A facile method for synthesis of three carbon-homologated carboxylic acid by regioselective ring-opening of β-propiolactones with organocopper reagents-Reference-Cited by-同舟云学术

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A facile method for synthesis of three carbon-homologated carboxylic acid by regioselective ring-opening of β-propiolactones with organocopper reagents

Published:1989-01 Issue:2 Volume:45 Page:403-412
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kawashima Masatoshi,Sato Toshio,Fujisawa Tamotsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference56 articles.

1. Chemistry and spectroscopy in strongly acidic solutions. Part XIX: Behaviour of α,α-dimethyl-β-propiolactone and hydroxypivalic acid in hydrogen fluoride-boron trifluoride solution

2. Stereospecific synthesis of - and -1 alkoxy-1,3-butadienes

3. Syntheses of hydroxy ketones from lactones

4. Reaction of Organometallic Compounds with Propiolactone

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1. Ultrafast Solid-Phase Oxidation of Aldehydes to Carboxylic Acids by Atmosphseric Plasma Treatment;ACS Omega;2024-06-06

2. Rings of Power: Enzymatic Routes to β-Lactones;Comprehensive Natural Products III;2020

3. Organocatalysis applied to the ring-opening polymerization of β-lactones: A brief overview;Journal of Polymer Science Part A: Polymer Chemistry;2019-01-13

4. Organocopper reagents;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-20

5. Organocopper reagents;Fieser and Fieser's Reagents for Organic Synthesis;2017-02-20

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