scholarly journals Superconductivity and cobalt oxidation state in metastableNaxCoO2−δ∙yH2O(x≈1∕3;y≈4x)

2005 ◽  
Vol 72 (13) ◽  
Author(s):  
P. Barnes ◽  
M. Avdeev ◽  
J. Jorgensen ◽  
D. Hinks ◽  
H. Claus ◽  
...  
2004 ◽  
Vol 412-414 ◽  
pp. 14-20 ◽  
Author(s):  
Kazunori Takada ◽  
Hiroya Sakurai ◽  
Eiji Takayama-Muromachi ◽  
Fujio Izumi ◽  
Ruben A. Dilanian ◽  
...  

2019 ◽  
Vol 123 (14) ◽  
pp. 9139-9145 ◽  
Author(s):  
Jun Chen ◽  
Qing Guo ◽  
Jiawei Wu ◽  
Wenshao Yang ◽  
Dongxu Dai ◽  
...  

2020 ◽  
Vol 124 (30) ◽  
pp. 16508-16514
Author(s):  
James L. White ◽  
Forrest S. Gittleson ◽  
Mark Homer ◽  
Farid El Gabaly

2010 ◽  
Vol 269 (2) ◽  
pp. 309-317 ◽  
Author(s):  
S. Zafeiratos ◽  
T. Dintzer ◽  
D. Teschner ◽  
R. Blume ◽  
M. Hävecker ◽  
...  

2003 ◽  
Vol 104 ◽  
pp. 289-292 ◽  
Author(s):  
R. Ortega ◽  
B. Fayard ◽  
M. Salomé ◽  
G. Devès ◽  
J. Susini

2019 ◽  
Author(s):  
Lars Gnägi ◽  
Severin Vital Martz ◽  
Daniel Meyer ◽  
Robin Marc Schärer ◽  
Philippe Renaud

<div><div><div><div><p>A very concise total synthesis of (+)-brefeldin C starting from 2-furanylcyclopentene is described. This approach is based on an unprecedented enantioselective radical hydroalkynylation process to introduce the two cyclopentane stereocenters in a single step. The use of a furan substituent allows to achieve a high trans diastereoselectivity during the radical process and it contains the four carbon atoms C1–C4 of the natural product in an oxidation state closely related to the one of the target molecule. The eight-step synthesis require six product purifications and it provides (+)-brefeldin C in 18% overall yield.</p></div></div></div></div>


2019 ◽  
Vol 16 (1) ◽  
pp. 173-180
Author(s):  
Mingwei Chen ◽  
Jinyu Hu ◽  
Xiaoli Tang ◽  
Qiming Zhu

Aim and Objective: The synthesis of bipyridines, especially 2, 2’-bipyridines, remains challenging because the catalytic cycle can be inhibited due to coordination of bipyridine to transition metal. Thus, the development of efficient methods for the synthesis of bipyridines is highly desirable. In the present work, we presented a promising approach for preparation of bipyridines via a Pd-catalyzed reductive homocoupling reaction with simple piperazine as a ligand. Materials and Methods: Simple and inexpensive piperazine was used as a ligand for Pd-catalyzed homocoupling reaction. The combination of Pd(OAc)2 and piperazine in dimethylformamide (DMF) was observed to form an excellent catalyst and efficiently catalyzed the homocoupling of azaarenyl halides, in which DMF was used as the solvent without excess reductants although stoichiometric reductant was generally required to generate the low-oxidation-state active metal species in the catalytic cycles. </P><P> Results: In this case, good to excellent yields of bipyridines and their (hetero) aromatic analogues were obtained in the presence of 2.5 mol% of Pd(OAc)2 and 5 mol% of piperazine, using K3PO4 as a base in DMF at 140°C. Conclusion: According to the results, piperazine as an inexpensive and efficient ligand was used in the Pd(OAc)2-catalyzed homocoupling reaction of heteroaryl and aryl halides. The coupling reaction was operationally simple and displayed good substrate compatibility.


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