Pivnitsky Kazimir Konstantinovich

Publications in Math-Net.Ru

1. Lamellar conglomerates
   
   Mendeleev Commun., 30:1 (2020),  1–6
2. Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins
   
   Mendeleev Commun., 29:4 (2019),  372–374
3. Racemic estrone methyl ether is the lamellar conglomerate
   
   Mendeleev Commun., 29:3 (2019),  256–259
4. Oxidative C–O coupling as a new idea in the ‘click-like chemistry’: malonyl peroxides for the conjugation of two molecules
   
   Mendeleev Commun., 29:2 (2019),  132–134
5. Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity
   
   Mendeleev Commun., 28:5 (2018),  505–507
6. Spontaneous reaction of malonyl peroxides with methanol
   
   Mendeleev Commun., 27:3 (2017),  243–245
7. Side-modified 15-deoxy-Δ^12,14-prostaglandin D₂, precursor of corresponding PGJ₂. Synthesis from cloprostenol and anticancer activity
   
   Mendeleev Commun., 27:2 (2017),  125–127
8. Alcoholysis of malonyl peroxides to give peracids
   
   Mendeleev Commun., 26:1 (2016),  14–15
9. Facile reaction of bis(tri-n-butyltin) oxide with silica gel
   
   Mendeleev Commun., 25:1 (2015),  51–53
10. A convenient synthesis of cyclopropane malonyl peroxide
    
    Mendeleev Commun., 24:6 (2014),  345
11. Unexpected fragmentation of 16β-acetoxy-22-oxocholestanes on the action of methylenetriphenylphosphorane
    
    Mendeleev Commun., 24:5 (2014),  272–273
12. Potassium fluoride on calcium fluoride – a practical reagent for removal of organotin residues from reaction mixtures
    
    Mendeleev Commun., 23:5 (2013),  257–259
13. Pyridinium o-iodoxybenzoate as a Safe form of a Famous Oxidant
    
    Mendeleev Commun., 22:3 (2012),  129–131
14. Practical synthesis of 16,22-diketocholesterol acetate, a precursor of anticancer saponin OSW-1, from diosgenin
    
    Mendeleev Commun., 20:6 (2010),  318–320
15. o-Iodoxybenzoic acid in dimethylformamide as a convenient reagent for the oxidation of alcohols to aldehydes and ketones
    
    Mendeleev Commun., 18:6 (2008),  309–311
16. Enantiomeric NMR analysis of chiral epoxides as addition compounds with d-ephedrine
    
    Mendeleev Commun., 15:5 (2005),  175–178
17. Total synthesis of trioxilins 11,12-threo-(8,11,12)-A₃ through type B₃ trioxilins
    
    Mendeleev Commun., 14:6 (2004),  291–293
18. Enantiodivergent total synthesis of trioxilins B₃ using Sharpless asymmetric olefin dihydroxylation
    
    Mendeleev Commun., 14:6 (2004),  287–290
19. Synthesis of series 2 trioxilins from trioxilin B₃ by selective hydrogenation
    
    Mendeleev Commun., 10:4 (2000),  130–131
20. Enantiomeric NMR analysis of organic acids with the Corey chiral controller
    
    Mendeleev Commun., 9:4 (1999),  149–151
21. Synthesis of a photoaffinic hepoxilin analog
    
    Mendeleev Commun., 7:3 (1997),  90–91
22. Synthesis of trioxilins B₃ from hepoxilins B₃
    
    Mendeleev Commun., 6:6 (1996),  251–252
23. Total synthesis of 20-hydroxy-hepoxilins, new metabolites of the hepoxilin family
    
    Mendeleev Commun., 6:4 (1996),  130–132
24. A new method of synthesizing 2,2,6,6-tetraalkyltetrahydropyrandiones-3,5
    
    Dokl. Akad. Nauk SSSR, 132:1 (1960),  127–129