Fujiwara, Kenshu et al. published their research in Tetrahedron Letters in 2007 | CAS: 14204-27-4

2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Recommanded Product: 2-(Phenylthio)isoindoline-1,3-dione

Synthesis of the C8-C20 and C21-C30 segments of pectenotoxin 2 was written by Fujiwara, Kenshu;Aki, Yu-ichi;Yamamoto, Fuyuki;Kawamura, Mariko;Kobayashi, Masanori;Okano, Azusa;Awakura, Daisuke;Shiga, Shunsuke;Murai, Akio;Kawai, Hidetoshi;Suzuki, Takanori. And the article was included in Tetrahedron Letters in 2007.Recommanded Product: 2-(Phenylthio)isoindoline-1,3-dione This article mentions the following:

In this study, we synthesized the C8-C20 and C21-C30 segments, I and II, resp., of the diarrhetic shellfish toxin pectenotoxin 2. The C8-C20 segment I was assembled from a phosphonate, III, corresponding to the C8-C15 segment (prepared from L-malic acid in 19 steps) and an aldehyde, IV, corresponding to the C16-C20 segment (synthesized from 3-methyl-3-butenol in nine steps) by a twelve-step process including the Horner-Wadsworth-Emmons reaction, regio- and stereoselective reduction of the resulting enone, diastereoselective epoxidation, and 5-exo epoxide cleavage forming the C-ring. The C21-C30 segment II was constructed in 13 steps from (S)-glycidol via a route involving E-ring formation by 5-exo epoxide cleavage and stereoselective methylation at C27 by the Evans method. In the experiment, the researchers used many compounds, for example, 2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4Recommanded Product: 2-(Phenylthio)isoindoline-1,3-dione).

2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Recommanded Product: 2-(Phenylthio)isoindoline-1,3-dione

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles