Crystallization-Induced Diastereoisomer Transformation of Dihydroartemisinic Aldehyde with the Betti Base-Reference-Cited by-同舟云学术

Crystallization-Induced Diastereoisomer Transformation of Dihydroartemisinic Aldehyde with the Betti Base

Published:2020-01-14 Issue:5 Volume:24 Page:850-855
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Zanetti Andrea¹,Chaumont-Olive Pauline¹,Schwertz Geoffrey¹,Nascimento de Oliveira Marllon²,Gomez Fernandez Mario Andrés²,Amara Zacharias²^ORCID,Cossy Janine¹^ORCID

Affiliation:

1. Molecular, Macromolecular Chemistry and Materials, ESPCI Paris/CNRS/PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France

2. Equipe Chimie Moléculaire, Laboratoire de Génomique, Bioinformatique et Chimie Moléculaire (GBCM), EA 7528, Conservatoire national des arts et métiers, HESAM Université, 2 rue Conté, 75003 Paris Cedex 03, France

Funder

Bill and Melinda Gates Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.oprd.9b00481

Reference19 articles.

1. Synthetic biology’s first malaria drug meets market resistance

2. High-level semi-synthetic production of the potent antimalarial artemisinin

3. Semisynthetic Artemisinin, the Chemical Path to Industrial Production

4. Production of amorphadiene in yeast, and its conversion to dihydroartemisinic acid, precursor to the antimalarial agent artemisinin

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