Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid
The use of trans-4-isopropylcyclohexanecarboxylic acid as a substitution for the carboxylic acid component in the Ugi multicomponent condensation that leads to (1R,4R)-N-(2-(cyclohexylamino)-2-oxo-4-isopropylcyclohexane-1-carboxamide derivatives is described for the first time. One pot, clean reacti...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
01 February 2018
|
| In: |
Monatshefte für Chemie
Year: 2018, Volume: 149, Issue: 3, Pages: 625-633 |
| ISSN: | 1434-4475 |
| DOI: | 10.1007/s00706-017-2086-6 |
| Online Access: | Verlag, Volltext: https://doi.org/10.1007/s00706-017-2086-6
|
| Author Notes: | Sorour Ramezanpour, Akram Panahi, Frank Rominger |
MARC
| LEADER | 00000caa a2200000 c 4500 | ||
|---|---|---|---|
| 001 | 1663265593 | ||
| 003 | DE-627 | ||
| 005 | 20220816134555.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 190415s2018 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1007/s00706-017-2086-6 |2 doi | |
| 035 | |a (DE-627)1663265593 | ||
| 035 | |a (DE-599)KXP1663265593 | ||
| 035 | |a (OCoLC)1341209664 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rda | ||
| 041 | |a eng | ||
| 084 | |a 30 |2 sdnb | ||
| 100 | 1 | |a Ramezanpour, Sorour |e VerfasserIn |0 (DE-588)116010770X |0 (DE-627)1023260301 |0 (DE-576)505521989 |4 aut | |
| 245 | 1 | 0 | |a Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid |c Sorour Ramezanpour, Akram Panahi, Frank Rominger |
| 264 | 1 | |c 01 February 2018 | |
| 300 | |a 9 | ||
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Gesehen am 15.04.2019 | ||
| 520 | |a The use of trans-4-isopropylcyclohexanecarboxylic acid as a substitution for the carboxylic acid component in the Ugi multicomponent condensation that leads to (1R,4R)-N-(2-(cyclohexylamino)-2-oxo-4-isopropylcyclohexane-1-carboxamide derivatives is described for the first time. One pot, clean reaction, and excellent yields are some advantages of this protocol.Graphical abstract Open image in new window | ||
| 650 | 4 | |a Amino acid-derived | |
| 650 | 4 | |a Multicomponent condensation | |
| 650 | 4 | |a Trans-4-isopropylcyclohexanecarboxylic acid | |
| 700 | 1 | |a Panahi, Akram |e VerfasserIn |4 aut | |
| 700 | 1 | |a Rominger, Frank |d 1964- |e VerfasserIn |0 (DE-588)1019978228 |0 (DE-627)691067821 |0 (DE-576)359202756 |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Monatshefte für Chemie |d Wien [u.a.] : Springer, 1880 |g 149(2018), 3, Seite 625-633 |h Online-Ressource |w (DE-627)25462992X |w (DE-600)1462037-6 |w (DE-576)074529331 |x 1434-4475 |7 nnas |a Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid |
| 773 | 1 | 8 | |g volume:149 |g year:2018 |g number:3 |g pages:625-633 |g extent:9 |a Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid |
| 856 | 4 | 0 | |u https://doi.org/10.1007/s00706-017-2086-6 |x Verlag |x Resolving-System |3 Volltext |
| 951 | |a AR | ||
| 992 | |a 20190415 | ||
| 993 | |a Article | ||
| 994 | |a 2018 | ||
| 998 | |g 1019978228 |a Rominger, Frank |m 1019978228:Rominger, Frank |d 120000 |d 120100 |e 120000PR1019978228 |e 120100PR1019978228 |k 0/120000/ |k 1/120000/120100/ |p 3 |y j | ||
| 999 | |a KXP-PPN1663265593 |e 3422471626 | ||
| BIB | |a Y | ||
| SER | |a journal | ||
| JSO | |a {"relHost":[{"type":{"media":"Online-Ressource","bibl":"periodical"},"pubHistory":["1.1880 -"],"recId":"25462992X","disp":"Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acidMonatshefte für Chemie","language":["eng"],"titleAlt":[{"title":"Monatshefte für Chemie und verwandte Teile anderer Wissenschaften"}],"physDesc":[{"extent":"Online-Ressource"}],"part":{"year":"2018","pages":"625-633","text":"149(2018), 3, Seite 625-633","volume":"149","extent":"9","issue":"3"},"id":{"issn":["1434-4475"],"zdb":["1462037-6"],"eki":["25462992X"]},"note":["Gesehen am 31.10.05"],"titleTranslated":[{"translated":"Chemical monthly"}],"origin":[{"publisher":"Springer","dateIssuedDisp":"1880-","dateIssuedKey":"1880","publisherPlace":"Wien [u.a.]"}],"title":[{"title":"Monatshefte für Chemie","subtitle":"an international journal of chemistry = Chemical monthly","title_sort":"Monatshefte für Chemie"}]}],"note":["Gesehen am 15.04.2019"],"physDesc":[{"extent":"9 S."}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"id":{"doi":["10.1007/s00706-017-2086-6"],"eki":["1663265593"]},"language":["eng"],"title":[{"title":"Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid","title_sort":"Diastereoselective synthesis of peptidomimetics in one-pot Ugi reaction using trans-4-isopropylcyclohexanecarboxylic acid"}],"person":[{"display":"Ramezanpour, Sorour","given":"Sorour","family":"Ramezanpour","role":"aut"},{"family":"Panahi","display":"Panahi, Akram","given":"Akram","role":"aut"},{"given":"Frank","display":"Rominger, Frank","family":"Rominger","role":"aut"}],"recId":"1663265593","origin":[{"dateIssuedKey":"2018","dateIssuedDisp":"01 February 2018"}],"name":{"displayForm":["Sorour Ramezanpour, Akram Panahi, Frank Rominger"]}} | ||
| SRT | |a RAMEZANPOUDIASTEREOS0120 | ||