Acceptorless Dehydrogenative Cyclization of o-Aminobenzyl Alcohols with Ketones to Quinolines in Water Catalyzed by Water-Soluble Metal–Ligand Bifunctional Catalyst [Cp*(6,6′-(OH)2bpy)(H2O)][OTf]2

2016 ◽  
Vol 18 (15) ◽  
pp. 3558-3561 ◽  
Author(s):  
Rongzhou Wang ◽  
Hongjun Fan ◽  
Wei Zhao ◽  
Feng Li
2002 ◽  
Vol 4 (14) ◽  
pp. 2361-2363 ◽  
Author(s):  
Takeyuki Suzuki ◽  
Kenji Morita ◽  
Mika Tsuchida ◽  
Kunio Hiroi

2019 ◽  
Vol 43 (27) ◽  
pp. 10755-10762 ◽  
Author(s):  
Yao Ai ◽  
Pengcheng Liu ◽  
Ran Liang ◽  
Yan Liu ◽  
Feng Li

A water-soluble dinuclear Cp*Ir complex bearing 4,4′,6,6′-tetrahydroxy-2,2′-bipyrimidine as a bridging ligand was found to be a highly effective catalyst for the N-alkylation of ketones with alcohols in water.


2010 ◽  
Vol 29 (17) ◽  
pp. 3896-3900 ◽  
Author(s):  
Liza Koren-Selfridge ◽  
Ian P. Query ◽  
Joel A. Hanson ◽  
Nicholas A. Isley ◽  
Ilia A. Guzei ◽  
...  

Tetrahedron ◽  
2019 ◽  
Vol 75 (34) ◽  
pp. 130463
Author(s):  
Rongzhou Wang ◽  
Jipeng Qi ◽  
Yuancheng Yue ◽  
Zhe Lian ◽  
Haibin Xiao ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (48) ◽  
pp. no-no
Author(s):  
Takeyuki Suzuki ◽  
Kenji Morita ◽  
Mika Tsuchida ◽  
Kunio Hiroi

Author(s):  
J. G. Robertson ◽  
D. F. Parsons

The extraction of lipids from tissues during fixation and embedding for electron microscopy is widely recognized as a source of possible artifact, especially at the membrane level of cell organization. Lipid extraction is also a major disadvantage in electron microscope autoradiography of radioactive lipids, as in studies of the uptake of radioactive fatty acids by intestinal slices. Retention of lipids by fixation with osmium tetroxide is generally limited to glycolipids, phospholipids and highly unsaturated neutral lipids. Saturated neutral lipids and sterols tend to be easily extracted by organic dehydrating reagents prior to embedding. Retention of the more saturated lipids in embedded tissue might be achieved by developing new cross-linking reagents, by the use of highly water soluble embedding materials or by working at very low temperatures.


Author(s):  
J. D. McLean ◽  
S. J. Singer

The successful application of ferritin labeled antibodies (F-A) to ultrathin sections of biological material has been hampered by two main difficulties. Firstly the normally used procedures for the preparation of material for thin sectioning often result in a loss of antigenicity. Secondly the polymers employed for embedding may non-specifically absorb the F-A. Our earlier use of cross-linked polyampholytes as embedding media partially overcame these problems. However the water-soluble monomers used for this method still extract many lipids from the material.


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