| dc.contributor.author | Mahajan, Suruchi | |
| dc.contributor.author | Chauhan, Pankaj | |
| dc.contributor.author | Kaya, Uğur | |
| dc.contributor.author | Deckers, Kristina | |
| dc.contributor.author | Rissanen, Kari | |
| dc.contributor.author | Enders, Dieter | |
| dc.date.accessioned | 2017-07-03T10:04:31Z | |
| dc.date.available | 2018-05-31T21:35:43Z | |
| dc.date.issued | 2017 | |
| dc.identifier.citation | Mahajan, S., Chauhan, P., Kaya, U., Deckers, K., Rissanen, K., & Enders, D. (2017). Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction. <i>Chemical Communications</i>, <i>53</i>(49), 6633-6636. <a href="https://doi.org/10.1039/C7CC02874A" target="_blank">https://doi.org/10.1039/C7CC02874A</a> | |
| dc.identifier.other | CONVID_27044350 | |
| dc.identifier.other | TUTKAID_74012 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/54809 | |
| dc.description.abstract | A new organocatalytic enantioselective Strecker reaction of
pyrazolone-derived ketimine electrophiles has been developed.
Using pseudo-enantiomeric squaramide catalysts the nucleophilic
1,2-addition of trimethylsilyl cyanide to the ketimines efficiently
provides a direct entry to both enantiomers of pyrazolone α-
aminonitrile derivatives at will in good yields and high
enantioselectivities for a wide variety of substrates. | |
| dc.language.iso | eng | |
| dc.publisher | Royal Society of Chemistry | |
| dc.relation.ispartofseries | Chemical Communications | |
| dc.subject.other | enantioselective synthesis | |
| dc.subject.other | Strecker reaction | |
| dc.title | Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201706283130 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Nanoscience Center | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.contributor.oppiaine | Nanoscience Center | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2017-06-28T03:17:41Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 6633-6636 | |
| dc.relation.issn | 1359-7345 | |
| dc.relation.numberinseries | 49 | |
| dc.relation.volume | 53 | |
| dc.type.version | acceptedVersion | |
| dc.rights.copyright | © The Royal Society of Chemistry 2017. This is a final draft version of an article whose final and definitive form has been published by RSC. Published in this repository with the kind permission of the publisher. | |
| dc.rights.accesslevel | openAccess | fi |
| dc.relation.doi | 10.1039/C7CC02874A | |
| dc.type.okm | A1 | |
