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Items: 1 to 20 of 113

1.

Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update.

Li C, Ragab SS, Liu G, Tang W.

Nat Prod Rep. 2019 Sep 13. doi: 10.1039/c9np00039a. [Epub ahead of print] Review.

PMID:
31515549
2.

Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles.

Cao ZY, Zhou F, Zhou J.

Acc Chem Res. 2018 Jun 19;51(6):1443-1454. doi: 10.1021/acs.accounts.8b00097. Epub 2018 May 29.

PMID:
29808678
3.

Catalytic enantioselective construction of quaternary stereocenters: assembly of key building blocks for the synthesis of biologically active molecules.

Liu Y, Han SJ, Liu WB, Stoltz BM.

Acc Chem Res. 2015 Mar 17;48(3):740-51. doi: 10.1021/ar5004658. Epub 2015 Feb 25.

5.

The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters.

Corey EJ, Guzman-Perez A.

Angew Chem Int Ed Engl. 1998 Mar 2;37(4):388-401. doi: 10.1002/(SICI)1521-3773(19980302)37:4<388::AID-ANIE388>3.0.CO;2-V. Review.

PMID:
29711174
6.

P-Chiral Phosphorus Ligands Based on a 2,3-Dihydrobenzo[ d][1,3]oxaphosphole Motif for Asymmetric Catalysis.

Xu G, Senanayake CH, Tang W.

Acc Chem Res. 2019 Apr 16;52(4):1101-1112. doi: 10.1021/acs.accounts.9b00029. Epub 2019 Mar 8.

PMID:
30848882
7.

Efficient syntheses of (-)-crinine and (-)-aspidospermidine, and the formal synthesis of (-)-minfiensine by enantioselective intramolecular dearomative cyclization.

Du K, Yang H, Guo P, Feng L, Xu G, Zhou Q, Chung LW, Tang W.

Chem Sci. 2017 Sep 1;8(9):6247-6256. doi: 10.1039/c7sc01859b. Epub 2017 Jul 3.

8.

Catalytic enantioselective Nazarov cyclization: construction of vicinal all-carbon-atom quaternary stereocenters.

Jolit A, Walleser PM, Yap GP, Tius MA.

Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6180-3. doi: 10.1002/anie.201403587. Epub 2014 May 18.

PMID:
24838340
9.

Construction of Acyclic Quaternary Carbon Stereocenters by Catalytic Asymmetric Hydroalkynylation of Unactivated Alkenes.

Wang ZX, Li BJ.

J Am Chem Soc. 2019 Jun 12;141(23):9312-9320. doi: 10.1021/jacs.9b03027. Epub 2019 Jun 4.

PMID:
31117476
10.

Construction of Axially Chiral Compounds via Asymmetric Organocatalysis.

Wang YB, Tan B.

Acc Chem Res. 2018 Feb 20;51(2):534-547. doi: 10.1021/acs.accounts.7b00602. Epub 2018 Feb 8.

PMID:
29419282
11.

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 17;9(1):1968. doi: 10.1038/s41467-018-04123-w.

12.

Stereoselective construction of quaternary carbon stereocenters via a semipinacol rearrangement strategy.

Wang B, Tu YQ.

Acc Chem Res. 2011 Nov 15;44(11):1207-22. doi: 10.1021/ar200082p. Epub 2011 Jul 6.

PMID:
21728380
13.

Enantioselective Construction of Quaternary Stereocenters.

Christoffers J, Mann A.

Angew Chem Int Ed Engl. 2001 Dec 17;40(24):4591-4597.

PMID:
12404360
14.

Enantioselective formation of cyano-bearing all-carbon quaternary stereocenters: desymmetrization by copper-catalyzed N-arylation.

Zhou F, Cheng GJ, Yang W, Long Y, Zhang S, Wu YD, Zhang X, Cai Q.

Angew Chem Int Ed Engl. 2014 Sep 1;53(36):9555-9. doi: 10.1002/anie.201405575. Epub 2014 Jul 15.

PMID:
25045110
15.

Palladium-catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with Michael acceptors: construction of vicinal quaternary stereocenters.

Khan A, Yang L, Xu J, Jin LY, Zhang YJ.

Angew Chem Int Ed Engl. 2014 Oct 13;53(42):11257-60. doi: 10.1002/anie.201407013. Epub 2014 Aug 28. Erratum in: Angew Chem Int Ed Engl. 2015 Jul 20;54(30):8584.

PMID:
25168969
16.

Radical asymmetric intramolecular α-cyclopropanation of aldehydes towards bicyclo[3.1.0]hexanes containing vicinal all-carbon quaternary stereocenters.

Ye L, Gu QS, Tian Y, Meng X, Chen GC, Liu XY.

Nat Commun. 2018 Jan 15;9(1):227. doi: 10.1038/s41467-017-02231-7.

17.

Catalytic Enantioselective Desymmetrization Reactions to All-Carbon Quaternary Stereocenters.

Zeng XP, Cao ZY, Wang YH, Zhou F, Zhou J.

Chem Rev. 2016 Jun 22;116(12):7330-96. doi: 10.1021/acs.chemrev.6b00094. Epub 2016 Jun 2. Review.

PMID:
27251100
18.

Isoindolinones as Michael Donors under Phase Transfer Catalysis: Enantioselective Synthesis of Phthalimidines Containing a Tetrasubstituted Carbon Stereocenter.

Scorzelli F, Di Mola A, Palombi L, Massa A.

Molecules. 2015 May 12;20(5):8484-98. doi: 10.3390/molecules20058484.

19.

Enantioselective Polyene Cyclization Catalyzed by a Chiral Brønsted Acid.

Fan L, Han C, Li X, Yao J, Wang Z, Yao C, Chen W, Wang T, Zhao J.

Angew Chem Int Ed Engl. 2018 Feb 19;57(8):2115-2119. doi: 10.1002/anie.201711603. Epub 2018 Feb 2.

PMID:
29316110
20.

Direct construction of vicinal all-carbon quaternary stereocenters in natural product synthesis.

Long R, Huang J, Gong J, Yang Z.

Nat Prod Rep. 2015 Nov;32(11):1584-601. doi: 10.1039/c5np00046g. Epub 2015 Sep 3. Review.

PMID:
26334685

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