A Concise Total Synthesis of 7-Substituted Eudistomin Analogs

Ryoichi      Ando; Ge      Li; Ji      Song; Wensheng      Liao; Rujian      Ma; Shu-Hui      Chen; Zuozhong      Peng

doi:10.2174/157017806777828448

Abstract

We report herein an optimized practical synthesis of three novel 7-substituted eudistomin analogs (1-3). The total syntheses of these complex tetracyclic molecules were completed in 22 steps from the requisite 7-substituted indoles.

Keywords: demethylation, diasteroselectivity, Pictet-Spengler cyclization, total Synthesis, Eudistomin analogs

« Previous Next »

Rights & Permissions Print Cite

Letters in Organic Chemistry

Title: A Concise Total Synthesis of 7-Substituted Eudistomin Analogs

Volume: 3 Issue: 6

Author(s): Ryoichi Ando, Ge Li, Ji Song, Wensheng Liao, Rujian Ma, Shu-Hui Chen and Zuozhong Peng

Affiliation:

Keywords: demethylation, diasteroselectivity, Pictet-Spengler cyclization, total Synthesis, Eudistomin analogs

Abstract: We report herein an optimized practical synthesis of three novel 7-substituted eudistomin analogs (1-3). The total syntheses of these complex tetracyclic molecules were completed in 22 steps from the requisite 7-substituted indoles.

Export Options

Export File:

RIS (for EndNote, Reference Manager, ProCite)

BibTeX

Text

Content:

Citation Only

Citation and Abstract

About this article

Cite this article as:

Ando Ryoichi, Li Ge, Song Ji, Liao Wensheng, Ma Rujian, Chen Shu-Hui and Peng Zuozhong, A Concise Total Synthesis of 7-Substituted Eudistomin Analogs, Letters in Organic Chemistry 2006; 3 (6) . https://dx.doi.org/10.2174/157017806777828448