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An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles

Тип публикацииJournal Article
Дата публикации2013-10-30
scimago Q2
wos Q3
БС2
SJR0.482
CiteScore3.8
Impact factor2.1
ISSN18605397
Organic Chemistry
Краткое описание

This review which is the second in this series summarises the most common synthetic routes as applied to the preparation of many modern pharmaceutical compounds categorised as containing a six-membered heterocyclic ring. The reported examples are based on the top retailing drug molecules combining synthetic information from both scientific journals and the wider patent literature. It is hoped that this compilation, in combination with the previously published review on five-membered rings, will form a comprehensive foundation and reference source for individuals interested in medicinal, synthetic and preparative chemistry.

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ГОСТ |
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Baumann M. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles // Beilstein Journal of Organic Chemistry. 2013. Vol. 9. pp. 2265-2319.
ГОСТ со всеми авторами (до 50) Скопировать
Baumann M. An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles // Beilstein Journal of Organic Chemistry. 2013. Vol. 9. pp. 2265-2319.
RIS |
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TY - JOUR
DO - 10.3762/bjoc.9.265
UR - https://doi.org/10.3762/bjoc.9.265
TI - An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles
T2 - Beilstein Journal of Organic Chemistry
AU - Baumann, Marcus
PY - 2013
DA - 2013/10/30
PB - Beilstein-Institut
SP - 2265-2319
VL - 9
PMID - 24204439
SN - 1860-5397
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2013_Baumann,
author = {Marcus Baumann},
title = {An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles},
journal = {Beilstein Journal of Organic Chemistry},
year = {2013},
volume = {9},
publisher = {Beilstein-Institut},
month = {oct},
url = {https://doi.org/10.3762/bjoc.9.265},
pages = {2265--2319},
doi = {10.3762/bjoc.9.265}
}