ScholarLens Back to search
2007•Organic LettersRequires access

Synthesis of the C1−C12 Fragment of the Tedanolides. Aldol−Non-Aldol Aldol Approach

Michael E. Jung, Dongwon Yoo

Open publisher page 19 citations

Abstract

The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C1-C12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1.

About this research paper

What this paper is about

The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C1-C12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1.

Why it matters

OpenAlex reports 19 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The combination of highly stereoselective non-aldol aldol and aldol processes allows the preparation of the completely protected C1-C12 fragment 2 of the novel macrocyclic cytotoxic agent tedanolide 1.

Key concepts: Aldol reaction, Chemistry, Fragment (logic), Stereoselectivity, Stereochemistry, Aldol condensation, Organic chemistry, Catalysis

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
Synthesis of the C1−C12 Fragment of the Tedanolides. Aldol−Non-Aldol Aldol Approach — Research Paper | ScholarLens