Lucjan Strekowski

Stereoelectronic control in the photorearrangement of .alpha.-chloro ketones. Mechanistic studies in photochemistry. XIII

Stereoelectronic control in the photorearrangement of .alpha.-chloro ketones. Mechanistic studies in organic photochemistry

ELECTRON IMPACT IONIZATION MASS SPECTROMETRY OF DIMETHYLAMINO-, METHOXY-, AND METHYLTHIOPYRIMIDINES. REARRANGEMENTS IN THE MOLECULAR IONS

SYNTHESES WITH PYRIMIDINE-LITHIUM COMPOUNDS. IV. FURTHER STUDY ON THE FORMATION OF BIPYRIMIDINES FROM 5-BROMOPYRIMIDINES

SYNTHESES WITH PYRIMIDINE-LITHIUM COMPOUNDS. III. BIPYRIMIDINES FROM 2,4-DISUBSTITUTED 5-BROMOPYRIMIDINES

SYNTHESES WITH PYRIMIDINE-LITHIUM COMPOUNDS. II. 2,6-BIS(METHYLTHIO)-4,5-DIDEHYDROPYRIMIDINE AS AN INTERMEDIATE IN THE SYNTHESIS OF BIPYRIMIDINES

SYNTHESIS OF 2,4-DISUBSTITUTED 5-BROMOPYRIMIDINES

SYNTHESES WITH PYRIMIDINE-LITHIUM COMPOUNDS PART 1, SYNTHESIS OF SEVERAL 4,5′-BIPYRIMIDINE DERIVATIVES

MECHANISTIC STUDIES IN ORGANIC PHOTOCHEMISTRY PART 11, STEREOELECTRONIC CONTROL IN THE PHOTOREARRANGEMENT OF ALPHA-CHLORO KETONES

ALKYLATION OF 5-ALKYLURACILS WITH 2-DIMETHYLAMINOMETHYL-6-METHYLPHENOL