One pot synthesis of α,β-epoxy ketones by oxidative coupling of methyl arenes with cinnamic acids involving C(sp3)―H activation and decarboxylative strategy
A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive.
Gespeichert in:
| Autor*in: |
Singh, Rahul [verfasserIn] |
|---|
| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2017 |
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| Schlagwörter: |
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| Umfang: |
5 |
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| Übergeordnetes Werk: |
Enthalten in: Therapeutic Advances in Pediatric Multiple Sclerosis - 2013, the international journal for the rapid publication of full original research papers and critical reviews in organic chemistry, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:73 ; year:2017 ; number:21 ; day:25 ; month:05 ; pages:3074-3078 ; extent:5 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.tet.2017.04.025 |
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ELV035653892 |
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| 520 | |a A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive. | ||
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10.1016/j.tet.2017.04.025 doi GBVA2017001000011.pica (DE-627)ELV035653892 (ELSEVIER)S0040-4020(17)30397-6 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 150 VZ LING DE-30 fid 77.00 bkl Singh, Rahul verfasserin aut One pot synthesis of α,β-epoxy ketones by oxidative coupling of methyl arenes with cinnamic acids involving C(sp3)―H activation and decarboxylative strategy 2017 5 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive. CH activation Elsevier Decarboxylation Elsevier Epoxidation Elsevier Carboxylic acids Elsevier Oxidative coupling Elsevier Kumar, Saurabh oth Singh, Krishna Nand oth Enthalten in Elsevier Science Therapeutic Advances in Pediatric Multiple Sclerosis 2013 the international journal for the rapid publication of full original research papers and critical reviews in organic chemistry Amsterdam [u.a.] (DE-627)ELV011938943 volume:73 year:2017 number:21 day:25 month:05 pages:3074-3078 extent:5 https://doi.org/10.1016/j.tet.2017.04.025 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-LING 77.00 Psychologie: Allgemeines VZ AR 73 2017 21 25 0525 3074-3078 5 045F 540 |
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one pot synthesis of α,β-epoxy ketones by oxidative coupling of methyl arenes with cinnamic acids involving c(sp3)―h activation and decarboxylative strategy |
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One pot synthesis of α,β-epoxy ketones by oxidative coupling of methyl arenes with cinnamic acids involving C(sp3)―H activation and decarboxylative strategy |
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A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive. |
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A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive. |
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A new one pot oxidative coupling of methyl arenes with cinnamic acids has been developed for the synthesis of α,β-epoxy ketones using MnO2/TBHP combination. The process involves a co-existing C(sp3)―H activation and decarboxylation under aqueous medium, which makes it practical and attractive. |
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One pot synthesis of α,β-epoxy ketones by oxidative coupling of methyl arenes with cinnamic acids involving C(sp3)―H activation and decarboxylative strategy |
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