Iron(III) chloride as mild catalyst for the dearomatizing cyclization of N-acylindoles
| dc.contributor.author | Zhang, Jingyu | |
| dc.contributor.author | Li, Jing | |
| dc.contributor.author | Ward, Jas S | |
| dc.contributor.author | Truong, Khai-Nghi | |
| dc.contributor.author | Rissanen, Kari | |
| dc.contributor.author | Albrecht, Markus | |
| dc.date.accessioned | 2020-09-07T07:04:06Z | |
| dc.date.available | 2020-09-07T07:04:06Z | |
| dc.date.issued | 2020 | |
| dc.identifier.citation | Zhang, J., Li, J., Ward, J. S., Truong, K.-N., Rissanen, K., & Albrecht, M. (2020). Iron(III) chloride as mild catalyst for the dearomatizing cyclization of N-acylindoles. <i>Journal of Organic Chemistry</i>, <i>85</i>(19), 12160-12174. <a href="https://doi.org/10.1021/acs.joc.0c01373" target="_blank">https://doi.org/10.1021/acs.joc.0c01373</a> | |
| dc.identifier.other | CONVID_41899758 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/71659 | |
| dc.description.abstract | A catalytic approach for the preparation of indolines by dearomatizing cyclization is presented. FeCl3 acts as a catalyst to afford tetracyclic 5a,6-dihydro-12H-indolo[2,1-b][1,3]benzoxazin-12-ones in good yields. The cyclization also proceeds with tosylamides forming C-N bonds in 53 % yield. | en |
| dc.format.mimetype | application/pdf | |
| dc.language | eng | |
| dc.language.iso | eng | |
| dc.publisher | American Chemical Society (ACS) | |
| dc.relation.ispartofseries | Journal of Organic Chemistry | |
| dc.rights | In Copyright | |
| dc.subject.other | indoliini | |
| dc.title | Iron(III) chloride as mild catalyst for the dearomatizing cyclization of N-acylindoles | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-202009075768 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 12160-12174 | |
| dc.relation.issn | 0022-3263 | |
| dc.relation.numberinseries | 19 | |
| dc.relation.volume | 85 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © 2020 American Chemical Society | |
| dc.rights.accesslevel | openAccess | fi |
| dc.subject.yso | katalyysi | |
| dc.subject.yso | orgaaninen kemia | |
| dc.subject.yso | katalyytit | |
| dc.subject.yso | kemialliset yhdisteet | |
| dc.format.content | fulltext | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p8704 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p11902 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p15480 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p324 | |
| dc.rights.url | http://rightsstatements.org/page/InC/1.0/?language=en | |
| dc.relation.doi | 10.1021/acs.joc.0c01373 | |
| jyx.fundinginformation | Jingyu Zhang gratefully acknowledges support by the Chinese Scholarship Council. | |
| dc.type.okm | A1 |
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