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Palladium-catalyzed stereoselective hydrostannation of substituted propargyl alcohols with trineophyltin hydride
(Elsevier Science Sa, 2008-05)
This paper reports results obtained in a study on the palladium-catalyzed hydrostannation of substituted propargyl alcohols with the bulky trineophyltin hydride (1). The reaction of 1 with 10 propargyl alcohols containing ...
Bicyclic allyltin derivatives through selective "one pot" hydrostannation - Diels-Alder reaction
(Arkat, 2011-02)
In this paper we report a simple "one pot" procedure to functionalized allyltin derivatives from 1- ethynylcyclohexene. Radical addition of trineophyltin hydride gives quantitatively to (Z,E)-1-(2- trineophylstannylvinyl ...
Stereoselective Synthesis of Stannyl Enones via Palladium-Catalyzed and Free Radical Hydrostannation of Alkynyl Ketones with Trineophyltin Hydride
(American Chemical Society, 2003-12)
A study on the addition of trineophyltin hydride (1) to alkynones under free radical (AIBN and Et3B) and palladium-catalyzed [(PPh3) 2PdCl2] conditions is reported. The results obtained indicate that the addition of 1 to ...
Stereoselective hydrostannation of substituted alkynes initiated by triethylborane and reactivity of bulky triorganotin hydrides
(Elsevier Science Sa, 2006-03)
This paper reports the results obtained in a study on the radical hydrostannation of mono- and disubstituted alkynes with bulky triorganotin hydrides using triethylborane as initiator. The addition of trineophyl- (1), ...
Stereoselective hydrostannation of substituted alkynes with trineophyltin hydride
(Elsevier Science Sa, 2002-05)
Hydrostannation of mono- and disubstituted alkynes with trineophyltin hydride (1) leads to vinylstannes in good to excellent yields the configuration of the products depending on the reaction conditions. Thus, whereas ...
Stereoselective radical tandem cyclohydrostannation of optically active di-unsaturated esters of TADDOL
(American Chemical Society, 2008-02)
This paper reports the results obtained in a study on the radical addition of triorganotin hydrides, R3SnH (R = Me, n-Bu, Ph; Neophyl), to four TADDOL unsaturated diesters. It was found that diese reactions lead in high ...
Synthesis, characterization and antifungal assessment of optically active bis-organotin compounds derived from (S)-BINOL diesters
(Bentham Science Publishers, 2019-05)
Background: Organotin(IV) derivatives have appeared recently as potential biologically active metallopharmaceuticals exhibiting a variety of therapeutic activities. Hence, it is important to study the synthesis of new ...
Synthesis of organotin derivatives of optically active eleven-membered macrodiolides
(Pergamon-Elsevier Science Ltd, 2016-05-01)
The synthesis and the results obtained in the hydrostannation of eight new TADDOL diacrylates and methacrylates are reported. The addition of triorganotin hydrides, R3SnH, 12-14 (R = nBu, neophyl, Ph, respectively) to ...