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1.
Insights into Recent Nickel-Catalyzed Reductive and Redox C-C Coupling of Electrophiles, C(sp3)-H Bonds and Alkenes.
Acc Chem Res
; 57(8): 1149-1162, 2024 Apr 16.
Article
in English
| MEDLINE | ID: mdl-38547518
2.
Expeditious preparation of ß-sec-alkyl vicinal amino alcohols used for chiral ligand synthesis.
Org Biomol Chem
; 21(30): 6111-6114, 2023 Aug 02.
Article
in English
| MEDLINE | ID: mdl-37462436
3.
Retraction: Deoxygenative cross-electrophile coupling of benzyl chloroformates with aryl iodides.
Org Biomol Chem
; 21(31): 6424, 2023 Aug 09.
Article
in English
| MEDLINE | ID: mdl-37493463
4.
Nickel-catalyzed formation of quaternary carbon centers using tertiary alkyl electrophiles.
Chem Soc Rev
; 50(6): 4162-4184, 2021 Mar 21.
Article
in English
| MEDLINE | ID: mdl-33533345
5.
Nickel-Catalyzed Thermal Redox Functionalization of C(sp3 )-H Bonds with Carbon Electrophiles.
Angew Chem Int Ed Engl
; 61(22): e202201662, 2022 05 23.
Article
in English
| MEDLINE | ID: mdl-35293093
6.
Cross-Electrophile Couplings of Activated and Sterically Hindered Halides and Alcohol Derivatives.
Acc Chem Res
; 53(9): 1833-1845, 2020 09 15.
Article
in English
| MEDLINE | ID: mdl-32840998
7.
Nickel-catalyzed reductive 1,3-diene formation from the cross-coupling of vinyl bromides.
Org Biomol Chem
; 19(22): 4887-4890, 2021 06 09.
Article
in English
| MEDLINE | ID: mdl-34021299
8.
Nickel-Catalyzed, Regio- and Enantioselective Benzylic Alkenylation of Olefins with Alkenyl Bromide.
Angew Chem Int Ed Engl
; 60(8): 4060-4064, 2021 Feb 19.
Article
in English
| MEDLINE | ID: mdl-33171012
9.
Diverse Synthesis of Chiral Trifluoromethylated Alkanes via Nickel-Catalyzed Asymmetric Reductive Cross-Coupling Fluoroalkylation.
Angew Chem Int Ed Engl
; 60(18): 9947-9952, 2021 04 26.
Article
in English
| MEDLINE | ID: mdl-33569847
10.
Zn-Mediated Fragmentation of Tertiary Alkyl Oxalates Enabling Formation of Alkylated and Arylated Quaternary Carbon Centers.
J Am Chem Soc
; 141(2): 820-824, 2019 01 16.
Article
in English
| MEDLINE | ID: mdl-30571912
11.
AAAA-DDDD Quadruple H-Bond-Assisted Ionic Interactions: Robust Bis(guanidinium)/Dicarboxylate Heteroduplexes in Water.
J Am Chem Soc
; 141(51): 20146-20154, 2019 12 26.
Article
in English
| MEDLINE | ID: mdl-31789022
12.
Divergent Total Syntheses of C3 a-C7' Linked Diketopiperazine Alkaloids (+)-Asperazine and (+)-Pestalazineâ A Enabled by a Ni-Catalyzed Reductive Coupling of Tertiary Alkyl Chloride.
Chemistry
; 25(4): 989-992, 2019 Jan 18.
Article
in English
| MEDLINE | ID: mdl-30447110
13.
Deoxygenative cross-electrophile coupling of benzyl chloroformates with aryl iodides.
Org Biomol Chem
; 17(17): 4230-4233, 2019 04 24.
Article
in English
| MEDLINE | ID: mdl-30951058
14.
Ni-Catalyzed Reductive Coupling of Electron-Rich Aryl Iodides with Tertiary Alkyl Halides.
J Am Chem Soc
; 140(43): 14490-14497, 2018 10 31.
Article
in English
| MEDLINE | ID: mdl-30296073
15.
Nickel-Catalyzed Reductive Allylation of Tertiary Alkyl Halides with Allylic Carbonates.
Angew Chem Int Ed Engl
; 56(42): 13103-13106, 2017 10 09.
Article
in English
| MEDLINE | ID: mdl-28834053
16.
Ni-catalyzed reductive coupling of α-halocarbonyl derivatives with vinyl bromides.
Org Biomol Chem
; 14(48): 11332-11335, 2016 Dec 28.
Article
in English
| MEDLINE | ID: mdl-27878154
17.
Preparation of Vinyl Arenes by Nickel-Catalyzed Reductive Coupling of Aryl Halides with Vinyl Bromides.
Angew Chem Int Ed Engl
; 55(50): 15544-15548, 2016 12 12.
Article
in English
| MEDLINE | ID: mdl-27862759
18.
Corrigendum: Diverse Synthesis of Chiral Trifluoromethylated Alkanes via Nickel-Catalyzed Asymmetric Reductive Cross-Coupling Fluoroalkylation.
Angew Chem Int Ed Engl
; 60(27): 14735, 2021 Jun 25.
Article
in English
| MEDLINE | ID: mdl-34145707
19.
Nickel-Catalyzed Reductive Coupling of Aryl Bromides with Tertiary Alkyl Halides.
J Am Chem Soc
; 137(36): 11562-5, 2015 Sep 16.
Article
in English
| MEDLINE | ID: mdl-26325479
20.
Ni-catalyzed reductive addition of alkyl halides to isocyanides.
Org Biomol Chem
; 13(47): 11418-21, 2015 Dec 21.
Article
in English
| MEDLINE | ID: mdl-26524544