Synthesis 1990; 1990(3): 237-242
DOI: 10.1055/s-1990-26842
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Oxokohlenstoffe und verwandte Verbindungen; 14. Mitteilung.1 Chemie der Semiquadratsäure: Reaktive Semiquadratsäure-Abkömmlinge und deren Umsetzung mit N-Nucleophilen

Arthur H. Schmidt* , Michael Debo, Bernhard Wehner
  • *Abteilung für Organische Chemie und Biochemie, Fachhochschule Fresenius, Kapellenstraße 11-15, D-6200 Wiesbaden Federal Republic of Germany
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
17. September 2002 (online)

Oxocarbons and Related Compounds; Part 14. The Chemistry of Semisquaric Acid: Highly Reactive Semisquaric Acid Derivatives and Their Reactions with N-Nucleophiles Starting from semisquaric acid (1), the semisquaric esters 6a-d and semisquaric chloride (7) were prepared. Reaction of 6c or 7 with amines as well as the method of mixed anhydrides, starting from 1, afforded the semisquaric amides 10a-n (Methods A, B, C, respectively). The semisquaric amides 10g,h,i were also obtained by the reaction of semisquaric chloride (7) with the trimethylsilylamines 11a-c (Method D); 10h was furthermore prepared by the DCC-method (Method E). The reaction of butyl squarate (6c) with hydrazines and N-alkylhydroxylamines afforded the semisquaric hydrazides 13a-d and the semisquaric hydroxylamides 15a-c, respectively.