Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines
© 2016 Elsevier Ltd A convenient one-pot protocol for the synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines is reported. In the presence of the Ph 3 P–I 2 /Et 3 N system, a variety of secondary amides were smoothly reacted with primary or secondary amines to afford the corresponding...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Journal |
| Published: |
2017
|
| Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994028119&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42258 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Chiang Mai University |
| id |
th-cmuir.6653943832-42258 |
|---|---|
| record_format |
dspace |
| spelling |
th-cmuir.6653943832-422582017-09-28T04:26:05Z Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines Phakhodee W. Wangngae S. Wiriya N. Pattarawarapan M. © 2016 Elsevier Ltd A convenient one-pot protocol for the synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines is reported. In the presence of the Ph 3 P–I 2 /Et 3 N system, a variety of secondary amides were smoothly reacted with primary or secondary amines to afford the corresponding amidines in good to excellent yields under mild conditions. 2017-09-28T04:26:05Z 2017-09-28T04:26:05Z 2016-01-01 Journal 00404039 2-s2.0-84994028119 10.1016/j.tetlet.2016.10.069 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994028119&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42258 |
| institution |
Chiang Mai University |
| building |
Chiang Mai University Library |
| country |
Thailand |
| collection |
CMU Intellectual Repository |
| description |
© 2016 Elsevier Ltd A convenient one-pot protocol for the synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines is reported. In the presence of the Ph 3 P–I 2 /Et 3 N system, a variety of secondary amides were smoothly reacted with primary or secondary amines to afford the corresponding amidines in good to excellent yields under mild conditions. |
| format |
Journal |
| author |
Phakhodee W. Wangngae S. Wiriya N. Pattarawarapan M. |
| spellingShingle |
Phakhodee W. Wangngae S. Wiriya N. Pattarawarapan M. Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| author_facet |
Phakhodee W. Wangngae S. Wiriya N. Pattarawarapan M. |
| author_sort |
Phakhodee W. |
| title |
Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| title_short |
Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| title_full |
Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| title_fullStr |
Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| title_full_unstemmed |
Ph<inf>3</inf>P/I<inf>2</inf>-mediated synthesis of N,N′-disubstituted and N,N,N′-trisubstituted amidines |
| title_sort |
ph<inf>3</inf>p/i<inf>2</inf>-mediated synthesis of n,n′-disubstituted and n,n,n′-trisubstituted amidines |
| publishDate |
2017 |
| url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994028119&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42258 |
| _version_ |
1681422155083939840 |