Heteroatorn -directed Photoarylation : Synthesis of Indoles and 3 -Hydroxyindolines Page 1
726 JCS CHEM. COMM., 1976 Heteroatorn -directed Photoarylation : Synthesis of Indoles and …

HETEROATOM DIRECTED PHOTOARYLATION Page 1 Trrmhtdmn Vol. 36, pp. 1757 to
1761 Pergamon Press Ltd., 1980. Printed in Great Britain HETEROATOM DIRECTED …

1, 2-Fused indoles and pyrroles were prepared via an efficient intramolecular photoaddition
reaction of 1-(ω-alkenyl)-2-haloindole-3-carbaldehydes and 1-(ω-alkenyl)-2-chloropyrrole-3 …

Pyrroles are present in many natural products which exhibit interesting biological activity.
Since pyrrole ring system is a" n-excessive" heteroaromatic that electrophiles substitute …

The N-(2-bromophenyl)-, N-(2-bromobenzyl)-, and N-(2-bromophenethyl)-derivatives (3) of 3-
aminocyclohex-2-enones and 1, 2, 3, 3a, 4, 5-hexahydro-1-(2-halogeno-4, 5 …

A one‐pot, tandem synthesis of cyclic ethers is obtained by addition of photogenerated
phenyl cations to hydroxyalkenes. Thus, 2‐(or 3‐) phenyl‐substituted tetrahydrofurans were …

New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method
for indole synthesis - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC05700F …

In our continuing studies on the photoreaction of halopyridines with aromatic cornpounds,
we have recently reported that the photoreaction of 2-halopyridine (halogen; Cl, Br, I) and …

The intramolecular addition reactions of phototransient species generated upon heteroatom
directed photoarylation were investigated. Novel temperature effects were observed for both …

A series of 2-aryloxyenones 5a-u is prepared by reaction of the appropriate phenol with
isophorone epoxide and base in refluxing tetrahydrofuran-hexamethylphosphoramide …