机译:Aminolysis ofP‐trichloro‐N‐dichlorophosphorylmonophosphazene and the crystal structure of 1‐(dichlorophosphinyl)‐2‐chloro‐2,2‐bis(diisopropylamino)phosphazene
机译:Substitution reactions at silicon under strongly acidic conditions: Ligand metathesis between methyltrichlorosilane and octamethylcyclotetrasiloxane
机译:Carbapenem antibiotics: Displacement of C‐3 sulfur side chain by another thiol moiety, and quaternization of a weaker pyridine nitrogen over a stronger primary amine (preparation of BMY 40732 and BMY 40886)
机译:Low‐temperature1H,13C,77Se, and125Te NMR studies on the apical‐apical ligand exchange via the hypervalent tellurium and selenium ate complexes 10‐M‐3(C3); M = Se, Te in the reactions of diaryl tellurides and selenides with aryllithium reagents
机译:Conformational properties of cyclic pentaalkoxy phosphoranes: Apical–equatorial attachment and nonchair conformation of the phosphorus‐containing six‐membered ring
机译:Electron distribution in 1‐organo‐1H‐tetrazole‐5‐thiols. Crystal and molecular structure of 1‐methyl‐1H‐tetrazole‐5‐thioland its potassium (18‐crown‐6) salt
机译:The isomerization/chlorination of 0,0‐dialkyl methylthiophosphonates with phosphorus oxychloride—a new convenient synthesis of S‐alkyl methylthiophosphonic acid derivatives
机译:Investigation of the mechanism of reaction ofS‐ethyl‐N,N′‐tetraethyldiamidothio‐phosphite with C5H5Mn(CO)2NO+BF 4−by fourier transform infrared spectroscopy
机译:Stereoselective sulfur extrusion reaction ofsyn‐ andanti‐10,20‐dibromo‐2,3,12,13‐tetrathia4.4metacyclophanes to the correspondingsyn‐ andanti‐dithia3.3metacyclophanes
机译:Hindered organoboron groups in organic synthesis. 17 1. Synthesis of 2,4,6‐triisopropylphenylborane (TripBH2)2, a useful alternative to thexylborane
机译:1,2,3‐Selenadiazoles as precursors to cyclopentadienylcobalt dithiolenes and 1,4‐dithiins: molecular structures of bis(cycloocteno)‐1,4‐dithiin and bis(cycloocteno)‐1,4‐diselenin
机译:Stereospecific synthesis ofP‐epimeric (Rp1,Rp2)‐bis‐O‐l‐menthylphenylphosphonothionyl diselenide. A new variant of the stereoselective Staudinger reaction