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ISSN:
1523-7060
eISSN:
1523-7052
Disciplines
(Field of Science):
- biomedical engineering (Engineering and Technology)
- materials engineering (Engineering and Technology)
- medical biology (Medical and Health Sciences )
- pharmacology and pharmacy (Medical and Health Sciences )
- agriculture and horticulture (Agricultural sciences)
- food and nutrition technology (Agricultural sciences)
- biotechnology (Natural sciences)
- biological sciences (Natural sciences)
- chemical sciences (Natural sciences)
(Field of Science)
Ministry points: Help
| Year | Points | List |
|---|---|---|
| Year 2024 | 140 | Ministry scored journals list 2024 |
| Year | Points | List |
|---|---|---|
| 2024 | 140 | Ministry scored journals list 2024 |
| 2023 | 140 | Ministry Scored Journals List |
| 2022 | 140 | Ministry Scored Journals List 2019-2022 |
| 2021 | 140 | Ministry Scored Journals List 2019-2022 |
| 2020 | 140 | Ministry Scored Journals List 2019-2022 |
| 2019 | 140 | Ministry Scored Journals List 2019-2022 |
| 2018 | 45 | A |
| 2017 | 45 | A |
| 2016 | 45 | A |
| 2015 | 40 | A |
| 2014 | 40 | A |
| 2013 | 40 | A |
| 2012 | 40 | A |
| 2011 | 40 | A |
| 2010 | 32 | A |
Model:
Hybrid
Points CiteScore:
| Year | Points |
|---|---|
| Year 2023 | 9.3 |
| Year | Points |
|---|---|
| 2023 | 9.3 |
| 2022 | 10.3 |
| 2021 | 10.4 |
| 2020 | 10.2 |
| 2019 | 10.4 |
| 2018 | 10.9 |
| 2017 | 11.6 |
| 2016 | 11.6 |
| 2015 | 11.3 |
| 2014 | 11.2 |
| 2013 | 10.7 |
| 2012 | 9.8 |
| 2011 | 9.2 |
Impact Factor:
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Sherpa Romeo:
Papers published in journal
Filters
total: 4
Catalog Journals
Year 2022
Year 2019
-
Enantiopure C1-Cyclotriveratrylene with a Reversed Spatial Arrangement of the Substituents
Publication -
Magnesiate-Utilized/Benzyne-Mediated Approach to Indenopyridones from 2-Pyridones: An Attempt To Synthesize the Indenopyridine Core of Haouamine
Publication
Year 2012
-
Helicity Discrimination in Diaryl Dichalcogenides Generateded by Inclusion Complexation with Chiral Hosts
PublicationNiektóre z molekuł pozbawione centrum stereogenicznego mogą przyjmować chiralną konformację na skutek wewnętrznej rotacji wzdłuż odpowiedniego wiązania. Do grupy tej należą badane przez nas diarylodichalogenki; diarylodisiarczki, diarylodiselenki i diaryloditellurki. Niska bariera rotacji wokół wiązania chalogen-chalogen skutkuje szybką racemizacją molekuł tych związków w roztworze i uniemożliwia badanie czynności optycznej. Wykazaliśmy,...
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