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A reapraisal of the reaction of quinones with hydrazoic acid

✍ Scribed by G.R. Bedford; G. Jones; B.R. Webster

Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
191 KB
Volume
7
Category
Article
ISSN
0040-4039

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✦ Synopsis

The Schmidt reaction, using concentrated sulphurio acid and hydrasoic acid at O*, as applied to alkyl substituted quinones has been the subject of recent studies (1), Folkers & a. come to the conclusion that in the case of quinones such aa h and Ib the products are exclusively of type IIa and IIb.

πŸ“œ SIMILAR VOLUMES

The reaction of decaborane with hydrazoi
The reaction of decaborane with hydrazoic acid: A novel access to azaboranes
✍ J. MΓΌller; P. Paetzold; R. Boese πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 454 KB

The reaction of BfoH12(SMe2)2 (1) with HN3 yields arachno-BfoHf AN3)(NH2) (2), a product with a p N H 2 group. Compound 2 can be hydrolysed to give the known arachno-B9Hf3(NH3) (3). nido-NB9Hf ,(N3) (4) is formed from 2 by a deprotonationlprotonation sequence. The azaborane nido-NBfd13 (5) is a prod