2014ChemInformRequires access

ChemInform Abstract: Convenient Primary Amidation of N‐Protected Phenylglycine and Dipeptides Without Racemization or Epimerization.

Takuya Noguchi, Seunghee Jung, Nobuyuki Imai

Open publisher page 0 citations

Abstract

Abstract The activation and amidation step proceeds at low temperature, thus avoiding racemization of the products.

About this research paper

What this paper is about

Abstract The activation and amidation step proceeds at low temperature, thus avoiding racemization of the products.

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 activation and amidation step proceeds at low temperature, thus avoiding racemization of the products.

Key concepts: Chemistry, Racemization, Epimer, Primary (astronomy), Organic chemistry, Combinatorial chemistry, Stereochemistry, Physics

Related papers

Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Convenient Primary Amidation of N‐Protected Phenylglycine and Dipeptides Without Racemization or Epimerization. — Research Paper | ScholarLens