Molecules from Side Reactions II
"Molecules from Side Reactions II" is the second edition of the Special Issue "Molecules from Side Reactions". Both the Special Issues belong to the section "Organic Synthesis" of the journal Molbank (ISSN 1422-8599). "Molecules from Side Reactions II" showcas...
I tiakina i:
| Ētahi atu kaituhi: | , |
|---|---|
| Hōputu: | Tāhiko Wāhanga pukapuka |
| Reo: | Ingarihi |
| I whakaputaina: |
Basel
MDPI - Multidisciplinary Digital Publishing Institute
2023
|
| Ngā marau: | |
| Urunga tuihono: | DOAB: download the publication DOAB: description of the publication |
| Ngā Tūtohu: |
Tāpirihia he Tūtohu
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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MARC
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| 100 | 1 | |a D'Errico, Stefano |4 edt | |
| 700 | 1 | |a Guaragna, Annalisa |4 edt | |
| 700 | 1 | |a D'Errico, Stefano |4 oth | |
| 700 | 1 | |a Guaragna, Annalisa |4 oth | |
| 245 | 1 | 0 | |a Molecules from Side Reactions II |
| 260 | |a Basel |b MDPI - Multidisciplinary Digital Publishing Institute |c 2023 | ||
| 300 | |a 1 electronic resource (136 p.) | ||
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| 520 | |a "Molecules from Side Reactions II" is the second edition of the Special Issue "Molecules from Side Reactions". Both the Special Issues belong to the section "Organic Synthesis" of the journal Molbank (ISSN 1422-8599). "Molecules from Side Reactions II" showcases brief papers whose main topic is the synthesis and characterization of molecules obtained from unexpected and/or unpredictable synthetic routes. This Special Issue was revealed to be an important discussion forum for the dissemination of multidisciplinary research results. | ||
| 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 | |
| 650 | 7 | |a Chemistry |2 bicssc | |
| 650 | 7 | |a Organic chemistry |2 bicssc | |
| 653 | |a oxoammonium salt | ||
| 653 | |a dehydrogenation | ||
| 653 | |a phenol | ||
| 653 | |a recyclable | ||
| 653 | |a ketone | ||
| 653 | |a pyridazinethione | ||
| 653 | |a spiro[cycloalkane]pyridazine | ||
| 653 | |a hydrazine | ||
| 653 | |a acetone | ||
| 653 | |a Schiff base | ||
| 653 | |a phthalides | ||
| 653 | |a isobenzofuranones | ||
| 653 | |a Fischer indole synthesis | ||
| 653 | |a Claisen-Schmidt reaction | ||
| 653 | |a Witkop reaction | ||
| 653 | |a glycosyl monomer | ||
| 653 | |a acryloylation | ||
| 653 | |a acrylamide | ||
| 653 | |a glycopolymer | ||
| 653 | |a bivalent ligand | ||
| 653 | |a oxazole | ||
| 653 | |a iminium | ||
| 653 | |a unexpected product | ||
| 653 | |a copper cyanide | ||
| 653 | |a network | ||
| 653 | |a cuprophilic | ||
| 653 | |a soft resin | ||
| 653 | |a lupulone-indazole | ||
| 653 | |a NMR Spectroscopy | ||
| 653 | |a solvent-free | ||
| 653 | |a cADPR | ||
| 653 | |a nucleosides | ||
| 653 | |a nucleotides | ||
| 653 | |a inosine | ||
| 653 | |a alkylation | ||
| 653 | |a calcium mobilization | ||
| 653 | |a ryanodine receptor | ||
| 653 | |a primary cortical neurons | ||
| 653 | |a phthalazine | ||
| 653 | |a chlorination | ||
| 653 | |a side product | ||
| 653 | |a phosphonic dichloride | ||
| 653 | |a P. falciparum | ||
| 653 | |a HepG2 | ||
| 653 | |a 19β,28-Epoxy-18α-olean-3β-ol-2-furoate | ||
| 653 | |a betulin | ||
| 653 | |a allobetulin | ||
| 653 | |a iodine | ||
| 653 | |a 2-furoyl chloride | ||
| 653 | |a esterification | ||
| 653 | |a 1,4-naphthodioxane | ||
| 653 | |a dioxane ring opening | ||
| 653 | |a Corey-Chaykovsky epoxidation | ||
| 653 | |a Corey-Chaykovsky byproducts | ||
| 653 | |a 2,6-difluorobenzamide | ||
| 653 | |a FtsZ inhibitors | ||
| 653 | |a nucleophilic aromatic substitution | ||
| 653 | |a adamantane | ||
| 653 | |a thiohydantoin | ||
| 653 | |a by-product | ||
| 653 | |a X-ray structure | ||
| 653 | |a alkyl-BIAN | ||
| 653 | |a picolylamine | ||
| 653 | |a manganese | ||
| 653 | |a condensation reaction | ||
| 653 | |a acenaphthenequinone | ||
| 653 | |a enamine esters | ||
| 653 | |a microwave | ||
| 653 | |a antifungals | ||
| 653 | |a Fusarium oxysporum | ||
| 653 | |a triazol-3-one | ||
| 653 | |a reduction | ||
| 653 | |a heterocyclic ketone | ||
| 653 | |a S-alkylation | ||
| 653 | |a disalicylaldehyde | ||
| 653 | |a trioxabicyclo[3.3.1]nonadiene | ||
| 653 | |a quaternary ammonium salts | ||
| 653 | |a α-carbon benzylation | ||
| 653 | |a N-benzylation | ||
| 653 | |a n/a | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/8170 |7 0 |z DOAB: download the publication |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/128706 |7 0 |z DOAB: description of the publication |