ISSN:
1615-4150
eISSN:
1615-4169
Disciplines
(Field of Science):
- biomedical engineering (Engineering and Technology)
- chemical engineering (Engineering and Technology)
- medical biology (Medical and Health Sciences )
- pharmacology and pharmacy (Medical and Health 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 | 45 | A |
2014 | 45 | A |
2013 | 45 | A |
2012 | 45 | A |
2011 | 45 | A |
2010 | 32 | A |
Model:
Hybrid
Points CiteScore:
Year | Points |
---|---|
Year 2023 | 9.4 |
Year | Points |
---|---|
2023 | 9.4 |
2022 | 10.5 |
2021 | 10.9 |
2020 | 9.9 |
2019 | 9.3 |
2018 | 8.6 |
2017 | 9.1 |
2016 | 9.6 |
2015 | 10.4 |
2014 | 9.7 |
2013 | 9.4 |
2012 | 9.4 |
2011 | 9 |
Impact Factor:
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Sherpa Romeo:
Papers published in journal
Filters
total: 1
Catalog Journals
Year 2020
-
Diastereoselective Synthesis of Z‐Alkenyl Disulfides from α‐Thiophosphorylated Ketones and Thiosulfonates
PublicationWe developed a simple and efficient method for the synthesis of functionalized unsymmetrical Z‐alkenyl disulfides under mild conditions in moderate to good yields. The designed method is based on the reaction of α‐thiophosphorylated carbonyl compounds with thiotosylates in the presence of a base. The developed method allows the preparation of unsymmetrical Z‐alkenyl disulfides bearing additional hydroxy, carboxy, or ester functionalities
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