Synthesis of New Type Stable Heterotriene. Conjugated Dienic Thioketone

DOI: 10.1246/cl.1988.1029

Source and publish data:

Chemistry Letters p. 1029 - 1032 (1988)

Update date:2022-09-26

Topics:

Authors:

Karakasa, Takayuki

Moriyama, Satoshi

Motoki, Shinichi

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Article abstract of DOI:10.1246/cl.1988.1029

2-Phenyl-3-thiobenzoyl-5,6-dihydrobenzo-2H-thiochromene was synthesized in 4 steps from 2-(phenylthio)methylene-1-tetralone.The thione reacted as a heterodiene with norbornene to give the corresponding <4+2>cycloadduct.

Full text of DOI:10.1246/cl.1988.1029

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Article Doi

Synthesis of New Type Stable Heterotriene. Conjugated Dienic Thioketone

DOI: 10.1246/cl.1988.1029

Source and publish data:

Authors:

Article abstract of DOI:10.1246/cl.1988.1029

Full text of DOI:10.1246/cl.1988.1029

Products guided by the article

R&D Labs maybe for 118210-61-0

Relevant to this article

Enantioselective syntheses of morpholines and their homologues via S N2-type ring opening of aziridines and azetidines with haloalcohols

Development and application of a new general method for the asymmetric synthesis of (E)-(2-En-3-ynyl)-amines

Surprising isomer preference on IrIII, favoring facile H-C(sp3) bond cleavage

Aminophosphine palladium pincer complexes for Suzuki and Heck reactions

Intramolecular <3+2> Cycloaddition Reactions in the Indole Series "The Nitrile Oxide Route to the Ergot Alkaloids". 1. Chanoclavine I

Gold-catalyzed one-pot cascade construction of highly functionalized pyrrolo[1,2-a]quinolin-1(2H)-ones

Enantioselective syntheses of morpholines and their homologues via S _N2-type ring opening of aziridines and azetidines with haloalcohols

Surprising isomer preference on Ir^III, favoring facile H-C(sp³) bond cleavage