Výsledky vyhledávání - "Young-Jo Lim"

Akademický článek

Insight into the Candidate Genes and Enriched Pathways Associated with Height, Length, Length to Height Ratio and Body-Weight of Korean Indigenous Breed, Jindo Dog Using Gene Set Enrichment-Based GWAS Analysis

Autor: Sunirmal Sheet, Jong-Seok Kim, Min-Jeong Ko, Na-Yeon Kim, Young-Jo Lim, Mi-Rim Park, Seung-Jin Lee, Jeong-Min Kim, Seok-Il Oh, Bong-Hwan Choi

Publikováno v: Animals, Vol 11, Iss 11, p 3136 (2021)

As a companion and hunting dog, height, length, length to height ratio (LHR) and body-weight are the vital economic traits for Jindo dog. Human selection and targeted breeding have produced an extraordinary diversity in these traits. Therefore, the i

Externí odkaz: https://doaj.org/article/a5e46d7a8ba04d8c90f38eca63f61ae0

Zobrazit plný text záznamu

Plný text ve formátu HTML

Enantioselective decarboxylative aldol addition of β-ketoacids to isatins catalyzed by binaphthyl-modified organocatalyst

Autor: Keon Woong Choi, Young Jo Lim, Chang Won Suh, Dae Young Kim, Chul Woo Chang

Publikováno v: Tetrahedron Letters. 54:3651-3654

The catalytic enantioselective decarboxylative aldol addition reaction of isatins with β-ketoacids promoted by chiral bifunctional organocatalysts have been developed, allowing facile synthesis of the corresponding chiral 3-hydroxy-3-phenacyloxindol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0bbc74809638941b5b61eeabaada0066
https://doi.org/10.1016/j.tetlet.2013.04.132

Zobrazit plný text záznamu

ChemInform Abstract: Enantioselective Direct α-Amination of Aromatic Ketones Catalyzed by Binaphthyl-Modified Primary Amine

Autor: Young Jo Lim, Dae Young Kim

Publikováno v: ChemInform. 44

Optically active α-aminated carbonyl compounds are important synthetic building blocks for the synthesis of a large number of biologically active compounds. The enantioselective electrophilic amination of carbonyl compounds represents a powerful and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::37484b4ba41bb1407f439bc942736f96
https://doi.org/10.1002/chin.201343063

Zobrazit plný text záznamu

ChemInform Abstract: Enantioselective Decarboxylative Aldol Addition of β-Ketoacids to Isatins Catalyzed by Binaphthyl-Modified Organocatalyst

Autor: Chang Won Suh, Keon Woong Choi, Young Jo Lim, Dae Young Kim, Chul Woo Chang

Publikováno v: ChemInform. 44

Optimized reaction conditions using a squaric acid diamide derivative as the catalyst are developed for the title reaction to afford phenacyloxindole derivatives with excellent enantioselectivity.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f11ac98516fb3b2ee76ad3283dd6af8c
https://doi.org/10.1002/chin.201342103

Zobrazit plný text záznamu

Enantioselective Direct α-Amination of Aromatic Ketones Catalyzed by Binaphthyl-Modified Primary Amine

Autor: Young Jo Lim, Dae Young Kim

Publikováno v: Bulletin of the Korean Chemical Society. 34:1955-1956

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a421f095204578cbbc2ca05cb9cc795b
https://doi.org/10.5012/bkcs.2013.34.7.1955

Zobrazit plný text záznamu

Enantioselective Conjugate Addition of 4-Hydroxycoumarin to Enones Catalyzed by Binaphthyl-Modified Primary Amine Organocatalyst

Autor: Dae Young Kim, Young Jo Lim

Publikováno v: Bulletin of the Korean Chemical Society. 33:1825-1826

The Michael addition reaction is widely recognized as one of the most general methods for formation of C-C bonds in organic synthesis, and the development of enantioselective catalytic conjugate addition reaction has been subject of intensive researc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::62278f18be06a8c6ddb833a57a065dad
https://doi.org/10.5012/bkcs.2012.33.6.1825

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání