Synthesis of Flavonoids or Other Nature-Inspired Small Molecules
This Special Issue aims to provide an updated overview of the flourishing ongoing research activity in the field of the chemistry of natural and nature-inspired compounds. Ten of the submitted articles were accepted for publication after peer-review. Interestingly, the published papers cover a wide...
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| Format: | Book Chapter |
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Basel
MDPI - Multidisciplinary Digital Publishing Institute
2022
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| Online Access: | Get Fullteks DOAB: description of the publication |
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| LEADER | 03303naaaa2200805uu 4500 | ||
|---|---|---|---|
| 001 | doab_20_500_12854_79622 | ||
| 005 | 20220321 | ||
| 020 | |a books978-3-0365-3245-5 | ||
| 020 | |a 9783036532448 | ||
| 020 | |a 9783036532455 | ||
| 024 | 7 | |a 10.3390/books978-3-0365-3245-5 |c doi | |
| 041 | 0 | |a English | |
| 042 | |a dc | ||
| 072 | 7 | |a GP |2 bicssc | |
| 100 | 1 | |a Ribaudo, Giovanni |4 edt | |
| 700 | 1 | |a Ribaudo, Giovanni |4 oth | |
| 245 | 1 | 0 | |a Synthesis of Flavonoids or Other Nature-Inspired Small Molecules |
| 260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2022 | ||
| 300 | |a 1 electronic resource (82 p.) | ||
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a This Special Issue aims to provide an updated overview of the flourishing ongoing research activity in the field of the chemistry of natural and nature-inspired compounds. Ten of the submitted articles were accepted for publication after peer-review. Interestingly, the published papers cover a wide range of chemical reactions, different scaffolds, and several medicinal chemistry applications. Moreover, this Special Issue gathered contributions from all over the world, testifying the international scientific community's interest in this topic. I would like to sincerely thank the MDPI staff, particularly Jade Lu and the editorial team of Molbank. I am particularly grateful to the authors that decided to share the results of their research by contributing their manuscript to this Special Issue, and, of course, to the reviewers for their valuable help. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
| 546 | |a English | ||
| 650 | 7 | |a Research & information: general |2 bicssc | |
| 653 | |a quercetin | ||
| 653 | |a flavonoids | ||
| 653 | |a semi-synthetic | ||
| 653 | |a PDE | ||
| 653 | |a sildenafil | ||
| 653 | |a molecular modeling | ||
| 653 | |a Garcinia porrecta | ||
| 653 | |a Clusiaceae | ||
| 653 | |a xanthone | ||
| 653 | |a Lansium domesticum | ||
| 653 | |a Meliaceae | ||
| 653 | |a MCF-7 | ||
| 653 | |a triterpene onoceranoid | ||
| 653 | |a hydrazone | ||
| 653 | |a (+)-camphor | ||
| 653 | |a valproic acid | ||
| 653 | |a technology | ||
| 653 | |a terpenoid | ||
| 653 | |a anticonvulsant activity | ||
| 653 | |a 1,2,3-triazole | ||
| 653 | |a anticancer | ||
| 653 | |a aminoquinoline | ||
| 653 | |a hybrid compound | ||
| 653 | |a kokosanolide | ||
| 653 | |a tetranortriterpenoid | ||
| 653 | |a C. dichotoma | ||
| 653 | |a antidiabetic | ||
| 653 | |a α-glucosidase | ||
| 653 | |a α-amylase | ||
| 653 | |a docking | ||
| 653 | |a ADMET | ||
| 653 | |a curcumin analog | ||
| 653 | |a organic synthesis | ||
| 653 | |a photophysical properties | ||
| 653 | |a steady-state fluorescence | ||
| 653 | |a DFT calculation | ||
| 653 | |a 7-hydroxy-2H-chromen-2-one | ||
| 653 | |a O-acylation reaction | ||
| 653 | |a coumarin | ||
| 653 | |a lupeol derivative | ||
| 653 | |a benzylidene derivative | ||
| 653 | |a α-glucosidase inhibition | ||
| 653 | |a Oxone® | ||
| 653 | |a n/a | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/5007 |7 0 |z Get Fullteks |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/79622 |7 0 |z DOAB: description of the publication |