Synthesis of 7-Deaza-cyclic Adenosine-5′-diphosphate-carbocyclic-ribose and Its 7-Bromo Derivative as Intracellular Ca2+-Mobilizing Agents

2015 ◽  
Vol 80 (13) ◽  
pp. 6619-6627 ◽  
Author(s):  
Satoshi Takano ◽  
Takayoshi Tsuzuki ◽  
Takashi Murayama ◽  
Takashi Sakurai ◽  
Hayato Fukuda ◽  
...  
Keyword(s):  
1984 ◽  
Vol 49 (4) ◽  
pp. 1039-1050 ◽  
Author(s):  
Pavel Drašar ◽  
Vladimír Pouzar ◽  
Ivan Černý ◽  
Jorga Smolíková ◽  
Miroslav Havel

The protected 20(21)-en-20-ol ether III was oxidized with N-methylmorpholine N-oxide monohydrate and osmium tetroxide to give the hydroxy ketone IV which was converted into the bromo derivative VIII via the mesylate VI. Hantzsch reaction of the bromo ketone VIII with ethyl thioxamate afforded the thiazole XI whose hemisuccinate XIII and glycoside XV were prepared.


1999 ◽  
Vol 64 (6) ◽  
pp. 977-985 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Hans-Jörg Schanz ◽  
Wolfgang Milius ◽  
Catherine McCammon

Sodium hexaethyl-2,4-dicarba-nido-hexaborate(1-) (6), available from hexaethyl-2,4-dicarba- nido-hexaborane(8) (4) by deprotonation, reacts with deuterated methanol, CD3OD, to give back 4 without H/D exchange of the B-H-B hydrogen atom. The reaction of 6 with diethylboron chloride, Et2BCl, affords hexaethyl-2,4-dicarba-closo-hexaborane(6) (7), the first example of a peralkylated carborane of this type. In contrast, the reaction of 6 with boron tribromide, BBr3, leads mainly to 2,3,4,5,6,7-hexaethyl-2,4-dicarba-closo-heptaborane(7) (8), together with the corresponding 1-bromo derivative (9) and the closo-carborane 7 as side products. The reaction of two equivalents of 6 with FeCl2 gives the air-stable sandwich complex bis[hexaethyl-2,4-dicarba-nido-hexaborate(1-)]iron 10 which was characterised by X-ray structural analysis. All products were characterised by 1H, 11B and 13C NMR spectroscopy, and 57Fe Mössbauer spectroscopy was used to study 10.


Heterocycles ◽  
1988 ◽  
Vol 27 (1) ◽  
pp. 173 ◽  
Author(s):  
Francisco Fariña ◽  
M. Dolores Jim始ez ◽  
Raquel Ortega ◽  
Amelia Tito
Keyword(s):  

2014 ◽  
Vol 69 (8) ◽  
pp. 906-912 ◽  
Author(s):  
Michael Ritte ◽  
Clemens Bruhn ◽  
Ulrich Siemeling

The P,N-substituted ferrocene [Fe{η5-C5H4-P(S)Ph2}(η5-C5H4-NHCH2tBu)] was prepared in six steps from the bromo derivative [Fe{η5-C5H4-PPh2}(η5-C5H4-Br)]. Its reductive desulfurisation with Raney nickel afforded the corresponding phosphino-substituted derivative [Fe(η5-C5H4- PPh2)(η5-C5H4-NHCH2tBu)]. Both compounds have been structurally characterised by singlecrystal X-ray diffraction studies.


Polyhedron ◽  
2014 ◽  
Vol 67 ◽  
pp. 242-252 ◽  
Author(s):  
Éva A. Enyedy ◽  
Gabriella M. Bognár ◽  
Nóra V. Nagy ◽  
Tamás Jakusch ◽  
Tamás Kiss ◽  
...  

1978 ◽  
Vol 9 (5) ◽  
Author(s):  
MASAGI ODA ◽  
MITSUNORI ODA ◽  
S. MIYAKOSHI ◽  
Y. KITAHARA
Keyword(s):  

1984 ◽  
Vol 15 (6) ◽  
Author(s):  
J. P. FERNANDEZ ◽  
Y. ROBBE ◽  
J. P. CHAPAT ◽  
J. L. CHANAL ◽  
M. GENIN ◽  
...  

1983 ◽  
Vol 26 (9) ◽  
pp. 1317-1319 ◽  
Author(s):  
J. P. Fernandez ◽  
Y. Robbe ◽  
J. P. Chapat ◽  
J. L. Chanal ◽  
M. Genin ◽  
...  

1980 ◽  
Vol 33 (5) ◽  
pp. 1115 ◽  
Author(s):  
RD Allan ◽  
GAR Johnston ◽  
B Twitchin

Both trans and cis isomers of 4-amino-3-halogenobut-2-enoic acid have been prepared as potential irreversible inhibitors of the enzyme GABA- transaminase. trans-Addition of HX to 4-chlorobut-2-ynoic acid and subsequent amination gave the trans isomers (2; X = Cl, Br, I), while the key step in the synthesis of the cis isomers (3; X = Cl, Br) was the isomerization to cis-4-bromo-3-halogenobut-2-enoic acids during allylic bromination. The stereochemical assignments are supported by 1H and 13C n.m.r. spectral data. A convenient preparation of cis-4- aminobut-2-enoic acid by reduction of the bromo derivative is described, as well as the synthesis of 4-phthalimidobut-2-ynoic acid which is suitable for preparing radiolabelled GABA of high specific activity.


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