89313-76-8

Upstream product

• 5388-42-1 N-phenylphthalimidine 
• 18167-15-2 3-hydroxy-2-phenylisoindolin-1-one 
• 33125-69-8 (±)-3-(phenylamino)isobenzofuran-1(3H)-one 
• 496-12-8 isoindoline 
• 108-86-1 bromobenzene 
• 19375-67-8 2-phenylisoindoline 
• 62-53-3 aniline 
• 91-13-4 α,α'-dibromo-o-xylene 
• 119-67-5 o-carboxybenzaldehyde 
• 6940-49-4 3-Bromophthalide 

Downstream Products

• 141663-69-6 10,11,11-Trimethyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene 
• 141663-68-5 10,10,11,11-Tetramethyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene 
• 141663-73-2 (1R,8R,11R)-11-Methyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene-11-carboxylic acid methyl ester 
• 141663-73-2 (1R,8R,11S)-11-Methyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene-11-carboxylic acid methyl ester 
• 141663-71-0 (1S,8S,11R)-11-Methyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene-11-carbonitrile 
• 141663-71-0 (1S,8S,11S)-11-Methyl-12-phenyl-9-thia-12-aza-tricyclo[6.3.1.0^2,7]dodeca-2,4,6-triene-11-carbonitrile 
• 93273-28-0 C₂₇H₂₄N₂O₃S 
• 141636-32-0 1-(1',1',2'-trimethyl-2'-propenyl)-phenylisoindoline 
• 19375-67-8 2-phenylisoindoline 

Relevant academic research and scientific papers

Solvent-driven C(sp3)-H thiocarbonylation of benzylamine derivatives under catalyst-free conditions

Due to the particularity of the thiocarbonyl group (C S bond), only limited C(sp3)-H thiocarbonylation methods, especially efficient and convenient methods, have been developed for the synthesis of thioamides. Inspired by the “solvent-specifici

Visible-Light-Mediated C(sp3)–H Thiocarbonylation for Thiolactam Preparation with Potassium Sulfide

We report herein a protocol for thiolactam preparation with potassium sulfide via visible-light-mediated C(sp3)–H thiocarbonylation, in which polysulfide dianions and radical anions generated from potassium sulfide were the key active species. A variety of thiolactams were straightforward established under mild conditions. Moreover, it was successfully applied to structural modification of tetrahydroberberine.

Preparation of 3-Hydroxyindolin-1-ones and o-Acylbenzamides. A Study of Ring-Chain Tautomerism

3-Hydroxyisoindolinones (ring form) as well as their chain tautomers, o-acylbenzamides, were prepared from the reactions of 3-benzalphthalide 1, 3-halophthalides 3, and o-acylbenzoic acids 6 or their esters 7 with amines 2, and those of phthalimides 4 wit

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

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

Reaction of 3-Hydroxyisoindolin-1-ones with Lawesson Reagent. Synthesis of Isoindoline-1-thiones

Treatment of 3-hydroxyisoindolin-1-ones 1 with Lawesson reagent gave isoindoline-1-thiones 2, by direct thionation and reductive elimination of hydroxy group, in good yields.

1-ETHYLTHIO-2R-ISOINDOLES. AN EXAMPLE OF NONSYNCHRONOUS ADDITION IN THE DIELS-ALDER REACTION

The previously unknown 1-ethylthio-2R-isoindoles have been obtained by modifying the corresponding isoindol-1-ones.The reaction of these isoindoles with N-arylmaleimide derivatives has been investigated.A rare case of nonsynchronous addition in the Diels-