Liu R - Search Results

1

Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold.

Shi RG, Wang XH, Liu R, Yan CG. Shi RG, et al. Among authors: liu r. Chem Commun (Camb). 2016 May 7;52(37):6280-3. doi: 10.1039/c6cc00525j. Epub 2016 Apr 15. Chem Commun (Camb). 2016. PMID: 27079548

2

Molecular diversity of the domino annulation reaction of 2-aryl-3-nitrochromenes with pivaloylacetonitriles.

Jiang W, Sun J, Liu RZ, Yan CG. Jiang W, et al. Org Biomol Chem. 2018 Aug 15;16(32):5816-5822. doi: 10.1039/c8ob01504j. Org Biomol Chem. 2018. PMID: 30066005

3

Diastereoselective construction of carbazole-based spirooxindoles via the Levy three-component reaction.

Zhan SC, Sun J, Liu RZ, Yan CG. Zhan SC, et al. Org Biomol Chem. 2019 Dec 18;18(1):163-168. doi: 10.1039/c9ob02013f. Org Biomol Chem. 2019. PMID: 31808499

4

Domino Reaction of Aromatic Aldehydes and 1,3-Indanediones for Construction of Bicyclo[2.2.2]octanes and Dibenzo[b,g]indeno[1',2':3,4]fluoreno[1,2-d]oxonines.

Cao J, Shi RG, Sun J, Liu D, Liu R, Xia X, Wang Y, Yan CG. Cao J, et al. Among authors: liu r, liu d. J Org Chem. 2020 Feb 21;85(4):2168-2179. doi: 10.1021/acs.joc.9b02911. Epub 2020 Jan 10. J Org Chem. 2020. PMID: 31876418

5

Highly selective hydrosilylation of equilibrating allylic azides.

Liu R , Wei Z , Wang J , Liu Y , Xue H . Liu R , et al. Among authors: liu y. Chem Commun (Camb). 2020 May 7;56(37):5038-5041. doi: 10.1039/d0cc01316a. Epub 2020 Apr 3. Chem Commun (Camb). 2020. PMID: 32242569

6

Convergent Synthesis of Triindanone-Fused Spiro[bicyclo[2.2.2]octane-2,3'-indolines] via Domino Reaction of 1,3-Indanedione and 3-Methyleneoxindoles.

Liu D, Cao J, Sun J, Liu RZ, Yan CG. Liu D, et al. Org Lett. 2020 Nov 20;22(22):8931-8936. doi: 10.1021/acs.orglett.0c03331. Epub 2020 Nov 9. Org Lett. 2020. PMID: 33166154

7

Diastereoselective Synthesis of Tetrahydrospiro[carbazole-1,3'-indolines] via an InBr₃-Catalyzed Domino Diels-Alder Reaction.

Wang D, Sun J, Liu RZ, Wang Y, Yan CG. Wang D, et al. J Org Chem. 2021 Apr 16;86(8):5616-5629. doi: 10.1021/acs.joc.1c00103. Epub 2021 Apr 5. J Org Chem. 2021. PMID: 33818095

8

Selective hydroboration of equilibrating allylic azides.

Liu R, Zhang Y, Xu J. Liu R, et al. Chem Commun (Camb). 2021 Sep 6;57(71):8913-8916. doi: 10.1039/d1cc02520a. Chem Commun (Camb). 2021. PMID: 35225991

9

Stereocontrol in an intermolecular Schmidt reaction of equilibrating hydroxyalkyl allylic azides.

Liu R, Wang J, Wu H, Quan X, Wang S, Guo J, Wang Y, Li H. Liu R, et al. Chem Commun (Camb). 2024 Apr 16;60(32):4362-4365. doi: 10.1039/d4cc00907j. Chem Commun (Camb). 2024. PMID: 38563154

10

Sterically-controlled intermolecular Friedel-Crafts acylation with twisted amides via selective N-C cleavage under mild conditions.

Liu Y, Meng G, Liu R, Szostak M. Liu Y, et al. Among authors: liu r. Chem Commun (Camb). 2016 May 21;52(41):6841-4. doi: 10.1039/c6cc02324j. Epub 2016 May 3. Chem Commun (Camb). 2016. PMID: 27139813

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