scholarly journals Evolution of Strain in Heteroepitaxial Cadmium Carbonate Overgrowths on Dolomite

2018 ◽  
Vol 18 (5) ◽  
pp. 2871-2882 ◽  
Author(s):  
Erika Callagon La Plante ◽  
Peter J. Eng ◽  
Sang Soo Lee ◽  
Neil C. Sturchio ◽  
Kathryn L. Nagy ◽  
...  
Keyword(s):  
2020 ◽  
Vol 109 ◽  
pp. 110295
Author(s):  
S.G. Ruvalcaba-Manzo ◽  
S.J. Castillo ◽  
R. Ochoa-Landín ◽  
M. Flores-Acosta ◽  
R. Ramírez-Bon

Author(s):  
Tse-Lok Ho ◽  
Mary Fieser ◽  
Louis Fieser
Keyword(s):  

Langmuir ◽  
2005 ◽  
Vol 21 (16) ◽  
pp. 7220-7224 ◽  
Author(s):  
Ambarish Sanyal ◽  
Debabrata Rautaray ◽  
Vipul Bansal ◽  
Absar Ahmad ◽  
Murali Sastry

2017 ◽  
Vol 205 ◽  
pp. 360-380 ◽  
Author(s):  
Erika Blanca R. Callagon ◽  
Sang Soo Lee ◽  
Peter J. Eng ◽  
Nouamane Laanait ◽  
Neil C. Sturchio ◽  
...  

2020 ◽  
Vol 246 ◽  
pp. 122797
Author(s):  
C.M. Martínez ◽  
M. Rivera-Hernández ◽  
Luis H. Álvarez ◽  
Ismael Acosta-Rodríguez ◽  
F. Ruíz ◽  
...  

1993 ◽  
Vol 46 (5) ◽  
pp. 713 ◽  
Author(s):  
KA Byriel ◽  
LR Gahan ◽  
CHL Kennard ◽  
JL Latten ◽  
PC Healy

Reaction of cadmium carbonate with 1,4,7,10-tetraoxa-13-azacyclopentadecane-13-acetic acid (HL4) in warm aqueous solution results in the isolation of crystals of the tetrameric cluster [Cd4(L4)4] [CdCl4]2.3H2O, an ordered assembly of acetate-bridged macrocyclic species. The crystals are triclinic, space group Pī with a 15.67(3), b 16.90(2), c 17.92(3) Ǻ, α 101.41(4), β 115.57(7), γ 102.23(8)°. R was 0.045 for 7191 [I > 2.5σ(I)] reflections.


2008 ◽  
Vol 59 (1) ◽  
pp. 52-55
Author(s):  
Nicoleta Florentina Predescu ◽  
Silvia Iga ◽  
Alina Nicolescu ◽  
Dumitru Petru Iga

Galactofuranosylation has been accomplished with 1-bromo-1-deoxy-2,3,5,6-tetra-O-benzoyl-a-D-galactofuranoside in the presence of cadmium carbonate as promotor. Glycosylation agent has been prepared by bromination of penta-O-benzoyl-ab-D-galactofuranoside with a solution of hydrogen bromide in glacial acetic acid. The precursor of the latter reaction has been produced by benzoylation of D-galactose that had been heated in pyridine while still warm. The following hydroxysteroids have been selected as being representative in terms of configuration, type of hybridization of carbon bearing hydroxyl, position on cyclopentenoperhydrophenantrene nucleus and, implicitly, the degree of shielding: estrone, androstanolone, 11-a-hydroxyprogesterone, prednisolone. The synthesized galactofuranosides have been characterized by 1H and 13C NMR as well as by chromatographic and chemical means.


1965 ◽  
Vol 43 (8) ◽  
pp. 2345-2356 ◽  
Author(s):  
W. A. Szarek ◽  
J. K. N. Jones

Lead tetraacetate oxidation of 6-acetamido-6-deoxy-D-galactose (IX) yielded a syrup which was converted to a compound formulated as 4-acetamido-4-deoxy-1,2-O-isopropylidene-D-threofuranose (XII). The same syrup was obtained by alkaline degradation of the product of oxidation of 5-acetamido-5-deoxy-D-xylose diethyl dithioacetal (XVII) with peroxypropionic acid. Treatment of compound XII with p-toluenesulfonyl chloride yielded crystalline 4-acetamido-4-deoxy-1,2-O-isopropylidene-3-O-p-tolylsufonyl-D-threofuranose (XIII).Demercaptalation of 6-acetamido-2,3,4,5-tetra-O-acetyl-6-deoxy-D-galactose diethyl dithioacetal (XX) with mercuric chloride and cadmium carbonate in aqueous acetone did not yield a nitrogen-containing septanose ring but an acyclic derivative.


1978 ◽  
Vol 13 (1) ◽  
pp. 226-229 ◽  
Author(s):  
K. Satyanarayana Murthy ◽  
K. V. Krishna Rao

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