A long-range tautomeric effect on a new Schiff isoniazid analogue, evidenced by NMR study and X-ray crystallography-Reference-Cited by-同舟云学术

A long-range tautomeric effect on a new Schiff isoniazid analogue, evidenced by NMR study and X-ray crystallography

Published:2018 Issue:17 Volume:42 Page:14459-14468
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Tănase Constantin I.¹²³^ORCID,Drăghici Constantin⁴⁵³,Shova Sergiu⁶⁷³^ORCID,Hanganu Anamaria⁴⁵³^ORCID,Gal Emese⁸⁹¹⁰³^ORCID,Munteanu Cristian V. A.¹¹¹²³^ORCID

Affiliation:

1. National Institute for Chemical-Pharmaceutical Research and Development

2. Bucharest-3

3. Romania

4. Organic Chemistry Center “C.D.Nenitescu”

5. 060023 Bucharest

6. Institute of Macromolecular Chemistry “Petru Poni”

7. 700478 Iasi

8. Babes-Bolyai University

9. Faculty of Chemistry and Chemical Engineering

10. Cluj-Napoca

11. Romanian Academy-Institute of Biochemistry (IBAR)

12. Bucharest

Abstract

Isoniazid analogues were cyclized through acid catalysis by closing a THF ring, as favoured by Baldwin's rules (5-exo-trig).

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ01680A

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4. Lycopladines B–D and lyconadin B, new alkaloids from Lycopodium complanatum

5. Chrotacumines A−D, Chromone Alkaloids from Dysoxylum acutangulum

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