Organophosphorus Chemistry A New Perspective
The Printed Edition of the Special Issue "Organophosphorus Chemistry: A New Perspective" takes the reader on a journey through the chemistry of organophosphorus compounds. It contains seven original research articles and three reviews covering aspects of recent advances in the synthesis, t...
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| Format: | Electronic Book Chapter |
| Language: | English |
| Published: |
Basel
MDPI - Multidisciplinary Digital Publishing Institute
2023
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| Subjects: | |
| Online Access: | DOAB: download the publication DOAB: description of the publication |
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| 700 | 1 | |a Adamek, Jakub |4 oth | |
| 245 | 1 | 0 | |a Organophosphorus Chemistry |b A New Perspective |
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| 300 | |a 1 electronic resource (248 p.) | ||
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| 520 | |a The Printed Edition of the Special Issue "Organophosphorus Chemistry: A New Perspective" takes the reader on a journey through the chemistry of organophosphorus compounds. It contains seven original research articles and three reviews covering aspects of recent advances in the synthesis, transformation, and properties of P-compounds. | ||
| 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 Physical chemistry |2 bicssc | |
| 653 | |a phosphonium salts | ||
| 653 | |a N-acyliminium cations | ||
| 653 | |a α-amidoalkylation | ||
| 653 | |a α-amidoalkylating agents | ||
| 653 | |a ylides | ||
| 653 | |a Wittig reaction | ||
| 653 | |a α-aminophosphonates | ||
| 653 | |a α-aminophosphinates | ||
| 653 | |a α-aminophosphine oxides | ||
| 653 | |a rare earth elements | ||
| 653 | |a actinoids | ||
| 653 | |a separation | ||
| 653 | |a recovery | ||
| 653 | |a extraction | ||
| 653 | |a precipitation | ||
| 653 | |a α-aminobisphosphonates | ||
| 653 | |a α-ethoxyphosphonates | ||
| 653 | |a N-acylimidates | ||
| 653 | |a Michaelis-Becker reaction | ||
| 653 | |a Michaelis-Arbuzov reaction | ||
| 653 | |a betulin | ||
| 653 | |a triphenylphosphonium cation | ||
| 653 | |a anticancer | ||
| 653 | |a antibacterial activity | ||
| 653 | |a osteoporosis | ||
| 653 | |a bisphosphonates | ||
| 653 | |a zoledronate | ||
| 653 | |a metal phosphonates | ||
| 653 | |a hybrid materials | ||
| 653 | |a controlled release | ||
| 653 | |a MOFs | ||
| 653 | |a strontium | ||
| 653 | |a barium | ||
| 653 | |a acene | ||
| 653 | |a anthracene | ||
| 653 | |a phosphine | ||
| 653 | |a phosphonate | ||
| 653 | |a phosphonium salt | ||
| 653 | |a phosphorane | ||
| 653 | |a phosphate | ||
| 653 | |a diphosphene | ||
| 653 | |a tri-, tetra-, pentacoordinated phosphorus | ||
| 653 | |a properties | ||
| 653 | |a HWE reaction | ||
| 653 | |a Still-Gennari olefination | ||
| 653 | |a Ando olefination | ||
| 653 | |a stereoselective synthesis | ||
| 653 | |a Z-selectivity | ||
| 653 | |a phosphonates | ||
| 653 | |a alkenes | ||
| 653 | |a hexafluoroisopropanol | ||
| 653 | |a C=C bond formation | ||
| 653 | |a Reformatsky reaction | ||
| 653 | |a tetrasubstituted α-aminophosphonates | ||
| 653 | |a aspartic acid | ||
| 653 | |a antiproliferative effect | ||
| 653 | |a diazotization | ||
| 653 | |a carbenium ion | ||
| 653 | |a 1-phosphonoalkylium ion | ||
| 653 | |a substitution reaction | ||
| 653 | |a elimination reaction | ||
| 653 | |a rearrangement | ||
| 653 | |a aminophosphonates | ||
| 653 | |a heteroaromatic | ||
| 653 | |a lithiation | ||
| 653 | |a phosphonylation | ||
| 653 | |a phosphonic acids | ||
| 653 | |a organophosphorus chemistry | ||
| 653 | |a P-containing drugs | ||
| 653 | |a n/a | ||
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| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/112447 |7 0 |z DOAB: description of the publication |