Synthesis of Oxazoline and Oxazole Derivatives by Hypervalent-Iodine-Mediated Oxidative Cycloaddition Reactions; Synthesis; Vol. 52, iss. 16
| Parent link: | Synthesis Vol. 52, iss. 16.— 2020.— [P. 2299-2310] |
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| Korporacja: | |
| Kolejni autorzy: | , , , |
| Streszczenie: | Title screen Organohypervalent iodine reagents are widely used for the preparation of various oxazolines, oxazoles, isoxazolines, and isoxazoles. In the formation of these heterocyclic compounds, hypervalent iodine species can serve as the activating reagents for various substrates, as well as the heteroatom donor reagents. In recent research, both chemical and electrochemical approaches toward generation of hypervalent iodine species have been utilized. The in situ generated active species can react with appropriate substrates to give the corresponding heterocyclic products. In this short review, we summarize the hypervalent-iodine-mediated preparation of oxazolines, oxazoles, isoxazolines, and isoxazoles starting from various substrates.1 Introduction 2 Synthesis of Oxazolines 3 Synthesis of Oxazoles 4 Synthesis of Isoxazolines 5 Synthesis of Isoxazoles 6 Conclusion Режим доступа: по договору с организацией-держателем ресурса |
| Język: | angielski |
| Wydane: |
2020
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| Hasła przedmiotowe: | |
| Dostęp online: | https://doi.org/10.1055/s-0040-1707122 |
| Format: | MixedMaterials Elektroniczne Rozdział |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663365 |
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| 200 | 1 | |a Synthesis of Oxazoline and Oxazole Derivatives by Hypervalent-Iodine-Mediated Oxidative Cycloaddition Reactions |f A. Yoshimura, A. Saito, M. S. Yusubov, V. V. Zhdankin | |
| 203 | |a Text |c electronic | ||
| 300 | |a Title screen | ||
| 320 | |a [References: 154 tit.] | ||
| 330 | |a Organohypervalent iodine reagents are widely used for the preparation of various oxazolines, oxazoles, isoxazolines, and isoxazoles. In the formation of these heterocyclic compounds, hypervalent iodine species can serve as the activating reagents for various substrates, as well as the heteroatom donor reagents. In recent research, both chemical and electrochemical approaches toward generation of hypervalent iodine species have been utilized. The in situ generated active species can react with appropriate substrates to give the corresponding heterocyclic products. In this short review, we summarize the hypervalent-iodine-mediated preparation of oxazolines, oxazoles, isoxazolines, and isoxazoles starting from various substrates.1 Introduction 2 Synthesis of Oxazolines 3 Synthesis of Oxazoles 4 Synthesis of Isoxazolines 5 Synthesis of Isoxazoles 6 Conclusion | ||
| 333 | |a Режим доступа: по договору с организацией-держателем ресурса | ||
| 461 | |t Synthesis | ||
| 463 | |t Vol. 52, iss. 16 |v [P. 2299-2310] |d 2020 | ||
| 610 | 1 | |a электронный ресурс | |
| 610 | 1 | |a труды учёных ТПУ | |
| 610 | 1 | |a hypervalent iodine | |
| 610 | 1 | |a oxidative cyclization | |
| 610 | 1 | |a oxidative cycloaddition | |
| 610 | 1 | |a oxazoles | |
| 610 | 1 | |a oxazolines | |
| 610 | 1 | |a isoxazoles | |
| 610 | 1 | |a isoxazolines | |
| 610 | 1 | |a гипервалентный йод | |
| 610 | 1 | |a оксазолы | |
| 610 | 1 | |a изоксазолы | |
| 701 | 1 | |a Yoshimura |b A. |c chemical engineer |c Professor of Tomsk Polytechnic University |f 1981- |g Akira |3 (RuTPU)RU\TPU\pers\39852 |9 21126 | |
| 701 | 1 | |a Saito |b A. |g Akio | |
| 701 | 1 | |a Yusubov |b M. S. |c chemist |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences |f 1961- |g Mekhman Suleiman-Ogly (Suleimanovich) |3 (RuTPU)RU\TPU\pers\31833 | |
| 701 | 1 | |a Zhdankin |b V. V. |c химик |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences |f 1956- |g Viktor Vladimirovich |3 (RuTPU)RU\TPU\pers\35758 | |
| 712 | 0 | 2 | |a Национальный исследовательский Томский политехнический университет |b Исследовательская школа химических и биомедицинских технологий (ИШХБМТ) |c (2017- ) |3 (RuTPU)RU\TPU\col\23537 |
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