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	1	Substituent Effects on the C‐C Bond Strength, 15 (1) Geminal Substituent Effects, 7 (2). Thermochemistry and Thermal Decomposition of Alkyl‐substituted Tricyanomethyl Compounds Enthalten in Chemische Berichte - recueil Bd. 127, 2007, Nr. 11: 2225-2234. 10 S.
	2	Bimolecular Formation of Radicals by Hydrogen Transfer, 13. † Uncatalyzed Transfer Hydrogenation of Azulene and the Initiation of the Azulene‐Naphthalene Rearrangement Enthalten in Liebigs Annalen - recueil Bd. 1997, 2006, Nr. 10: 2055-2063. 9 S.
	3	Geminal Substituent Effects, 15. † Enthalpies of Formation of a Series of Fluorinated Hydrocarbons and Strain‐Free Group Increments to Assess Polar and Anomeric Stabilization and Strain ‡ Enthalten in Liebigs Annalen - recueil Bd. 1997, 2006, Nr. 7: 1333-1344. 12 S.
	4	Bimolecular Formation of Radicals by Hydrogen Transfer, 12 †. – Transfer hydrogenation of p ‐Substituted α‐Methylstyrenes and of 9‐Methylenefluorene as a Criterion of Mechanism ‡ Enthalten in Liebigs Annalen - recueil Bd. 1997, 2006, Nr. 2: 385-389. 5 S.
	5	Substituent Effects on the C C Bond Strength, 20. – Geminal Substituent Effects, 14. – Stabilization of the Cyano (dimethylamino) methyl Radical – Synergistic effect Due to Interaction Between α‐Amino and α‐Cyano Groups on the Radical Stabilization Energy † Enthalten in Liebigs Annalen - recueil Bd. 1997, 2006, Nr. 1: 155-163. 9 S.
	6	Geminal substituent effects, 11. The anomeric effect in orthoesters — the concept of geminal pairwise interactions for the interpretation of standard enthalpies of formation † Enthalten in Liebigs Annalen - recueil Bd. 1995, 2006, Nr. 12: 2059-2067. 9 S.
	7	Substituent effects on the C C bond strength, 19 †. Geminal substituent effects, 10 ‡. Radical stabilization enthalpies of α,α‐bis (methoxycarbonyl) alkyl and tris (methoxycarbonyl) methyl radicals § Enthalten in Liebigs Annalen - recueil Bd. 1995, 2006, Nr. 8: 1483-1493. 11 S.
	8	Bimolecular formation of radicals by hydrogen transfer, 9 †. Uncatalyzed transfer hydrogenation of α‐methylstyrene by 9,10‐dihydroacridine and N ‐methyl‐9,10‐dihydroacridine ‡ Enthalten in Liebigs Annalen - recueil Bd. 1995, 2006, Nr. 7: 1339-1341. 3 S.
	9	Substituent effects on the CC bond strength, 18 †. Stabilization of alkyl radicals by 4‐pyridyl, 1‐naphthyl or 2‐naphthyl substituents in α‐position ‡ Enthalten in Liebigs Annalen - recueil Bd. 1995, 2006, Nr. 5: 881-884. 4 S.
	10	Substituent effects on the CC bond strength, 17 †. Formation and stability of α‐carbamoylbenzyl radicals Enthalten in Liebigs Annalen - recueil Bd. 1995, 2006, Nr. 5: 877-880. 4 S.

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