G. Penn

发表

Synthesis of a Precursor to Sacubitril Using Enabling Technologies.

S. Ley, B. Martin, Samuel L. Bourne, 2015, Organic letters.

Enzymatic resolution of endo-bicyclo[2.2.1]hept-2-yl butybates and related compounds: steric requirements in the bridge-region

K. Faber, Christoph Marschner, H. Griengl, 1989 .

Enzymatic preparation of optically active 7-oxabicyclo[2.2.1] heptane derivatives

K. Faber, R. Saf, H. Griengl, 1988 .

Enzymatic resolution of norbornane-type esters

K. Faber, H. Griengl, G. Penn, 1987 .

Reactions of cyclic oxalyl compounds, 37. Substituent effects on the site of nucleophilic attack at 1H‐pyrrole‐2,3‐diones

C. Kappe, K. Peters, E. Terpetschnig, 1995 .

Synthesis of α- and β- D,L-ribo-carbahex-2-ulofuranose

Christoph Marschner, H. Griengl, G. Penn, 1993 .

Synthesis of α- and β-D-carbaribofuranose from (+)-norborn-5-en-2-one

Christoph Marschner, H. Griengl, G. Penn, 1990 .

Reactions of cyclic oxalyl compounds — 38. New isoindigoide dyes from heterocyclic 2,3-diones — Synthesis and thermal rearrangement☆

K. Peters, W. Fabian, E. Peters, 1996 .

Reactions of cyclic oxalyl compounds - 32.

K. Peters, E. Terpetschnig, E. Peters, 1991 .

Heterogeneous vs. homogeneous catalysis in manufacturing of terbinafine a case study for route selection of an industrial process

Christian Fleury, B. Schenkel, U. Beutler, 1997 .

Phosphonoformate and phosphonoacetate derivatives of 5-substituted 2'-deoxyuridines: synthesis and antiviral activity.

E. De Clercq, B. Rosenwirth, H. Griengl, 1988, Journal of medicinal chemistry.

New synthesis of oxcarbazepine via remote metalation of protected N-o-tolyl-anthranilamide derivatives

P. Furet, U. Beutler, W. Zaugg, 2001 .

Heteroanalogous deazapurines via novel 4 + 2 cycloaddition reactions of ketenimines

K. Peters, E. Peters, H. Schnering, 1987 .

Oxoketene-oxoketene, imidoylketene-imidoylketene and oxoketenimine-imidoylketene rearrangements. 1,3-Shifts of phenyl groups.

C. Wentrup, G. Kollenz, G. Penn, 2006, Organic & biomolecular chemistry.

Large scale preparation of (+)- and (−)-endo-norbornenol by enzymatic hydrolysis

K. Faber, H. Griengl, G. Penn, 1986 .