Palladium-catalyzed oxidative arylacetoxylation of alkenes : synthesis of indole and indoline derivatives
A method for the oxidative arylacetoxylation of alkenes has been developed to synthesize indole and indoline derivatives from readily accessible substrates. The cinnamyl tethered anilines with picolinamide as a directing group provided 3-substituted indoles via intramolecular oxidative arylacetoxylation, and the 2-methyl substituted cinnamyl anilines furnished indoline derivatives with 3-position quaternary stereocenters in good to excellent yields via sequential intramolecular oxidative arylacetoxylation, hydrolysis and oxidation steps.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2017 |
---|---|
Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:53 |
---|---|
Enthalten in: |
Chemical communications (Cambridge, England) - 53(2017), 81 vom: 18. Okt., Seite 11205-11208 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Karnakanti, Shuklachary [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Completed 02.03.2018 Date Revised 02.03.2018 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.1039/c7cc06448a |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM276265068 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM276265068 | ||
003 | DE-627 | ||
005 | 20231225011620.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2017 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1039/c7cc06448a |2 doi | |
028 | 5 | 2 | |a pubmed24n0920.xml |
035 | |a (DE-627)NLM276265068 | ||
035 | |a (NLM)28956559 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Karnakanti, Shuklachary |e verfasserin |4 aut | |
245 | 1 | 0 | |a Palladium-catalyzed oxidative arylacetoxylation of alkenes |b synthesis of indole and indoline derivatives |
264 | 1 | |c 2017 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 02.03.2018 | ||
500 | |a Date Revised 02.03.2018 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a A method for the oxidative arylacetoxylation of alkenes has been developed to synthesize indole and indoline derivatives from readily accessible substrates. The cinnamyl tethered anilines with picolinamide as a directing group provided 3-substituted indoles via intramolecular oxidative arylacetoxylation, and the 2-methyl substituted cinnamyl anilines furnished indoline derivatives with 3-position quaternary stereocenters in good to excellent yields via sequential intramolecular oxidative arylacetoxylation, hydrolysis and oxidation steps | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Zang, Zhong-Lin |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Sheng |e verfasserin |4 aut | |
700 | 1 | |a Shao, Pan-Lin |e verfasserin |4 aut | |
700 | 1 | |a Hu, Ping |e verfasserin |4 aut | |
700 | 1 | |a He, Yun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Chemical communications (Cambridge, England) |d 1998 |g 53(2017), 81 vom: 18. Okt., Seite 11205-11208 |w (DE-627)NLM095512322 |x 1364-548X |7 nnns |
773 | 1 | 8 | |g volume:53 |g year:2017 |g number:81 |g day:18 |g month:10 |g pages:11205-11208 |
856 | 4 | 0 | |u http://dx.doi.org/10.1039/c7cc06448a |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 53 |j 2017 |e 81 |b 18 |c 10 |h 11205-11208 |