Isoxazolidine: a privileged scaffold for organic and medicinal chemistry

M Berthet, T Cheviet, G Dujardin, I Parrot… - Chemical …, 2016 - ACS Publications
The isoxazolidine ring represents one of the privileged structures in medicinal chemistry,
and there have been an increasing number of studies on isoxazolidine and isoxazolidine …

Recent advances in small organic molecules as DNA intercalating agents: Synthesis, activity, and modeling

A Rescifina, C Zagni, MG Varrica, V Pistarà… - European journal of …, 2014 - Elsevier
The interaction of small molecules with DNA plays an essential role in many biological
processes. As DNA is often the target for majority of anticancer and antibiotic drugs, study …

The Nitrosocarbonyl Hetero‐Diels–Alder Reaction as a Useful Tool for Organic Syntheses

BS Bodnar, MJ Miller - Angewandte Chemie International …, 2011 - Wiley Online Library
Organic transformations that result in the formation of multiple covalent bonds within the
same reaction are some of the most powerful tools in synthetic organic chemistry …

Addition of carbon-centered radicals to imines and related compounds

GK Friestad - Tetrahedron, 2001 - Elsevier
Imines (azomethines), iminium salts, and related compounds have been used as
electrophiles for ionic bond constructions (eg in the Mannich reaction) for many years, but …

Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions

PF Vogt, MJ Miller - Tetrahedron, 1998 - Elsevier
The Diels-Alder cycloaddition has become one of the most used and dependable reactions
in all of organic synthesis, t One reason for its popularity is that asynunetric versions of the …

Total Synthesis and Biological Evaluation of Amaryllidaceae Alkaloids:  Narciclasine, ent-7-Deoxypancratistatin, Regioisomer of 7-Deoxypancratistatin, 10b-epi …

T Hudlicky, U Rinner, D Gonzalez… - The Journal of …, 2002 - ACS Publications
Biocatalytic approaches have yielded efficient total syntheses of the major Amaryllidaceae
alkaloids, all based on the key enzymatic dioxygenation of suitable aromatic precursors …

Catalytic enantioselective nitroso Diels–Alder reaction

B Maji, H Yamamoto - Journal of the American Chemical Society, 2015 - ACS Publications
The nitroso Diels–Alder (NDA) reaction is an attractive strategy for the synthesis of 3, 6-
dihydro-1, 2-oxazines and 1-amino-4-hydroxy-2-ene derivatives. Herein we report the Cu (I) …

Diastereoselective synthesis of 1, 1, 3, 3-tetrasubstituted cyclobutanes enabled by cycloaddition of bicyclo [1.1. 0] butanes

M Wang, Y Huang, C Li, P Lu - Organic Chemistry Frontiers, 2022 - pubs.rsc.org
Bicyclo [1.1. 0] butanes (BCBs), a class of highly strained saturated bicyclic carbocycles,
have garnered increasing attention in recent years. Functionalization of BCBs provides an …

Stereoselective syntheses of epothilones A and B via nitrile oxide cycloadditions and related studies

JW Bode, EM Carreira - The Journal of organic chemistry, 2001 - ACS Publications
The expedient and fully stereocontrolled synthesis of epothilones A and B are described.
The routes described make extensive study of nitrile oxide cycloadditions as surrogates for …

Catalytic, highly enantio, and diastereoselective nitroso Diels− Alder reaction

Y Yamamoto, H Yamamoto - Journal of the American Chemical …, 2004 - ACS Publications
This communication presents studies that nitroso Diels− Alder adduct has been furnished in
uniformly high yield and high enantioselectivity using nitrosopyridine as a substrate and …