ZIB

Hits per page

hit 1 - 1 | 1 hit

Select All Export

Electronic Resource

Cyansäureester. 25 [1]. Umsetzung von Mercapto-N-heterocyclen mit Arylcyanaten (1978)

Martin, Dieter ; Wenzel, Angelika ; Bacaloglu, Radu

New York, NY : Wiley-Blackwell

Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 677-684

add to mindlist on the mindlist

Details

ISSN: 0021-8383

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Cyanic Acid Esters. 25 The Reaction of Mercapto-N-heterocycles with Aryl CyanatesUnsaturated N-heterocycles containing a cyclic thio urea structure and aryl cyanates (molar ratio 1:2), react to form azolo(1,2-d) (1,2,4)thiadiazoles. This reaction has a wide scope concerning starting materials and gives good yields. Under the same conditions 2-thione-benzthiazolin is transformed to the corresponding disulfide. 4,5-Bis-mercaptomethylene-o-xylene and aryl cyanates give 2,3-dithia-6, 7-dimethyl-tetraline.

Additional Material: 1 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/prac.19783200422

Library	Location	Call Number	Volume/Issue/Year	Availability

Others were also interested in ...

Paper (German National Licenses)

Fulltext

hit 1 - 1 | 1 hit