ScholarLens Back to search
2016•ChemInformRequires access

ChemInform Abstract: Synthesis of 2,6‐trans‐ and 3,3,6‐Trisubstituted Tetrahydropyran‐4‐ones from Maitland—Japp Derived 2H‐Dihydropyran‐4‐ones: A Total Synthesis of Diospongin B.

Paul A. Clarke, Nadiah Mad Nasir, Philip B. Sellars, Alejandra M. Peter, Connor A. Lawson, James L. Burroughs

Open publisher page 0 citations

Abstract

Abstract A modification of the Maitland—Japp reaction utilizing orthoamides provides access to a range of 6‐substituted dihydropyranones.

About this research paper

What this paper is about

Abstract A modification of the Maitland—Japp reaction utilizing orthoamides provides access to a range of 6‐substituted dihydropyranones.

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 A modification of the Maitland—Japp reaction utilizing orthoamides provides access to a range of 6‐substituted dihydropyranones.

Key concepts: Chemistry, Tetrahydropyran, Dihydropyran, Total synthesis, Stereochemistry, Organic chemistry, Ring (chemistry), Catalysis

Related papers

Related paper 1Related paper 2
Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Synthesis of 2,6‐trans‐ and 3,3,6‐Trisubstituted Tetrahydropyran‐4‐ones from Maitland—Japp Derived 2H‐Dihydropyran‐4‐ones: A Total Synthesis of Diospongin B. — Research Paper | ScholarLens