Inter-and intramolecular reactions of epoxides and aziridines with π-nucleophiles
SH Krake, SC Bergmeier - Tetrahedron, 2010 - Elsevier
The synthesis and reactions of epoxides and aziridines has been regularly reviewed. 1 e6
The most typical reaction of both heterocyclic systems is the ring-opening reaction in which a …
The most typical reaction of both heterocyclic systems is the ring-opening reaction in which a …
Efficient synthesis of 3, 3′-mixed bisindoles via lewis acid catalyzed reaction of spiro-epoxyoxindoles and indoles
An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been
developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro …
developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro …
Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey–Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines
A general and direct strategy for the synthesis of chiral spiro-aziridine oxindoles has been
developed via an aza-Corey–Chaykovsky reaction of isatin-derived N-tert-butanesulfinyl …
developed via an aza-Corey–Chaykovsky reaction of isatin-derived N-tert-butanesulfinyl …
Catalyst-free “on-water” regio-and stereospecific ring-opening of spiroaziridine oxindole: enantiopure synthesis of unsymmetrical 3, 3′-bisindoles
A catalyst-free water-mediated regio-and stereospecific ring-opening reaction of nonracemic
spiroaziridine oxindoles and indoles has been developed with retention of configuration …
spiroaziridine oxindoles and indoles has been developed with retention of configuration …
Regioselective Friedel–Crafts Reaction of Electron‐Rich Benzenoid Arenes and Spiroepoxyoxindole at the Spiro‐Centre: Efficient Synthesis of Benzofuroindolines …
Metal triflate‐catalysed intermolecular Friedel–Crafts reactions involving electron‐rich
benzenoid arenes and spiroepoxyoxindoles at the spiro‐centre have been developed for …
benzenoid arenes and spiroepoxyoxindoles at the spiro‐centre have been developed for …
Catalyst-free ring opening of spiroaziridine oxindoles by heteronucleophiles: An approach to the synthesis of enantiopure 3-substituted oxindoles
A simple catalyst-free method was developed for the ring opening of spiroaziridine
oxindoles by three different nucleophiles, namely, amines, thiols, and methanol, to produce …
oxindoles by three different nucleophiles, namely, amines, thiols, and methanol, to produce …
Catalytic Enantioselective Aziridoarylation of Aryl Cinnamyl Ethers toward Synthesis of trans-3-Amino-4-arylchromans
Catalytic enantioselective one-pot aziridoarylation reaction of aryl cinnamyl ethers has been
demonstrated in detail. Combination of suitable copper catalyst and chiral bis-oxazoline …
demonstrated in detail. Combination of suitable copper catalyst and chiral bis-oxazoline …
[PDF][PDF] A catalytic and enantioselective synthesis of trans-2-amino-1-aryltetralins
The bis-oxazoline-copper complex-catalyzed aziridination of alkenes followed by an
intramolecular Friedel–Crafts alkylation of the tethered and in situ generated aziridine …
intramolecular Friedel–Crafts alkylation of the tethered and in situ generated aziridine …
Catalytic asymmetric aminolactonization of 1, 2-disubstituted alkenoic acid esters: Efficient construction of aminolactones with an all-carbon quaternary stereo-centre
Chiral BOX–Cu (OTf) 2 catalyzed enantioselective aminolactonization of the tert-butyl ester
of alkenoic acids has been developed via in situ aziridination using PhINNs as the nitrene …
of alkenoic acids has been developed via in situ aziridination using PhINNs as the nitrene …
Catalytic enantioselective synthesis of A-86929, a dopamine D1 agonist
Catalytic enantioselective synthesis of A-86929, a dopamine D1 agonist - Chemical
Communications (RSC Publishing) DOI:10.1039/C1CC10263J Royal Society of Chemistry View …
Communications (RSC Publishing) DOI:10.1039/C1CC10263J Royal Society of Chemistry View …