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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
165 related items for PubMed ID: 32315097
1. Cu-Catalyzed Reductive gem-Difunctionalization of Terminal Alkynes via Hydrosilylation/Hydroamination Cascade: Concise Synthesis of α-Aminosilanes. Nishino S, Hirano K, Miura M. Chemistry; 2020 Jul 17; 26(40):8725-8728. PubMed ID: 32315097 [Abstract] [Full Text] [Related]
4. Asymmetric Synthesis of α-Aminoboronic Acid Derivatives by Copper-Catalyzed Enantioselective Hydroamination. Nishikawa D, Hirano K, Miura M. J Am Chem Soc; 2015 Dec 23; 137(50):15620-3. PubMed ID: 26653275 [Abstract] [Full Text] [Related]
5. Enantioselective Cu-catalyzed double hydroboration of alkynes to access chiral gem-diborylalkanes. Jin S, Li J, Liu K, Ding WY, Wang S, Huang X, Li X, Yu P, Song Q. Nat Commun; 2022 Jun 20; 13(1):3524. PubMed ID: 35725731 [Abstract] [Full Text] [Related]
12. Copper-Catalyzed Enantioselective Hydrosilylation of gem-Difluorocyclopropenes Leading to a Stereochemical Study of the Silylated gem-Difluorocyclopropanes. Sekine K, Akaishi D, Konagaya K, Ito S. Chemistry; 2022 Jun 07; 28(32):e202200657. PubMed ID: 35393679 [Abstract] [Full Text] [Related]
13. Copper-Catalyzed Regio- and Enantioselective Aminoboration of Unactivated Terminal Alkenes. Kato K, Hirano K, Miura M. Chemistry; 2018 Apr 17; 24(22):5775-5778. PubMed ID: 29512216 [Abstract] [Full Text] [Related]
14. Copper-Catalyzed Regiodivergent Asymmetric Difunctionalization of Terminal Alkynes. Wang S, Chen K, Niu J, Guo X, Yuan X, Yin J, Zhu B, Shi D, Guan W, Xiong T, Zhang Q. Angew Chem Int Ed Engl; 2024 Oct 21; 63(43):e202410833. PubMed ID: 38923633 [Abstract] [Full Text] [Related]
15. Copper-catalyzed regio- and enantioselective hydroamination of alkenes with hydroxylamines. Hesp KD. Angew Chem Int Ed Engl; 2014 Feb 17; 53(8):2034-6. PubMed ID: 24470434 [Abstract] [Full Text] [Related]