Synthesis and characterization of novel kinds of polyethylene oxide drugs containing 5-fluorouracil and nitrogen mustard at one end and 4-amino-N-(2-pyrimidinyl) benzene sulfonamide at the other end

2000 ◽  
Vol 36 (8) ◽  
pp. 1703-1710 ◽  
Author(s):  
Sheng Chen ◽  
Zhaohua Huang ◽  
Junlian Huang
2021 ◽  
Vol 77 (3) ◽  
pp. 152-160
Author(s):  
Philipp Honegger ◽  
Alexander Roller ◽  
Michael Widhalm

In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(FcA)2(Ph)P], one of which contains four stereogenic centres (two C chiral and two planar chiral centres), i.e. 1,1′-(phenylphosphanediyl)bis{(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocene}, [Fe2(C5H5)2(C24H25O4P)], and the other phosphine sulfide is a purely planar–chiral compound (two planar chiral centres), i.e. bis[(2S p)--2-ethenylferrocen-1-yl]phenylphosphane sulfide, [Fe2(C5H5)2(C20H17PS)]. Owing to the stereocentres present, reactions performed on [(FcA)2(Ph)P]-type compounds strongly favour one ferrocene unit over the other due to diastereoselectivity. Furthermore, we present four related structures where the ferrocene units are not identical [(FcA)(FcB)(Ph)P]. These are {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C22H21O2PS)], [(2S p)-2-ethenylferrocen-1-yl]{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C20H19OPS)], {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(R)-phosphine sulfide, [Fe2(C5H5)2(C22H23O3PS)], and {(2S p)-2-[(1R)-1-benzylamino)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C27H26NPS)]. All of the structures are accessible in one step from known precursors.


2019 ◽  
Vol 238 ◽  
pp. 58-61 ◽  
Author(s):  
Jamie A.G. Hamilton ◽  
Andrew Ozarowski ◽  
Edikan Archibong ◽  
Sylvia Thomas ◽  
William Serrano-Garcia ◽  
...  

2010 ◽  
Vol 305-306 ◽  
pp. 89-94
Author(s):  
A. Samadi Maybodi ◽  
S.K. Hassani Nejad-Darzi

Zinc phosphate molecular sieve were synthesized using zinc chloride, phosphoric acid as a zinc and phosphor source, respectively. Different types of zinc phosphates zeolites were synthesized by conventional hydrothermal (using (2-hydroxyethyl) trimethylammonium hydroxide (2-HETMAOH) as new template. Also, ethylene glycol (EG) was utilized as co-solvent and ultrasonic tool was applied as mixer. The influence of the chemical composition of the starting sol-gel and the other parameters such as, Zn/P mole ratio, time of microwave irradiation were studied.


2019 ◽  
Vol 75 (7) ◽  
pp. 872-876
Author(s):  
Lukáš Krivosudský ◽  
Alexander Roller ◽  
Annette Rompel

The monovanadium-substituted polyoxometalate anion [VMo7O26]5−, exhibiting a β-octamolybdate archetype structure, was selectively prepared as pentapotassium [hexaikosaoxido(heptamolybdenumvanadium)]ate hexahydrate, K5[VMo7O26]·6H2O (VMo7 ), by oxidation of a reduced vanadomolybdate solution with hydrogen peroxide in a fast one-pot approach. X-ray structure analysis revealed that the V atom occupies a single position in the cluster that differs from the other positions by the presence of one doubly-bonded O atom instead of two terminal oxide ligands in all other positions. The composition and structure of VMo7 was also confirmed by elemental analyses and IR spectroscopy. The selectivity of the synthesis was inspected by a 51V NMR investigation which showed that this species bound about 95% of VV in the crystallization solution. Upon dissolution of VMo7 in aqueous solution, the [VMo7O26]5− anion is substantially decomposed, mostly into [VMo5O19]3−, α-[VMo7O26]4− and [V2Mo4O19]4−, depending on the pH.


2006 ◽  
Vol 17 (21) ◽  
pp. 5417-5422 ◽  
Author(s):  
Kalpana Awasthi ◽  
Seema Awasthi ◽  
Anchal Srivastava ◽  
R Kamalakaran ◽  
S Talapatra ◽  
...  

1987 ◽  
Vol 42 (5) ◽  
pp. 599-604 ◽  
Author(s):  
Rainer Mattes ◽  
Heinz Scholand ◽  
Ulrich Mikloweit ◽  
Volker Schrenk

transThe reaction of NH2NHC(S)OR, (R = Me, Et) with MoO2(acac)2 yields the dimeric complexes MO2O3(MeC(O)CHC(Me)NNC(S)0R)2 (1) with the planar O = Mo - O - Mo = O group. The tetradentate O,N,S-donor ligand is formed through condensation of acetylacetone with the organohydrazine. The reactions of NH2NHC(S)OMe with MoO2(S2CNEt2)2 and MoO2(ONEt2)2 give the diazenido hydrazido complexes Mo(NNC(S)OMe)(NH2NC(S)OMe)(S2CNEt2)2·CH2Cl2(2) and Mo(NNC(S)OMe)(NH2NC(S)OMe)2(ONEt2) (4). The metal atoms in both compounds are seven coordinated and contain the approximately linear diazenido ligand NNC(S)OMe and one (2) or two (4) N,S-chelating hydrazido(1-) ligands NH2NC(S)OMe. 2 has crystallographically imposed mirror symmetry. Recrystallization of 2 from toluene in air gives the asymmetric dinuclear complex (Et2NCS2)(O)Mo(μ-NNC(S)OMe)2Mo(S2CNMe2) (3). The Mo-Mo distance is 267.0(2) pm. One Mo site has square pyramidal MoOS2N2 geometry, the other trigonal prismatic MoN2S4 geometry. The coordination of the bridging N atoms is slightly pyramidal. The compounds 1, 2 and 3 have been further characterized by vibrational spectroscopy.


Sign in / Sign up

Export Citation Format

Share Document