Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters

Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters

[2+3] Dipolar cycloadditions of aromatic nitrile oxides to abietic acid esters were investigated. The reactions showed complete site selectivity and regioselectivity, while the stereoselectivity depended on the structures of the dipolarophiles.

Bibliographic Details
Main Authors: Gucma Mirosław, Gołębiewski Marek W., Żelechowski Krzysztof, Krawczyk Maria
Format: Article
Language:English
Published: Serbian Chemical Society 2019-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
dipolar cycloaddition
abietates
site selectivity
nmr spectroscopy
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2019/0352-51391900018G.pdf
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spelling doaj-9b1e053fe2854f90a94fb681ed16d2bb2020-11-25T03:00:19ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51391820-74212019-01-0184101073108110.2298/JSC180517018G0352-51391900018GStudies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid estersGucma Mirosław0Gołębiewski Marek W.1Żelechowski Krzysztof2Krawczyk Maria3Institute of Industrial Organic Chemistry, Warsaw, PolandInstitute of Industrial Organic Chemistry, Warsaw, PolandInstitute of Industrial Organic Chemistry, Warsaw, PolandInstitute of Industrial Organic Chemistry, Warsaw, Poland[2+3] Dipolar cycloadditions of aromatic nitrile oxides to abietic acid esters were investigated. The reactions showed complete site selectivity and regioselectivity, while the stereoselectivity depended on the structures of the dipolarophiles.http://www.doiserbia.nb.rs/img/doi/0352-5139/2019/0352-51391900018G.pdfdipolar cycloadditionabietatessite selectivitynmr spectroscopy
collection DOAJ
language English
format Article
sources DOAJ
author Gucma Mirosław
Gołębiewski Marek W.
Żelechowski Krzysztof
Krawczyk Maria
spellingShingle Gucma Mirosław
Gołębiewski Marek W.
Żelechowski Krzysztof
Krawczyk Maria
Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
Journal of the Serbian Chemical Society
dipolar cycloaddition
abietates
site selectivity
nmr spectroscopy
author_facet Gucma Mirosław
Gołębiewski Marek W.
Żelechowski Krzysztof
Krawczyk Maria
author_sort Gucma Mirosław
title Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
title_short Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
title_full Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
title_fullStr Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
title_full_unstemmed Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
title_sort studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters
publisher Serbian Chemical Society
series Journal of the Serbian Chemical Society
issn 0352-5139
1820-7421
publishDate 2019-01-01
description [2+3] Dipolar cycloadditions of aromatic nitrile oxides to abietic acid esters were investigated. The reactions showed complete site selectivity and regioselectivity, while the stereoselectivity depended on the structures of the dipolarophiles.
topic dipolar cycloaddition
abietates
site selectivity
nmr spectroscopy
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2019/0352-51391900018G.pdf
work_keys_str_mv AT gucmamirosław studiesonthe23cycloadditionreactionofnitrileoxidestoabieticacidesters
AT gołebiewskimarekw studiesonthe23cycloadditionreactionofnitrileoxidestoabieticacidesters
AT zelechowskikrzysztof studiesonthe23cycloadditionreactionofnitrileoxidestoabieticacidesters
AT krawczykmaria studiesonthe23cycloadditionreactionofnitrileoxidestoabieticacidesters
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