1987ChemInformRequires access

ChemInform Abstract: Acyclic Stereoselection. Part 40. Steric Effects, as Well as σ*‐Orbital Energies, Are Important in Diastereoface Differentiation in Additions to Chiral Aldehydes.

Eric P. Lodge, Clayton H. Heathcock

Open publisher page 0 citations

Abstract

Abstract Two series of aldehydes (V) and (VII) are prepared as shown in the scheme except for (VIId) which is available from commercial sources.

About this research paper

What this paper is about

Abstract Two series of aldehydes (V) and (VII) are prepared as shown in the scheme except for (VIId) which is available from commercial sources.

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 Two series of aldehydes (V) and (VII) are prepared as shown in the scheme except for (VIId) which is available from commercial sources.

Key concepts: Chemistry, Steric effects, Computational chemistry, Series (stratigraphy), Organic chemistry, Stereochemistry, Biology, Paleontology

Related papers

Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Acyclic Stereoselection. Part 40. Steric Effects, as Well as σ*‐Orbital Energies, Are Important in Diastereoface Differentiation in Additions to Chiral Aldehydes. — Research Paper | ScholarLens