Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Fu-Qiang Bi"'
1
Akademický článek
A Family of Energetic Materials Based on 1,2,4-Oxadiazole and 1,2,5-Oxadiazole Backbones With Low Insensitivity and Good Detonation Performance
Autor: Qi Xue, Fu-qiang Bi, Jun-lin Zhang, Zi-jun Wang, Lian-jie Zhai, Huan Huo, Bo-zhou Wang, Sheng-yong Zhang
Publikováno v: Frontiers in Chemistry, Vol 7 (2020)
Design and synthesis of new compounds with both high detonation performances and good safety properties have always been a formidable task in the field of energetic materials. By introducing -ONO2 and -NHNO2 moieties into 1,2,4-oxadiazole- and 1,2,5-
Externí odkaz: https://doaj.org/article/3346486174224aaaa9f245fbf3d00bb8
Zobrazit plný text záznamu
2
Akademický článek
Synthesis of Energetic 7-Nitro-3,5-dihydro-4H-pyrazolo[4,3-d][1,2,3]triazin-4-one Based on a Novel Hofmann-Type Rearrangement
Autor: Fu-Qiang Bi, Yi-Fen Luo, Jun-Lin Zhang, Huan Huo, Bo-Zhou Wang
Publikováno v: Molecules, Vol 26, Iss 23, p 7319 (2021)
Rearrangement reactions are efficient strategies in organic synthesis and contribute enormously to the development of energetic materials. Here, we report on the preparation of a fused energetic structure of 7-nitro-3,5-dihydro-4H-pyrazolo[4,3-d][1,2
Externí odkaz: https://doaj.org/article/24e0bdc21c4442b4983b8cff07cbe9cf
Zobrazit plný text záznamu
7
First total synthesis of 10α-hydroxy-4-muurolen-3-one and its C10-isomer
Autor: Fu Qiang Bi, Yu Lin Li, Chen Xi Zhang, Li Jing Fang
Publikováno v: Chinese Chemical Letters. 19:1265-1267
An efficient synthetic route to muurolane type sesquiterpenes starting from ( R )-carvone, employing allylic diazene rearrangement and the ring closing methesis (RCM) reaction as key steps, is described. The first asymmetric total synthesis of (−)-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d37b18780f3c9b6c481efff5ba18f9cf
https://doi.org/10.1016/j.cclet.2008.09.022
Zobrazit plný text záznamu
8
A simple and efficient synthesis of the valsartan
Autor: Fu Qiang Bi, Guo Jun Zheng, Chen Xi Zhang, Yulin Li
Publikováno v: Chinese Chemical Letters. 19:759-761
Valsartan 1, one of the most important agents used in antihypertensive therapy today, was synthesized starting from l -valin methyl ester hydrochloride 2 through four steps in an overall yield of 60%. The key step involves the palladium-catalyzed Suz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0e1b578bdf77355f784c5ed29aff7f64
https://doi.org/10.1016/j.cclet.2008.04.032
Zobrazit plný text záznamu
9
An enantioselective formal synthesis of (−)-thujopsene
Autor: Chen Xi Zhang, Fu Qiang Bi, Yulin Li, Li Jing Fang
Publikováno v: Chinese Chemical Letters. 19:256-258
Dihydromayurone (3), a key intermediate to synthesize (−)-thujopsene (1), was efficient enantiocontrolled synthesized from (+)-dihydrocarvone through 9 steps in an overall yield of 19.3%. The key step was the Simmons–Smith reaction.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1761b98f1123f02b10e60f0aa97f1201
https://doi.org/10.1016/j.cclet.2008.01.009
Zobrazit plný text záznamu
10
The first total synthesis of ligudentatin A
Autor: Chen Xi Zhang, Yulin Li, Fu Qiang Bi
Publikováno v: Chinese Chemical Letters. 19:805-806
Ligudentatin A 1, a new phenolic norsesquiterpenes, was first synthesized starting from (+)-perillaldehyde 3 through five steps, successively, in an overall yield of 20.8%. The key steps were the Diels–Alder reaction and aromatization of enone to p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::48d3fd7f0f3526d2d1b3ca8a162d9a65
https://doi.org/10.1016/j.cclet.2008.04.037
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje