A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds
Publication type: Journal Article
Publication date: 2011-04-06
scimago Q2
wos Q2
SJR: 0.600
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
21584300
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
2-Aminobenzothiazoles are readily synthesised from anilines, sulfur monochloride and isocyanides. The key step consists of an iodine-catalysed insertion of isocyanides into the S-S bond of hydrolysed Herz salts, with concomitant extrusion of sulfur monoxide.
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15
Total citations:
15
Citations from 2024:
2
(13.34%)
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MLA
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GOST
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Neo A. G., Carrillo R. M., Marcos C. F. A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds // Organic and Biomolecular Chemistry. 2011. Vol. 9. No. 13. p. 4850.
GOST all authors (up to 50)
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Neo A. G., Carrillo R. M., Marcos C. F. A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds // Organic and Biomolecular Chemistry. 2011. Vol. 9. No. 13. p. 4850.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c1ob05398a
UR - https://doi.org/10.1039/c1ob05398a
TI - A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds
T2 - Organic and Biomolecular Chemistry
AU - Neo, Ana G
AU - Carrillo, Rosa M
AU - Marcos, Carlos F
PY - 2011
DA - 2011/04/06
PB - Royal Society of Chemistry (RSC)
SP - 4850
IS - 13
VL - 9
PMID - 21584300
SN - 1477-0520
SN - 1477-0539
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2011_Neo,
author = {Ana G Neo and Rosa M Carrillo and Carlos F Marcos},
title = {A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds},
journal = {Organic and Biomolecular Chemistry},
year = {2011},
volume = {9},
publisher = {Royal Society of Chemistry (RSC)},
month = {apr},
url = {https://doi.org/10.1039/c1ob05398a},
number = {13},
pages = {4850},
doi = {10.1039/c1ob05398a}
}
Cite this
MLA
Copy
Neo, Ana G., et al. “A straightforward synthesis of 2-aminobenzothiazoles from Herz compounds.” Organic and Biomolecular Chemistry, vol. 9, no. 13, Apr. 2011, p. 4850. https://doi.org/10.1039/c1ob05398a.