Stereoselective Shi-type epoxidation with 3-oxo-4,6-<i>O</i>-benzylidene pyranoside catalysts: unveiling the role of carbohydrate skeletons-Reference-Cited by-同舟云学术

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Stereoselective Shi-type epoxidation with 3-oxo-4,6-O-benzylidene pyranoside catalysts: unveiling the role of carbohydrate skeletons

Published:2024 Issue:24 Volume:14 Page:16778-16783
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Imperio Daniela¹^ORCID,Valloni Filippo¹,Caprioglio Diego¹,Minassi Alberto¹^ORCID,Casali Emanuele²^ORCID,Panza Luigi¹^ORCID

Affiliation:

1. Department of Pharmaceutical Sciences, Università del Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy

2. Department of Chemistry, University of Pavia, Viale Taramelli, 12, 27100 Pavia, Italy

Abstract

Sugar-derived chiral ketones are capable of reversing stereoselectivity in Shi-type epoxidation.

Funder

Ministero dell'Istruzione e del Merito

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D4RA03011G

Reference34 articles.

1. Green Chemistry Meets Asymmetric Organocatalysis: A Critical Overview on Catalysts Synthesis

2. Green Asymmetric Organocatalysis

3. Growing Impact of Carbohydrate‐Based Organocatalysts

4. Organocatalysis applied to carbohydrates: from roots to current developments

5. An Efficient Catalytic Asymmetric Epoxidation Method

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