Yu M, Huang J, Zhu H, Shi D, Yang W, Liu Y
RSC Adv. 2024; 14(39):28585-28595.
PMID: 39247504
PMC: 11378031.
DOI: 10.1039/d4ra05596a.
Assani N, Delfau L, Smits P, Redon S, Kabri Y, Tomas-Mendivil E
Chem Sci. 2024; .
PMID: 39176246
PMC: 11337093.
DOI: 10.1039/d4sc04011b.
Barik S, Ranganathappa S, Biju A
Nat Commun. 2024; 15(1):5755.
PMID: 38982037
PMC: 11233592.
DOI: 10.1038/s41467-024-49799-5.
Bacaicoa S, Stenkvist S, Sunden H
Org Lett. 2024; 26(15):3114-3118.
PMID: 38551486
PMC: 11040713.
DOI: 10.1021/acs.orglett.4c00731.
Lv X, Su F, Long H, Lu F, Zeng Y, Liao M
Nat Commun. 2024; 15(1):958.
PMID: 38302464
PMC: 10834540.
DOI: 10.1038/s41467-024-45218-x.
On the Redox Properties of the Dimers of Thiazol-2-ylidenes That Are Relevant for Radical Catalysis.
Delfau L, Assani N, Nichilo S, Pecaut J, Philouze C, Broggi J
ACS Org Inorg Au. 2023; 3(3):136-142.
PMID: 37303499
PMC: 10251502.
DOI: 10.1021/acsorginorgau.3c00008.
Synthesis of N-, O-, and S-heterocycles from aryl/alkyl alkynyl aldehydes.
Doraghi F, Mohaghegh F, Hosseinchi Qareaghaj O, Larijani B, Mahdavi M
RSC Adv. 2023; 13(20):13947-13970.
PMID: 37181524
PMC: 10167737.
DOI: 10.1039/d3ra01778h.
Aerobic Oxidative N-Heterocyclic Carbene-Catalyzed Formal [3+3] Cyclization for the Synthesis of Tetrasubstituted Benzene Derivatives.
Bacaicoa S, Goossens E, Sunden H
Org Lett. 2022; 24(49):9146-9150.
PMID: 36469618
PMC: 9764416.
DOI: 10.1021/acs.orglett.2c03879.
Oxidative N-Heterocyclic Carbene Catalysis.
De Risi C, Brandolese A, Di Carmine G, Ragno D, Massi A, Bortolini O
Chemistry. 2022; 29(4):e202202467.
PMID: 36205918
PMC: 10099058.
DOI: 10.1002/chem.202202467.
Radical transformations for allene synthesis.
Li Y, Bao H
Chem Sci. 2022; 13(29):8491-8506.
PMID: 35974759
PMC: 9337727.
DOI: 10.1039/d2sc02573f.
First example of organocatalysis by cathodic N-heterocyclic carbene generation and accumulation using a divided electrochemical flow cell.
Rocco D, Folgueiras-Amador A, Brown R, Feroci M
Beilstein J Org Chem. 2022; 18:979-990.
PMID: 35965857
PMC: 9359202.
DOI: 10.3762/bjoc.18.98.
Electroredox carbene organocatalysis with iodide as promoter.
Zhou P, Li W, Lan J, Zhu T
Nat Commun. 2022; 13(1):3827.
PMID: 35780238
PMC: 9250514.
DOI: 10.1038/s41467-022-31453-7.
A C-symmetric -heterocyclic carbene catalysed oxidative spiroannulation of isatin-derived enals: highly enantioselective synthesis of spirooxindole δ-lactones.
Lin J, Cheng X, Tian X, Xu G, Luo Y, Xu P
RSC Adv. 2022; 8(28):15444-15447.
PMID: 35539478
PMC: 9080099.
DOI: 10.1039/c8ra02009d.
Enantioselective functionalization at the C4 position of pyridinium salts through NHC catalysis.
Choi H, Mathi G, Hong S, Hong S
Nat Commun. 2022; 13(1):1776.
PMID: 35365667
PMC: 8975994.
DOI: 10.1038/s41467-022-29462-7.
Critical Assessment of the Reducing Ability of Breslow-type Derivatives and Implications for Carbene-Catalyzed Radical Reactions*.
Delfau L, Nichilo S, Molton F, Broggi J, Tomas-Mendivil E, Martin D
Angew Chem Int Ed Engl. 2021; 60(51):26783-26789.
PMID: 34651408
PMC: 9299025.
DOI: 10.1002/anie.202111988.
Desymmetrization of Cyclic 1,3-Diketones under -Heterocyclic Carbene Organocatalysis: Access to Organofluorines with Multiple Stereogenic Centers.
Wang G, Zhang M, Guan Y, Zhang Y, Hong X, Wei C
Research (Wash D C). 2021; 2021:9867915.
PMID: 34549186
PMC: 8422277.
DOI: 10.34133/2021/9867915.
N-Heterocyclic Carbene/Carboxylic Acid Co-Catalysis Enables Oxidative Esterification of Demanding Aldehydes/Enals, at Low Catalyst Loading.
Harnying W, Sudkaow P, Biswas A, Berkessel A
Angew Chem Int Ed Engl. 2021; 60(36):19631-19636.
PMID: 34010504
PMC: 8457137.
DOI: 10.1002/anie.202104712.
Direct α-Acylation of Alkenes via N-Heterocyclic Carbene, Sulfinate, and Photoredox Cooperative Triple Catalysis.
Liu K, Studer A
J Am Chem Soc. 2021; 143(13):4903-4909.
PMID: 33760603
PMC: 8033569.
DOI: 10.1021/jacs.1c01022.
Acyl Donor Intermediates in N-Heterocyclic Carbene Catalysis: Acyl Azolium or Azolium Enolate?.
Biswas A, Neudorfl J, Schlorer N, Berkessel A
Angew Chem Int Ed Engl. 2020; 60(9):4507-4511.
PMID: 33140529
PMC: 7986403.
DOI: 10.1002/anie.202010348.
Organocatalytic Name Reactions Enabled by NHCs.
Dzieszkowski K, Baranska I, Mroczynska K, Slotwinski M, Rafinski Z
Materials (Basel). 2020; 13(16).
PMID: 32823580
PMC: 7475904.
DOI: 10.3390/ma13163574.
