2005Bopuxue zazhiOpen access

Structural Confirmation of a Derivative of 6, 7; 12, 21-Didehydroerythromycin A by ~(13)C NMR DEPT Technique

Lei Ping-sheng

Open full text 0 citations

Abstract

The derivatives of (9S)-12-methyleneerythromycin A, compound (5) and (6), were obtained by elimination reaction between thionyl chloride and corresponding 2′-O, 4″-O-dibenzoyl-(9S)-9-O, 11-O-isopropylerythromycin A The structure of (6) was established using ~13C-NMR-DEPT spectroscopy

About this research paper

What this paper is about

The derivatives of (9S)-12-methyleneerythromycin A, compound (5) and (6), were obtained by elimination reaction between thionyl chloride and corresponding 2′-O, 4″-O-dibenzoyl-(9S)-9-O, 11-O-isopropylerythromycin A The structure of (6) was established using ~13C-NMR-DEPT spectroscopy

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

The derivatives of (9S)-12-methyleneerythromycin A, compound (5) and (6), were obtained by elimination reaction between thionyl chloride and corresponding 2′-O, 4″-O-dibenzoyl-(9S)-9-O, 11-O-isopropylerythromycin A The structure of (6) was established using ~13C-NMR-DEPT spectroscopy

Key concepts: DEPT, Thionyl chloride, Chemistry, Carbon-13 NMR, Nuclear magnetic resonance spectroscopy, Fluorine-19 NMR, Derivative (finance), Nuclear magnetic resonance

Related papers

Back to paper searchBrowse research topicsOriginal source
Structural Confirmation of a Derivative of 6, 7; 12, 21-Didehydroerythromycin A by ~(13)C NMR DEPT Technique — Research Paper | ScholarLens