211 related articles for article (PubMed ID: 23869442)
1. Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine.
Cordier CJ; Lundgren RJ; Fu GC
J Am Chem Soc; 2013 Jul; 135(30):10946-9. PubMed ID: 23869442
[TBL] [Abstract][Full Text] [Related]
2. Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents.
Binder JT; Cordier CJ; Fu GC
J Am Chem Soc; 2012 Oct; 134(41):17003-6. PubMed ID: 23039358
[TBL] [Abstract][Full Text] [Related]
3. Enantioconvergent Cross-Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes.
Schwarzwalder GM; Matier CD; Fu GC
Angew Chem Int Ed Engl; 2019 Mar; 58(11):3571-3574. PubMed ID: 30650228
[TBL] [Abstract][Full Text] [Related]
4. Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF3 and an Alkyl Group.
Liang Y; Fu GC
J Am Chem Soc; 2015 Aug; 137(30):9523-6. PubMed ID: 26203662
[TBL] [Abstract][Full Text] [Related]
5. Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.
Zultanski SL; Fu GC
J Am Chem Soc; 2011 Oct; 133(39):15362-4. PubMed ID: 21913638
[TBL] [Abstract][Full Text] [Related]
6. Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent Negishi arylations and alkenylations of racemic α-bromonitriles.
Choi J; Fu GC
J Am Chem Soc; 2012 Jun; 134(22):9102-5. PubMed ID: 22612264
[TBL] [Abstract][Full Text] [Related]
7. Enantioconvergent Alkylations of Amines by Alkyl Electrophiles: Copper-Catalyzed Nucleophilic Substitutions of Racemic α-Halolactams by Indoles.
Bartoszewicz A; Matier CD; Fu GC
J Am Chem Soc; 2019 Sep; 141(37):14864-14869. PubMed ID: 31496239
[TBL] [Abstract][Full Text] [Related]
8. Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic Electrophiles.
Wang Z; Bachman S; Dudnik AS; Fu GC
Angew Chem Int Ed Engl; 2018 Oct; 57(44):14529-14532. PubMed ID: 30079625
[TBL] [Abstract][Full Text] [Related]
9. Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins.
Owston NA; Fu GC
J Am Chem Soc; 2010 Sep; 132(34):11908-9. PubMed ID: 20701271
[TBL] [Abstract][Full Text] [Related]
10. Chromium(II)-Catalyzed Diastereoselective and Chemoselective Csp
Li J; Ren Q; Cheng X; Karaghiosoff K; Knochel P
J Am Chem Soc; 2019 Nov; 141(45):18127-18135. PubMed ID: 31634428
[TBL] [Abstract][Full Text] [Related]
11. Nickel-catalyzed asymmetric negishi cross-couplings of secondary allylic chlorides with alkylzincs.
Son S; Fu GC
J Am Chem Soc; 2008 Mar; 130(9):2756-7. PubMed ID: 18257579
[TBL] [Abstract][Full Text] [Related]
12. Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents.
Smith SW; Fu GC
J Am Chem Soc; 2008 Sep; 130(38):12645-7. PubMed ID: 18763769
[TBL] [Abstract][Full Text] [Related]
13. Catalytic Enantioselective α-Alkylation of Amides by Unactivated Alkyl Electrophiles.
Tong X; Schneck F; Fu GC
J Am Chem Soc; 2022 Aug; 144(32):14856-14863. PubMed ID: 35925763
[TBL] [Abstract][Full Text] [Related]
14. Stereoselective Functionalization of Racemic Cyclopropylzinc Reagents via Enantiodivergent Relay Coupling.
An L; Tong FF; Zhang S; Zhang X
J Am Chem Soc; 2020 Jul; 142(27):11884-11892. PubMed ID: 32530615
[TBL] [Abstract][Full Text] [Related]
15. Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles.
Iwasaki T; Kambe N
Top Curr Chem (Cham); 2016 Oct; 374(5):66. PubMed ID: 27580894
[TBL] [Abstract][Full Text] [Related]
16. Enantioselective C(sp
Zhou J; Wang D; Xu W; Hu Z; Xu T
J Am Chem Soc; 2023 Feb; 145(4):2081-2087. PubMed ID: 36688920
[TBL] [Abstract][Full Text] [Related]
17. Enantioselective Csp3-Csp3 formation by nickel-catalyzed enantioconvergent cross-electrophile alkyl-alkyl coupling of unactivated alkyl halides.
Zhao WT; Shu W
Sci Adv; 2023 Jul; 9(27):eadg9898. PubMed ID: 37418514
[TBL] [Abstract][Full Text] [Related]
18. Control of Vicinal Stereocenters through Nickel-Catalyzed Alkyl-Alkyl Cross-Coupling.
Mu X; Shibata Y; Makida Y; Fu GC
Angew Chem Int Ed Engl; 2017 May; 56(21):5821-5824. PubMed ID: 28421708
[TBL] [Abstract][Full Text] [Related]
19. Quaternary stereocentres via catalytic enantioconvergent nucleophilic substitution reactions of tertiary alkyl halides.
Wang Z; Yang ZP; Fu GC
Nat Chem; 2021 Mar; 13(3):236-242. PubMed ID: 33432109
[TBL] [Abstract][Full Text] [Related]
20. Nickel/bis(oxazoline)-catalyzed asymmetric Negishi arylations of racemic secondary benzylic electrophiles to generate enantioenriched 1,1-diarylalkanes.
Do HQ; Chandrashekar ER; Fu GC
J Am Chem Soc; 2013 Nov; 135(44):16288-91. PubMed ID: 24164502
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
