ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.

Abstract Treatment of the urethanes (I) with bromine leads to mixtures of the adducts (II) (spectroscopically identified, but not isolated), the oxazolidinones (III) [obtained only in the cases (IIIa)‐(IIIf)], and the tetrahydrooxazinones(IV) [obtained in all cases except (IVd)].

Bibliographic Details
Published in:Chemischer Informationsdienst
Main Authors: MUEHLSTAEDT, M. +, OLK, B., WIDERA, R.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1986
Subjects:
Carbonic acid
Online Access:http://dx.doi.org/10.1002/chin.198645134
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id crwiley:10.1002/chin.198645134
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spelling crwiley:10.1002/chin.198645134 2024-06-02T08:05:10+00:00 ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones. MUEHLSTAEDT, M. + OLK, B. WIDERA, R. 1986 http://dx.doi.org/10.1002/chin.198645134 http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198645134 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198645134 https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.198645134 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Chemischer Informationsdienst volume 17, issue 45 ISSN 0009-2975 2199-2924 journal-article 1986 crwiley https://doi.org/10.1002/chin.198645134 2024-05-03T11:26:40Z Abstract Treatment of the urethanes (I) with bromine leads to mixtures of the adducts (II) (spectroscopically identified, but not isolated), the oxazolidinones (III) [obtained only in the cases (IIIa)‐(IIIf)], and the tetrahydrooxazinones(IV) [obtained in all cases except (IVd)]. Article in Journal/Newspaper Carbonic acid Wiley Online Library Chemischer Informationsdienst 17 45
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Treatment of the urethanes (I) with bromine leads to mixtures of the adducts (II) (spectroscopically identified, but not isolated), the oxazolidinones (III) [obtained only in the cases (IIIa)‐(IIIf)], and the tetrahydrooxazinones(IV) [obtained in all cases except (IVd)].
format Article in Journal/Newspaper
author MUEHLSTAEDT, M. +
OLK, B.
WIDERA, R.
spellingShingle MUEHLSTAEDT, M. +
OLK, B.
WIDERA, R.
ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
author_facet MUEHLSTAEDT, M. +
OLK, B.
WIDERA, R.
author_sort MUEHLSTAEDT, M. +
title ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
title_short ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
title_full ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
title_fullStr ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
title_full_unstemmed ChemInform Abstract: Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. Part 9. Regiochemistry of Electrophilic Cyclofunctionalization of β,γ‐Unsaturated Carbamic Acid Esters with Bromine ‐ Synthesis of Oxazolidine‐2‐ones and Tetrahydro‐2H‐1,3‐oxazine‐2‐ones.
title_sort cheminform abstract: cyclization reactions of β,γ‐unsaturated derivatives of carbonic acid. part 9. regiochemistry of electrophilic cyclofunctionalization of β,γ‐unsaturated carbamic acid esters with bromine ‐ synthesis of oxazolidine‐2‐ones and tetrahydro‐2h‐1,3‐oxazine‐2‐ones.
publisher Wiley
publishDate 1986
url http://dx.doi.org/10.1002/chin.198645134
http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198645134
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198645134
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.198645134
genre Carbonic acid
genre_facet Carbonic acid
op_source Chemischer Informationsdienst
volume 17, issue 45
ISSN 0009-2975 2199-2924
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/chin.198645134
container_title Chemischer Informationsdienst
container_volume 17
container_issue 45
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