Louis M. Leichter

New synthetic reactions. Geminal alkylation via .alpha.-trimethylenedithiocyclobutanones

Synthesis and thermal rearrangement of tricyclo[3.2.02,4]hept-6-enes. Analysis of structural requirements for effective intramolecular trapping of a 1,3-diradical by a remote cyclobutene ring

Unsaturated heterocyclic systems. LV. Cycloaddition reactions of derivatives of 1H-azepine

Tricyclo[4.1.0.02,5]hept-3-ene to quadricyclane rearrangement. Intramolecular trapping of a 1,3-diradical by a remote cyclobutene ring

Pyrolysis of anti-tricyclo[3.2.0.02,4]heptanes. Role of 2,4 substitution in the operation of .sigma. bond assisted cyclobutane fragmentations

Silver(I) ion-catalyzed rearrangements of strained .sigma. bonds. IX. Regio- and stereoselective methyl migrations in silver(I)-promoted rearrangements of tricyclo[3.2.0.02,4]heptanes

Thermally promoted cleavage reactions of anti-tricyclo[3.2.0.02,4] heptanes. Influence of 2,4 substitution on competitive bond scission processes

NEW SYNTHETIC REACTIONS, GEMINAL ALKYLATION VIA ALPHA-TRIMETHYLENEDITHIOCYCLOBUTANONES

DURCH AG(I)-IONEN KATALYSIERTE UMLAGERUNGEN GESPANNTER SIGMA-BINDUNGEN 9. MITT. REGIO- UND STEREOSELEKTIVE METHYLWANDERUNGEN BEI AG(I)-PROMOTIERTEN UMLAGERUNGEN VON TRICYCLO(3,2,0,0(2,4))HEPTANEN

PYROLYSE VON ANTI-TRICYCLO(3,2,0,0(2,4))HEPTANEN, BEDEUTUNG DER 2,4-SUBSTITUTION FUER DIE DURCH SIGMA-BINDUNGEN BESCHLEUNIGTEN FRAGMENTIERUNGEN VON CYCLOBUTAN