ScholarLens Back to search
1989•ChemInformRequires access

ChemInform Abstract: Chemistry of the Pyrrolo(3,4‐c)pyrido(2,3‐d)pyrimidine System. Synthesis of 6,7‐Dihydropyrrolo(3,4‐c)pyrido(2,3‐d)pyrimidines, a Novel Ring System with Potential Biological Interest.

Ting‐Li Su, Kyoichi A. Watanabe

Open publisher page 0 citations

Abstract

Abstract The key step in the synthesis of the pyrrolopyridopyrimidine (V) is the thermally induced cyclization of the 5‐aminomethyl‐6‐acetoxymethylpyridopyrimidine derivative (IV).

About this research paper

What this paper is about

Abstract The key step in the synthesis of the pyrrolopyridopyrimidine (V) is the thermally induced cyclization of the 5‐aminomethyl‐6‐acetoxymethylpyridopyrimidine derivative (IV).

Why it matters

A significance statement is not available in the OpenAlex record.

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

Abstract The key step in the synthesis of the pyrrolopyridopyrimidine (V) is the thermally induced cyclization of the 5‐aminomethyl‐6‐acetoxymethylpyridopyrimidine derivative (IV).

Key concepts: Chemistry, Pyrimidine, Ring (chemistry), Derivative (finance), Stereochemistry, D-1, Combinatorial chemistry, Organic chemistry

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Chemistry of the Pyrrolo(3,4‐c)pyrido(2,3‐d)pyrimidine System. Synthesis of 6,7‐Dihydropyrrolo(3,4‐c)pyrido(2,3‐d)pyrimidines, a Novel Ring System with Potential Biological Interest. — Research Paper | ScholarLens