Photoredox and NHC Enabled Deoxygenative Alcohol Homologation via Formal 1,2-Addition
A highly efficient photoinduced iron-catalyzed method has been developed for the direct use of alcohols as surrogates for organometallic reagents in the synthesis of tertiary alcohols. This method can be applied to both primary and secondary alcohols with diverse structures, enabling their reaction with aryl ketones under mild conditions. A variety of functional groups, including those that are typically reactive under conventional tertiary alcohol synthesis conditions, are compatible. Mechanistically, this reaction proceeds through the direct addition of the radical to the carbonyl pathway.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:26 |
---|---|
Enthalten in: |
Organic letters - 26(2024), 1 vom: 12. Jan., Seite 264-268 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Song, Shuo [VerfasserIn] |
---|
Links: |
---|
Themen: |
---|
Anmerkungen: |
Date Revised 12.01.2024 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.1021/acs.orglett.3c03857 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM366383183 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM366383183 | ||
003 | DE-627 | ||
005 | 20240114234347.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231229s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/acs.orglett.3c03857 |2 doi | |
028 | 5 | 2 | |a pubmed24n1257.xml |
035 | |a (DE-627)NLM366383183 | ||
035 | |a (NLM)38147643 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Song, Shuo |e verfasserin |4 aut | |
245 | 1 | 0 | |a Photoredox and NHC Enabled Deoxygenative Alcohol Homologation via Formal 1,2-Addition |
264 | 1 | |c 2024 | |
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 Revised 12.01.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a A highly efficient photoinduced iron-catalyzed method has been developed for the direct use of alcohols as surrogates for organometallic reagents in the synthesis of tertiary alcohols. This method can be applied to both primary and secondary alcohols with diverse structures, enabling their reaction with aryl ketones under mild conditions. A variety of functional groups, including those that are typically reactive under conventional tertiary alcohol synthesis conditions, are compatible. Mechanistically, this reaction proceeds through the direct addition of the radical to the carbonyl pathway | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Li, Zhongxian |e verfasserin |4 aut | |
700 | 1 | |a Wang, Lele |e verfasserin |4 aut | |
700 | 1 | |a Zeng, Tianlong |e verfasserin |4 aut | |
700 | 1 | |a Hu, Qiang |e verfasserin |4 aut | |
700 | 1 | |a Zhu, Jun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Organic letters |d 1999 |g 26(2024), 1 vom: 12. Jan., Seite 264-268 |w (DE-627)NLM106817639 |x 1523-7052 |7 nnns |
773 | 1 | 8 | |g volume:26 |g year:2024 |g number:1 |g day:12 |g month:01 |g pages:264-268 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/acs.orglett.3c03857 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 26 |j 2024 |e 1 |b 12 |c 01 |h 264-268 |