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1. Synthesis of enantiopure 3-quinuclidinone analogues with three stereogenic centers: (1S,2R,4S)- and (1S,2S,4S)-2-(hydroxymethyl)-1-azabicyclo[2.2.2]octan-5-one and stereocontrol of nucleophilic addition to the carbonyl group

6. Chelation-controlled reduction of alpha-methylated 8-oxabicyclo[3.2.1]oct-6-en-3-ones with samarium diiodide. Diastereoselective preparation of secondary alcohols

10. Stereoselective synthesis of precursors of naturally occuring robustadials A and

11. Crystal structures of ethanol hemisolvates of (1S,3R,4S,8S,9R)-1N-boranyl-6'-methoxy-cinchonan-9-ol,C20H27BN2O2 center dot 1/2C(2)H(5)OH, and (1S,3S,4S,8S,9R)-1N-boranyl-10,11-didehydro-6 '-methoxy-cinchonan-9-ol, C20H25BN2O2 center dot 1/2C(2)H(5)OH

41. Synthesis of dioxatricyclic segments of dictyoxetane. Oxygenated 6,8-dimethyl-2,7-dioxatricyclo[4.2.1.0 3,8]nonanes show antitumor activity

42. The crystal and molecular structure and solid state conformation of 2,2,4,4,6,6,-hexamethylcyclohexanetrione

43. Nucleophilic Organosilicon Intermediates Turned Electrophilic: (Trimethylsilyl)methyl, Trimethylsilyloxy and also 2-Tetrahydropyranyloxy as Terminators of Cycloadditions of Allyl Cations. A Short Route to Dehydrozizaenes (6-Methylenetricyclo[6.2.1.01,5]-undec-9,10-enes) and Related Tricycles and [3.2.1]-Bicycles.

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