Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten

Acylation of N‐(2, 6‐Dimethylphenyl)‐α‐alanine Methylester with sp‐hybridized Carbonic Acid Derivatives . The title compound 5 reacts with isocyanates and isothiocyanates to yield the substituted imidazolidinones 7 and 8 , respectively, whereas with chlorosulfonyl isocyanate the open chained urea 9...

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Published in:Journal für Praktische Chemie
Main Author: Martin, D.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1991
Subjects:
Carbonic acid
Online Access:http://dx.doi.org/10.1002/prac.19913330210
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spelling crwiley:10.1002/prac.19913330210 2024-06-02T08:05:10+00:00 Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten Martin, D. 1991 http://dx.doi.org/10.1002/prac.19913330210 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fprac.19913330210 https://onlinelibrary.wiley.com/doi/pdf/10.1002/prac.19913330210 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal für Praktische Chemie volume 333, issue 2, page 261-266 ISSN 0021-8383 journal-article 1991 crwiley https://doi.org/10.1002/prac.19913330210 2024-05-03T12:03:27Z Acylation of N‐(2, 6‐Dimethylphenyl)‐α‐alanine Methylester with sp‐hybridized Carbonic Acid Derivatives . The title compound 5 reacts with isocyanates and isothiocyanates to yield the substituted imidazolidinones 7 and 8 , respectively, whereas with chlorosulfonyl isocyanate the open chained urea 9 is formed. Cyanation of 5 takes place with phenyl cyanate and cyanogene bromide. Consecutive reactions of the primary products are described. Article in Journal/Newspaper Carbonic acid Wiley Online Library Journal für Praktische Chemie 333 2 261 266
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Acylation of N‐(2, 6‐Dimethylphenyl)‐α‐alanine Methylester with sp‐hybridized Carbonic Acid Derivatives . The title compound 5 reacts with isocyanates and isothiocyanates to yield the substituted imidazolidinones 7 and 8 , respectively, whereas with chlorosulfonyl isocyanate the open chained urea 9 is formed. Cyanation of 5 takes place with phenyl cyanate and cyanogene bromide. Consecutive reactions of the primary products are described.
format Article in Journal/Newspaper
author Martin, D.
spellingShingle Martin, D.
Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
author_facet Martin, D.
author_sort Martin, D.
title Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
title_short Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
title_full Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
title_fullStr Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
title_full_unstemmed Acyllerung von N‐(2, 6‐Dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten Kohlensäurederlvaten
title_sort acyllerung von n‐(2, 6‐dimethylphenyl)‐α‐alaninmethylester mit sp‐hybridisierten kohlensäurederlvaten
publisher Wiley
publishDate 1991
url http://dx.doi.org/10.1002/prac.19913330210
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fprac.19913330210
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prac.19913330210
genre Carbonic acid
genre_facet Carbonic acid
op_source Journal für Praktische Chemie
volume 333, issue 2, page 261-266
ISSN 0021-8383
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/prac.19913330210
container_title Journal für Praktische Chemie
container_volume 333
container_issue 2
container_start_page 261
op_container_end_page 266
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