These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
146 related articles for article (PubMed ID: 34669225)
1. Catalytic Asymmetric Halogenation/Semipinacol Rearrangement of 3-Hydroxyl-3-vinyl Oxindoles: A Stereodivergent Kinetic Resolution Process. Dai L; Liu W; Zhou Y; Zeng Z; Hu X; Cao W; Feng X Angew Chem Int Ed Engl; 2021 Dec; 60(51):26599-26603. PubMed ID: 34669225 [TBL] [Abstract][Full Text] [Related]
2. Asymmetric Catalytic Vinylogous Addition Reactions Initiated by Meinwald Rearrangement of Vinyl Epoxides. Xu J; Song Y; He J; Dong S; Lin L; Feng X Angew Chem Int Ed Engl; 2021 Jun; 60(26):14521-14527. PubMed ID: 33826200 [TBL] [Abstract][Full Text] [Related]
3. Stereoselective construction of quaternary carbon stereocenters via a semipinacol rearrangement strategy. Wang B; Tu YQ Acc Chem Res; 2011 Nov; 44(11):1207-22. PubMed ID: 21728380 [TBL] [Abstract][Full Text] [Related]
4. Copper-Catalyzed Enantioselective Domino Arylation/Semipinacol Rearrangement of Allylic Alcohols with Diaryliodonium Salts. Wu H; Wang Q; Zhu J Chemistry; 2017 Sep; 23(53):13037-13041. PubMed ID: 28758703 [TBL] [Abstract][Full Text] [Related]
5. Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles. Cao ZY; Zhou F; Zhou J Acc Chem Res; 2018 Jun; 51(6):1443-1454. PubMed ID: 29808678 [TBL] [Abstract][Full Text] [Related]
6. Enantioselective Ir-Catalyzed Allyl Alkylation/Semipinacol Rearrangement. Zhao S; Yue W; Yang M; Li X; Chen B; Gao Y; Yu W; Ni HL; Hu P; Wang BQ; Cao P Org Lett; 2024 Feb; 26(6):1224-1228. PubMed ID: 38305744 [TBL] [Abstract][Full Text] [Related]
7. Organocatalytic asymmetric fluorination/semipinacol rearrangement: an efficient approach to chiral β-fluoroketones. Chen ZM; Yang BM; Chen ZH; Zhang QW; Wang M; Tu YQ Chemistry; 2012 Oct; 18(41):12950-4. PubMed ID: 22936470 [TBL] [Abstract][Full Text] [Related]
8. Lewis Base/Brønsted Acid Co-catalyzed Enantioselective Sulfenylation/Semipinacol Rearrangement of Di- and Trisubstituted Allylic Alcohols. Xie YY; Chen ZM; Luo HY; Shao H; Tu YQ; Bao X; Cao RF; Zhang SY; Tian JM Angew Chem Int Ed Engl; 2019 Sep; 58(36):12491-12496. PubMed ID: 31293063 [TBL] [Abstract][Full Text] [Related]
9. Nickel(II)-Catalyzed Asymmetric Propargyl [2,3] Wittig Rearrangement of Oxindole Derivatives: A Chiral Amplification Effect. Xu X; Zhang J; Dong S; Lin L; Lin X; Liu X; Feng X Angew Chem Int Ed Engl; 2018 Jul; 57(28):8734-8738. PubMed ID: 29782078 [TBL] [Abstract][Full Text] [Related]
10. Lewis base mediated halogenation/semipinacol rearrangement of diazo compounds: new access to α-halo-quaternary ketones. Mao H; Tang Z; Hu H; Cheng Y; Zheng WH; Zhu C Chem Commun (Camb); 2014 Sep; 50(68):9773-5. PubMed ID: 25019673 [TBL] [Abstract][Full Text] [Related]
11. Oxyallyl cation promoted dearomative semipinacol rearrangement: a facile stereodivergent synthesis of spiro-indolines with contiguous quaternary centers. Xie YY; Wang YP; Zhao XJ; Wang AF; Chen ZM; Tu YQ Chem Commun (Camb); 2021 Jul; 57(54):6632-6635. PubMed ID: 34124740 [TBL] [Abstract][Full Text] [Related]
12. Stereodivergent synthesis of vicinal quaternary-quaternary stereocenters and bioactive hyperolactones. Zheng H; Wang Y; Xu C; Xu X; Lin L; Liu X; Feng X Nat Commun; 2018 May; 9(1):1968. PubMed ID: 29773786 [TBL] [Abstract][Full Text] [Related]
13. Asymmetric Catalytic Formal 1,4-Allylation of β,γ-Unsaturated α-Ketoesters: Allylboration/Oxy-Cope Rearrangement. Tang Q; Fu K; Ruan P; Dong S; Su Z; Liu X; Feng X Angew Chem Int Ed Engl; 2019 Aug; 58(34):11846-11851. PubMed ID: 31237402 [TBL] [Abstract][Full Text] [Related]
14. Organocatalytic asymmetric halogenation/semipinacol rearrangement: highly efficient synthesis of chiral α-oxa-quaternary β-haloketones. Chen ZM; Zhang QW; Chen ZH; Li H; Tu YQ; Zhang FM; Tian JM J Am Chem Soc; 2011 Jun; 133(23):8818-21. PubMed ID: 21548637 [TBL] [Abstract][Full Text] [Related]
15. A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: highly efficient synthesis of functionalized 2-quinolone derivatives. Li W; Liu X; Hao X; Cai Y; Lin L; Feng X Angew Chem Int Ed Engl; 2012 Aug; 51(34):8644-7. PubMed ID: 22821752 [TBL] [Abstract][Full Text] [Related]
16. Catalytic Enantioselective and Diastereoselective Allylic Alkylation with Fluoroenolates: Efficient Access to C3-Fluorinated and All-Carbon Quaternary Oxindoles. Balaraman K; Wolf C Angew Chem Int Ed Engl; 2017 Jan; 56(5):1390-1395. PubMed ID: 28026079 [TBL] [Abstract][Full Text] [Related]
17. Catalytic asymmetric synthesis of spirocyclobutyl oxindoles and beyond Zhong X; Tan J; Qiao J; Zhou Y; Lv C; Su Z; Dong S; Feng X Chem Sci; 2021 Jul; 12(29):9991-9997. PubMed ID: 34377393 [TBL] [Abstract][Full Text] [Related]
18. Highly enantioselective synthesis of 3-amino-2-oxindole derivatives: catalytic asymmetric alpha-amination of 3-substituted 2-oxindoles with a chiral scandium complex. Yang Z; Wang Z; Bai S; Shen K; Chen D; Liu X; Lin L; Feng X Chemistry; 2010 Jun; 16(22):6632-7. PubMed ID: 20408167 [TBL] [Abstract][Full Text] [Related]
19. Asymmetric 1,2-reduction of enones with potassium borohydride catalyzed by chiral N,N'-dioxide-scandium(III) complexes. He P; Liu X; Zheng H; Li W; Lin L; Feng X Org Lett; 2012 Oct; 14(19):5134-7. PubMed ID: 23013322 [TBL] [Abstract][Full Text] [Related]
20. Chiral N,N'-dioxides: new ligands and organocatalysts for catalytic asymmetric reactions. Liu X; Lin L; Feng X Acc Chem Res; 2011 Aug; 44(8):574-87. PubMed ID: 21702458 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]