Stereoselective Construction of Entire Diastereomeric Stereotetrads Based on an Asymmetric Morita-Baylis-Hillman Reaction-Reference-Cited by-同舟云学术

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Stereoselective Construction of Entire Diastereomeric Stereotetrads Based on an Asymmetric Morita-Baylis-Hillman Reaction

Published:2017-05-18 Issue:19 Volume:2017 Page:2719-2729
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Yoshimura Hikaru¹,Ishihara Jun¹,Hatakeyama Susumi²

Affiliation:

1. Graduate School of Biomedical Sciences; Nagasaki University; 1-14 Bunkyo-machi 852-8521 Nagasaki Japan

2. Medical Innovation Center; Nagasaki University; 1-14 Bunkyo-machi 852-8521 Nagasaki Japan

Funder

Japan Society for the Promotion of Science

Ministry of Education, Culture, Sports, Science and Technology-JAPAN

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference53 articles.

1. Polyketide biosynthesis: a millennium review

2. Polyketide stereotetrads in natural products

3. Boron Enolate Chemistry toward the Syntheses of Polyketide Stereotetrads

4. A New Role for Polyketides

5. Eine neue Rolle für Polyketide

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1. Iterative Homologation of Boronic Esters: Assembly Line Synthesis;Homologation Reactions;2023-05-26

2. Highly Efficient Asymmetric Morita–Baylis–Hillman Reaction Promoted by Chiral Aziridine-Phosphines;Catalysts;2022-03-31

3. The Application of Biocatalysis in the Preparation and Resolution of Morita‐Baylis‐Hillman Adducts and Their Derivatives;ChemBioChem;2021-12-06

4. Total Synthesis of Enantioenriched Quinine;Journal of Synthetic Organic Chemistry, Japan;2021-02-01

5. Fascinated by Natural Product Synthesis;Journal of Synthetic Organic Chemistry, Japan;2020-10-01

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