Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Huyi Zhang"'
Publikováno v:
Heliyon, Vol 10, Iss 1, Pp e23356- (2024)
Product innovation is a robust approach for enterprises to acquire and maintain a competitive edge. In order to support the development of enterprise product innovation, it is essential to establish an innovation pathway. Grounded in a modular perspe
Externí odkaz:
https://doaj.org/article/54ac353bec90481ebfd62125da3ee3d2
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0293309 (2023)
In order to advance civil aircraft manufacturing to higher levels, there is an urgent need to identify technological innovation opportunities to help new technology development. This paper first analyses the current state of the research field and de
Externí odkaz:
https://doaj.org/article/afbe44d963364671982be2ac3d352d53
Publikováno v:
Journal of Grey System. 2023, Vol. 35 Issue 3, p100-116. 17p.
Publikováno v:
Desalination & Water Treatment; 12/1/2023, Vol. 314, p330-338, 9p
Autor:
Kun Shen, Haitao Li, Huyi Zhang, Robert Lionberger, David Skanchy, Wei Song, Susan Rosencrance, Diandian Shen, Lawrence X. Yu
Publikováno v:
The AAPS Journal. 16:1132-1141
Under the Generic Drug User Fee Amendments (GDUFA) of 2012, Type II active pharmaceutical ingredient (API) drug master files (DMFs) must pay a user fee and pass a Completeness Assessment (CA) before they can be referenced in an Abbreviated New Drug A
Autor:
Sheila R. Whight, Nicolai A. Tvermoes, Tony Picking, Catherine Mader, Stephen A. Wring, Marquitta Warren, Stephen E. Schneider, Toivo E. Niemi, Paul E. Friedrich, Huyi Zhang, Peter Silinski, Brian L. Bray
Publikováno v:
Organic Process Research & Development. 12:101-110
TRI-999 is a HIV fusion inhibitory peptide designed to improve upon the efficacy and convenience of Enfuvirtide (ENF, Fuzeon), the first approved HIV entry inhibitor. Derived from a gp41 HR2 region partially overlapping the ENF sequence, TRI-999 is m
Publikováno v:
Helvetica Chimica Acta. 82:2037-2043
Novel oligonucleotide analogues built from isonucleosides were synthesized by the phosphoramidite approach on an automated DNA synthesizer. The phosphoramidite building blocks were synthesized by phosphitylation of the corresponding protected isonucl
Publikováno v:
Pure and Applied Chemistry. 71:1143-1146
Novel oligodeoxynucleotide analogues consisting of deoxyisonucleosides were obtained by the phosphoramidite approach on automated DNA-synthesizer. The phosphora- midite building blocks were synthesized by phosphorylation of corresponding isonucleosid
Publikováno v:
Carbohydrate Research. 318:157-161
Nucleophilic addition of KCN to 5-O-benzoyl-1,2-O-isopropylidene-α- d -erythro-pentofuranos-3-ulose gave the xylo cyanohydrin stereoselectively. Several xylos-3-yl-1,2,4-oxadiazole derivatives were synthesized from this cyanohydrin and were converte
Publikováno v:
Tetrahedron: Asymmetry. 9:141-149
3,5-O-Benzylidene-2-C-cyano-1,4-anhydro- l -xylitol 7 was synthesized stereoselectively from d -xylose in 7 steps. 2-C-(4-Aminocarbonyl-2-thiazoyl)-1,4-anhydro- l -xylitols and their fluoro derivatives were synthesized from the cyanohydrin 7. Fluorin