Hydrazidine, V. Synthese und Reaktionen aromatischer und aliphatischer Hydrazidine und derenN1-substituierter Derivate
✍ Scribed by Neunhoeffer, Hans ;Karafiat, Ute ;Köhler, Gernot ;Sowa, Birgit
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 885 KB
- Volume
- 1992
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
✦ Synopsis
Hydrazidines, V. — Synthesis and Reactions of Aromatic and Aliphatic Hydrazidines and Their N^1^‐Substituted Derivatives
Aromatic hydrazidines 3 have been synthetized by reaction of aromatic orthocarboxylates 4 with tert‐butyl carbazate (5) and reaction of the protected hydrazidines 7 with HCl/methanol or HBr/acetic acid. Aliphatic N^1^‐methylhydrazidines 8 have been prepared by methylation of bis (tert‐butoxycarbonyl)‐hydrazidines 7 and deprotection with HBr/acetic acid. Aromatic N^1^‐methylhydrazidines 8 have been obtained by methylation of N^1^‐methyl(thiohydrazides) 11, reaction of 12 with tert‐butyl carbazate (5) and deprotection of 13 with HCl/methanol. — Attempts to remove both protecting groups in N^1^‐alkyl‐N^2^,N^4^‐bis
📜 SIMILAR VOLUMES
Hydrochloric acid and hydrobromic acid react with α‐mono‐ and α, α‐disubstituted β‐lactones under ring cleavage leading unequivocally to the corresponding α‐mono‐ or α, α‐disubstituted β‐halogenopropionic acids. These products are interesting starting materials for the preparation of new compounds a