From ynamides to highly substituted benzo[b]furans: gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates

A series of arylynamides with alkyloxy groups at the ortho position of the aryl group was prepared through a short alkylation/cross-coupling/amidation sequence. The gold-catalyzed conversion of these substrates combined both CO and CC formation steps, thus providing benzofurans with amine function...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Blanco Jaimes, Maria Camila (VerfasserIn) , Claus, Vanessa (VerfasserIn) , Rominger, Frank (VerfasserIn) , Hashmi, A. Stephen K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 6, 2013
In: Chemistry - a European journal
Year: 2013, Jahrgang: 19, Heft: 37, Pages: 12504-12511
ISSN:1521-3765
DOI:https://doi.org/10.1002/chem.201301595
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1002/chem.201301595
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201301595
Volltext
Verfasserangaben:Maria Camila Blanco Jaimes, Vanessa Weingand, Frank Rominger, and A. Stephen K. Hashmi

MARC

LEADER 00000caa a2200000 c 4500
001 1756666261
003 DE-627
005 20230426092552.0
007 cr uuu---uuuuu
008 210430s2013 xx |||||o 00| ||eng c
024 7 |a 10.1002/chem.201301595  |2 doi 
035 |a (DE-627)1756666261 
035 |a (DE-599)KXP1756666261 
035 |a (OCoLC)1341407537 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 30  |2 sdnb 
100 1 |a Blanco Jaimes, Maria Camila  |d 1985-  |e VerfasserIn  |0 (DE-588)1058987224  |0 (DE-627)797899332  |0 (DE-576)415058937  |4 aut 
245 1 0 |a From ynamides to highly substituted benzo[b]furans  |b gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates  |c Maria Camila Blanco Jaimes, Vanessa Weingand, Frank Rominger, and A. Stephen K. Hashmi 
264 1 |c August 6, 2013 
300 |a 8 
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 30.04.2021 
520 |a A series of arylynamides with alkyloxy groups at the ortho position of the aryl group was prepared through a short alkylation/cross-coupling/amidation sequence. The gold-catalyzed conversion of these substrates combined both CO and CC formation steps, thus providing benzofurans with amine functionalities at the 2-position and alkyl groups at the 3-position. Cross-over experiments showed that the alkyl-migration step was an intermolecular process. X-ray crystal-structure analysis of two of the products supported our structural assignment. In some cases, the corresponding benzofurans without the alkyl group at the 3-position were obtained as side-products, which were formed through a competing protodeauration process. 
650 4 |a cyclization 
650 4 |a gold 
650 4 |a heterocycles 
650 4 |a rearrangement 
650 4 |a ynamides 
700 1 |a Claus, Vanessa  |e VerfasserIn  |0 (DE-588)1059460238  |0 (DE-627)798480432  |0 (DE-576)415610966  |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 
700 1 |a Hashmi, A. Stephen K.  |d 1963-  |e VerfasserIn  |0 (DE-588)101199576X  |0 (DE-627)704823926  |0 (DE-576)169176665  |4 aut 
773 0 8 |i Enthalten in  |t Chemistry - a European journal  |d Weinheim : Wiley-VCH, 1995  |g 19(2013), 37, Seite 12504-12511  |h Online-Ressource  |w (DE-627)270935193  |w (DE-600)1478547-X  |w (DE-576)078707404  |x 1521-3765  |7 nnas  |a From ynamides to highly substituted benzo[b]furans gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates 
773 1 8 |g volume:19  |g year:2013  |g number:37  |g pages:12504-12511  |g extent:8  |a From ynamides to highly substituted benzo[b]furans gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates 
776 0 8 |i Erscheint auch als  |n Druck-Ausgabe  |t From ynamides to highly substituted benzo[b]​furans  |d 2013  |w (DE-627)1640875972  |w (DE-576)416010016 
856 4 0 |u https://doi.org/https://doi.org/10.1002/chem.201301595  |x Verlag  |x Resolving-System  |z lizenzpflichtig  |3 Volltext 
856 4 0 |u https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201301595  |x Verlag  |z lizenzpflichtig  |3 Volltext 
951 |a AR 
992 |a 20210430 
993 |a Article 
994 |a 2013 
998 |g 101199576X  |a Hashmi, A. Stephen K.  |m 101199576X:Hashmi, A. Stephen K.  |d 120000  |d 120100  |e 120000PH101199576X  |e 120100PH101199576X  |k 0/120000/  |k 1/120000/120100/  |p 4  |y j 
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 
998 |g 1059460238  |a Claus, Vanessa  |m 1059460238:Claus, Vanessa  |p 2 
998 |g 1058987224  |a Blanco Jaimes, Maria Camila  |m 1058987224:Blanco Jaimes, Maria Camila  |d 120000  |e 120000PB1058987224  |k 0/120000/  |p 1  |x j 
999 |a KXP-PPN1756666261  |e 3920282337 
BIB |a Y 
SER |a journal 
JSO |a {"language":["eng"],"note":["Gesehen am 30.04.2021"],"title":[{"title":"From ynamides to highly substituted benzo[b]furans","title_sort":"From ynamides to highly substituted benzo[b]furans","subtitle":"gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediates"}],"origin":[{"dateIssuedDisp":"August 6, 2013","dateIssuedKey":"2013"}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"person":[{"given":"Maria Camila","role":"aut","family":"Blanco Jaimes","display":"Blanco Jaimes, Maria Camila"},{"role":"aut","given":"Vanessa","family":"Claus","display":"Claus, Vanessa"},{"role":"aut","given":"Frank","family":"Rominger","display":"Rominger, Frank"},{"display":"Hashmi, A. Stephen K.","family":"Hashmi","given":"A. Stephen K.","role":"aut"}],"relHost":[{"disp":"From ynamides to highly substituted benzo[b]furans gold(I)-catalyzed 5-endo-dig-cyclization/rearrangement of alkylic oxonium intermediatesChemistry - a European journal","language":["eng"],"part":{"year":"2013","pages":"12504-12511","text":"19(2013), 37, Seite 12504-12511","extent":"8","volume":"19","issue":"37"},"note":["Fortsetzung der Druck-Ausgabe","Gesehen am 27. Februar 2017"],"title":[{"title_sort":"Chemistry - a European journal","title":"Chemistry - a European journal"}],"origin":[{"dateIssuedDisp":"1995-","publisherPlace":"Weinheim","dateIssuedKey":"1995","publisher":"Wiley-VCH"}],"type":{"media":"Online-Ressource","bibl":"periodical"},"recId":"270935193","pubHistory":["1.1995 -"],"physDesc":[{"extent":"Online-Ressource"}],"id":{"zdb":["1478547-X"],"issn":["1521-3765"],"eki":["270935193"],"doi":["10.1002/(ISSN)1521-3765"]}}],"id":{"doi":["10.1002/chem.201301595"],"eki":["1756666261"]},"recId":"1756666261","name":{"displayForm":["Maria Camila Blanco Jaimes, Vanessa Weingand, Frank Rominger, and A. Stephen K. Hashmi"]},"physDesc":[{"extent":"8 S."}]} 
SRT |a BLANCOJAIMFROMYNAMID6201