Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nguyen Thai Hung"'
Autor:
Tran, Minh-Phuong, Nguyen, Thanh-Nhan, Nguyen, Thai-Hung, Nguyen, Tan-Phuc, Nguyen, Tien-Khai, Nguyen, Cong-Duy-Nguyen, Huynh, Trung-Hieu
In this paper, we study a new approach related to the convergence analysis of Ishikawa-type iterative models to a common fixed point of two non-expansive mappings in Banach spaces. The main novelty of our contribution lies in the so-called \emph{opti
Externí odkaz:
http://arxiv.org/abs/2401.02093
Autor:
NGUYEN THAI HUNG, 阮泰興
102
The internet explosion has opened the door to a new electronic world. Consumers are now able to use the Internet for a variety of purposes such as research, communication, online banking, and even shopping. The Internet is rapidly becoming a
The internet explosion has opened the door to a new electronic world. Consumers are now able to use the Internet for a variety of purposes such as research, communication, online banking, and even shopping. The Internet is rapidly becoming a
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/19926865702645724860
Publikováno v:
Journal of Computer Science and Cybernetics. 1:16-19
Publikováno v:
Journal of Computer Science and Cybernetics. 4:17-18
Autor:
Rasheed Ahmad Khera, Holger Feist, Nguyen Thai Hung, Peter Langer, Munawar Hussain, Nadi Eleya, Alexander Villinger
Publikováno v:
Helvetica Chimica Acta. 95:469-482
SuzukiMiyaura reactions of 2,3-dibromo-1H-inden-1-one afforded a wide range of arylated 1H-inden-1-ones. Sonogashira cross-coupling reactions gave alkynylated indenones. The reactions proceeded with very good regioselectivity in the less sterically h
Publikováno v:
Tetrahedron Letters. 52:184-187
The first transition metal-catalyzed cross-coupling reactions of 2,3-dibromo-1H-inden-1-one are reported. The Suzuki–Miyaura reaction of 2,3-dibromo-1H-inden-1-one with 2 equiv of arylboronic acid gave 2,3-diaryl-1H-inden-1-ones. The reaction with
Publikováno v:
Org. Biomol. Chem.. 9:370-373
Suzuki-Miyaura reactions of 2,3,4,5-tetrabromofuran allow a convenient and site-selective synthesis of mono-, di- and tetraarylfurans which are not readily available by other methods.
Autor:
Dhafer Saber Zinad, Peter Langer, Rasheed Ahmad Khera, Munawar Hussain, Imran Malik, Nguyen Thai Hung
Publikováno v:
Advanced Synthesis & Catalysis. 352:1429-1433
Suzuki―Miyaura reactions of 2,4,5,6-tetra-chloropyrimidine allow a convenient synthesis of mono-, di-, tri- and tetraarylpyrimidines which are not readily available by other methods. All reactions proceed with excellent site-selectivity.
Autor:
Alexander Villinger, Peter Langer, Rasheed Ahmad, Muhammad Sher, Abdolmajid Riahi, Ihsan Ullah, Rasheed Ahmad Khera, Christine Fischer, Nguyen Thai Hung
Publikováno v:
Tetrahedron. 66:1643-1652
Functionalized triarylmethanes are prepared in two steps by FeCl 3 -catalyzed benzylation of acetylacetone to give 3-(diarylmethyl)pentane-2,4-diones and subsequent formal [3+3] cyclization of the latter with 1,3-bis(trimethylsilyloxy)-1,3-dienes.
Publikováno v:
Tetrahedron Letters. 50:3929-3932
Functionalized dibenzofurans were prepared based on domino ’twofold Heck/6π-electrocyclization’ reactions of 2,3-di- and 2,3,5-tribromobenzofuran.