Photoreactions of Isoindoline-1-thiones with Alkenes: Unusual Formation of Tricyclic Isoindolines

DOI: 10.1021/jo00040a049

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Journal of Organic Chemistry p. 4000 - 4005 (1992)

Update date:2022-08-04

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Authors:

Nishio, Takehiko

Okuda, Norikazu

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Article abstract of DOI:10.1021/jo00040a049

Photochemical cycloaddition reactions of cyclic thioamides and alkenes have been examined.Irradiation of 2-arylisoindoline-1-thiones 1 in the presence of alkenes 2 gave the unexpected tricyclic isoindolines 3-18.The formation of tricyclic isoindolines can

Full text of DOI:10.1021/jo00040a049

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Article Doi

Photoreactions of Isoindoline-1-thiones with Alkenes: Unusual Formation of Tricyclic Isoindolines

DOI: 10.1021/jo00040a049

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00040a049

Full text of DOI:10.1021/jo00040a049

Products guided by the article

R&D Labs maybe for 141663-70-9

Relevant to this article

Evaluation of (4-aminobutyloxy)quinolines as a novel class of antifungal agents

Synthesis of farnesol analogues containing triazoles in place of isoprenes through 'click chemistry'

N?H-Type Excited-State Proton Transfer in Compounds Possessing a Seven-Membered-Ring Intramolecular Hydrogen Bond

Inhibition of nitric oxide and prostaglandin E2 production by pyrrolylated-chalcones: Synthesis, biological activity, crystal structure analysis, and molecular docking studies

Nickel(ii)-catalyzed tandem C(sp2)-H bond activation and annulation of arenes with gem-dibromoalkenes

Mechanistic studies on the metal-free activation of dihydrogen by antiaromatic pentarylboroles

Nickel(ii)-catalyzed tandem C(sp²)-H bond activation and annulation of arenes with gem-dibromoalkenes