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Kondensierte 1.2‐Dithiole, I. Synthese von Thiolutin und verwandten Verbindungen
Author(s) -
Stachel HansDietrich,
Nienaber Juliane,
Zoukas Thomas
Publication year - 1992
Publication title -
liebigs annalen der chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 0170-2041
DOI - 10.1002/jlac.199219920184
Subject(s) - chemistry
Ring‐Fused 1,2‐Dithioles, I. — Synthesis of Thiolutine and Related Compounds The 1,2‐dithiolopyrrole 1 (thiolutine) has been obtained on two different routes. Firstly, by synthesis of the dithiolopyrrole 6a and introduction of the acetamino function into compound 6d by nitration followed by ester saponification and decarboxylation. 6d is also available from 9k by oxidative ring contraction which occurs with simultaneous dealkylation of the benzylamino group. Secondly, by synthesis of the dithiinopyrrole 15b and introduction of the acetamino function into compound 15g by Beckmann rearrangement followed by ring contraction.

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