Efficient synthesis of α,β-dichlorinated ketones from α,β-dichlorinated Weinreb amides through a simple work-up procedure
Author:
Affiliation:
1. Division of Environmental Materials Science, Graduate School of Environmental Science, Hokkaido University, N10W5 Sapporo 060-0810, Japan
2. Chemistry Department, Universitas Islam Indonesia, Sleman, Yogyakarta, Indonesia
Abstract
Funder
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01379C
Reference33 articles.
1. N-methoxy-n-methylamides as effective acylating agents
2. Direct Conversion of N-Methoxy-N-methylamides (Weinreb Amides) to Ketones via a Nonclassical Wittig Reaction
3. Vinyl Weinreb amides: a versatile alternative to vinyl ketone substrates for the Heck arylation
4. Highly efficient synthesis of functionalized α-oxyketones via Weinreb amides homologation with α-oxygenated organolithiums
5. Synthesis of Enantiomerically Pure β-Hydroxy Ketones via β-Keto Weinreb Amides by a Condensation/Asymmetric-Hydrogenation/Acylation Sequence
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