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- Publisher Website: 10.1002/anie.201704155
- Scopus: eid_2-s2.0-85021013396
- WOS: WOS:000405308500051
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Article: Dearomative Intramolecular (4+3) Cycloadditions of Arenes with Epoxy and Aziridinyl Enolsilanes
| Title | Dearomative Intramolecular (4+3) Cycloadditions of Arenes with Epoxy and Aziridinyl Enolsilanes |
|---|---|
| Authors | |
| Keywords | arenes cycloaddition dearomatization heterocycles synthetic methods |
| Issue Date | 2017 |
| Publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home |
| Citation | Angewandte Chemie (International Edition), 2017, v. 56, p. 8879-8882 How to Cite? |
| Abstract | An intramolecular (4+3) cycloaddition of epoxy and aziridinyl enolsilanes with benzene, naphthalene, and anthracene derivatives is reported. Highly functionalized polycyclic alcohols and amines are generated under relatively mild reaction conditions with yields up to 89 %. Optically enriched cycloadducts are obtained from cycloadditions of enantiomerically pure epoxides and aziridines. |
| Persistent Identifier | http://hdl.handle.net/10722/243004 |
| ISSN | 2021 Impact Factor: 16.823 2020 SCImago Journal Rankings: 5.831 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | LING, J | - |
| dc.contributor.author | LAM, YYS | - |
| dc.contributor.author | Low, KH | - |
| dc.contributor.author | Chiu, P | - |
| dc.date.accessioned | 2017-08-25T02:48:35Z | - |
| dc.date.available | 2017-08-25T02:48:35Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.citation | Angewandte Chemie (International Edition), 2017, v. 56, p. 8879-8882 | - |
| dc.identifier.issn | 1433-7851 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/243004 | - |
| dc.description.abstract | An intramolecular (4+3) cycloaddition of epoxy and aziridinyl enolsilanes with benzene, naphthalene, and anthracene derivatives is reported. Highly functionalized polycyclic alcohols and amines are generated under relatively mild reaction conditions with yields up to 89 %. Optically enriched cycloadducts are obtained from cycloadditions of enantiomerically pure epoxides and aziridines. | - |
| dc.language | eng | - |
| dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home | - |
| dc.relation.ispartof | Angewandte Chemie (International Edition) | - |
| dc.rights | postprint: This is the accepted version of the following article: FULL CITE, which has been published in final form at [Link to final article]. Preprint This is the pre-peer reviewed version of the following article: FULL CITE, which has been published in final form at [Link to final article]. | - |
| dc.subject | arenes | - |
| dc.subject | cycloaddition | - |
| dc.subject | dearomatization | - |
| dc.subject | heterocycles | - |
| dc.subject | synthetic methods | - |
| dc.title | Dearomative Intramolecular (4+3) Cycloadditions of Arenes with Epoxy and Aziridinyl Enolsilanes | - |
| dc.type | Article | - |
| dc.identifier.email | Low, KH: khlow@hku.hk | - |
| dc.identifier.email | Chiu, P: pchiu@hku.hk | - |
| dc.identifier.authority | Chiu, P=rp00680 | - |
| dc.identifier.doi | 10.1002/anie.201704155 | - |
| dc.identifier.scopus | eid_2-s2.0-85021013396 | - |
| dc.identifier.hkuros | 274426 | - |
| dc.identifier.volume | 56 | - |
| dc.identifier.spage | 8879 | - |
| dc.identifier.epage | 8882 | - |
| dc.identifier.isi | WOS:000405308500051 | - |
| dc.publisher.place | Germany | - |
| dc.identifier.issnl | 1433-7851 | - |