| dc.contributor.author |
Pingaew R. |
|
| dc.contributor.author |
Prachayasittikul S. |
|
| dc.contributor.author |
Ruchirawat S. |
|
| dc.contributor.author |
Prachayasittikul V. |
|
| dc.date.accessioned |
2021-04-05T03:32:48Z |
|
| dc.date.available |
2021-04-05T03:32:48Z |
|
| dc.date.issued |
2013 |
|
| dc.identifier.issn |
10018417 |
|
| dc.identifier.other |
2-s2.0-84883739431 |
|
| dc.identifier.uri |
https://ir.swu.ac.th/jspui/handle/123456789/13990 |
|
| dc.identifier.uri |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84883739431&doi=10.1016%2fj.cclet.2013.06.019&partnerID=40&md5=232d167bb5e17de63b4966fa85cdd733 |
|
| dc.description.abstract |
An operationally simple and eco-friendly protocol has been developed for the synthesis of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines 3 using the modified Pictet-Spengler reaction of N-sulfonylphenylethylamines 1 and various aldehydes 2 in the presence of tungstophosphoric acid hydrate. © 2013 Zhi-Jin Fan. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. |
|
| dc.title |
Tungstophosphoric acid catalyzed synthesis of N-sulfonyl-1,2,3,4- tetrahydroisoquinoline analogs |
|
| dc.type |
Article |
|
| dc.rights.holder |
Scopus |
|
| dc.identifier.bibliograpycitation |
Chinese Chemical Letters. Vol 24, No.10 (2013), p.941-944 |
|
| dc.identifier.doi |
10.1016/j.cclet.2013.06.019 |
|