed Borylative Cyclization and Cyclopropanation of Terminal Alkyne-Derived Enynes

D Sun, B Zhou, L Liu, X Chen, H Hou, Y Han… - Organic …, 2023 - ACS Publications
Described herein is a palladium-catalyzed borylative cyclization and cyclopropanation of
terminal alkyne-derived enynes, affording borylated bicycles, fused cycles, and bridged …

Asymmetric reductive and alkynylative heck bicyclization of enynes to access conformationally restricted aza [3.1. 0] bicycles

X Huang, MH Nguyen, M Pu, L Zhang… - Angewandte Chemie …, 2020 - Wiley Online Library
Conformationally restricted azabicycles are becoming increasingly important in medicinal
research. Asymmetric Heck bicyclization of enynes proceeds to give medicinally useful aza …

A Modular Approach to the Synthesis of gem-Disubstituted Cyclopropanes

MR Harris, HM Wisniewska, W Jiao, X Wang… - Organic …, 2018 - ACS Publications
A diastereoselective, Pd-catalyzed Suzuki–Miyaura coupling reaction of geminal bis (boryl)
cyclopropanes has been developed. The reaction offers a highly modular approach to the …

[HTML][HTML] Study of Cytotoxicity of Spiro-Fused [3-Azabicyclo [3.1. 0] hexane] oxindoles and Cyclopropa [a] pyrrolizidine-oxindoles Against Tumor Cell Lines

AA Kornev, SV Shmakov, AI Ponyaev, AV Stepakov… - Pharmaceuticals, 2024 - mdpi.com
Background: A series of spiro-fused heterocyclic compounds containing cyclopropa [a]
pyrrolizidine-2, 3′-oxindole and 3-spiro [3-azabicyclo [3.1. 0]-hexane] oxindole frameworks …

Construction of Spiro [3-azabicyclo [3.1. 0] hexanes] via 1, 3-Dipolar Cycloaddition of 1, 2-Diphenylcyclopropenes to Ninhydrin-Derived Azomethine Ylides

S Wang, AS Filatov, SV Lozovskiy, SV Shmakov… - …, 2021 - thieme-connect.com
The multi-component 1, 3-dipolar cycloaddition of ninhydrin, α-amino acids (or peptides),
and cyclopropenes for the synthesis of spirocyclic heterocycles containing both 3-azabicyclo …