New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method for indole synthesis

W Sun, WAT Raimbach, LD Elliott… - Chemical …, 2022 - pubs.rsc.org
New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method
for indole synthesis - Chemical Communications (RSC Publishing) DOI:10.1039/D1CC05700F …

[引用][C] Heteroatom directed photoarylation synthesis of functionalized indolines

AG Schultz, CK Sha - Tetrahedron, 1980 - Elsevier
HETEROATOM DIRECTED PHOTOARYLATION Page 1 Trrmhtdmn Vol. 36, pp. 1757 to
1761 Pergamon Press Ltd., 1980. Printed in Great Britain HETEROATOM DIRECTED …

Heteroatom-directed photoarylation: synthesis of indoles and 3-hydroxyindolines

AG Schultz, WK Hagmann - Journal of the Chemical Society, Chemical …, 1976 - pubs.rsc.org
Heteroatorn -directed Photoarylation : Synthesis of Indoles and 3 -Hydroxyindolines Page 1
726 JCS CHEM. COMM., 1976 Heteroatorn -directed Photoarylation : Synthesis of Indoles and …

Visible‐Light‐Promoted Iminyl‐Radical Formation from Acyl Oximes: A Unified Approach to Pyridines, Quinolines, and Phenanthridines

H Jiang, X An, K Tong, T Zheng… - Angewandte Chemie …, 2015 - Wiley Online Library
A unified strategy involving visible‐light‐induced iminyl‐radical formation has been
established for the construction of pyridines, quinolines, and phenanthridines from acyl …

Visible Light‐Induced Aerobic Oxyamidation of Indoles: A Photocatalytic Strategy for the Preparation of Tetrahydro‐5H‐indolo[2,3‐b]quinolinols

J An, YQ Zou, QQ Yang, Q Wang… - Advanced Synthesis & …, 2013 - Wiley Online Library
A visible light‐induced, aerobic oxyamidation reaction of indoles, using air as the sole
oxidant, has been developed. This process serves as a photocatalytic strategy to generate …

Photocatalytic aerobic oxidation/semipinacol rearrangement sequence: a concise route to the core of pseudoindoxyl alkaloids

W Ding, QQ Zhou, J Xuan, TR Li, LQ Lu, WJ Xiao - Tetrahedron Letters, 2014 - Elsevier
A visible light-induced photocatalytic aerobic oxidation/semipinacol rearrangement has
been successfully developed. This methodology allows for efficient conversion of a wide …

Visible light mediated azomethine ylide formation—photoredox catalyzed [3+ 2] cycloadditions

M Rueping, D Leonori, T Poisson - Chemical Communications, 2011 - pubs.rsc.org
Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions -
Chemical Communications (RSC Publishing) DOI:10.1039/C1CC13660G Royal Society of …

A Visible‐Light‐Mediated Oxidative CN Bond Formation/Aromatization Cascade: Photocatalytic Preparation of N‐Arylindoles

S Maity, N Zheng - Angewandte Chemie International Edition, 2012 - Wiley Online Library
Indoles are heterocyclic motifs that are embedded in a large number of bioactive natural
products and pharmaceuticals.[1] As such, the search for sustainable and more efficient …

Photocatalytic synthesis of polycyclic indolones

T Saget, B König - Chemistry–A European Journal, 2020 - Wiley Online Library
In this work, a photocatalytic strategy for a rapid and modular access to polycyclic indolones
starting from readily available indoles is reported. This strategy relies on the use of redox …

Photochemical transormations. XXXVIII. Nonoxidative photocyclization of N-aryl enamines. A facile synthetic entry to trans-hexahydrocarbazoles

OL Chapman, GL Eian, A Bloom… - Journal of the American …, 1971 - ACS Publications
Nonoxidative photocyclization of A-aryl enamines gives indolinesin good yield. The reaction
provides the first useful synthetic entry to tra/w-hexahydrocarbazoles and is useful for …