Hans‐Jürg Borschberg

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A highly stereoselective in vitro cyclization of dolabellatriene diterpenes into novel dolastadienes

P. Acklin, L. Jenny, Hans‐Jürg Borschberg, 1996 .

Total Synthesis of (+)‐Elacomine and (−)‐Isoelacomine, Two Hitherto Unnamed Oxindole Alkaloids from Elaeagnus commutata

C. Pellegrini, Hans‐Jürg Borschberg, Michael A. Weber, 1996 .

The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part I. General strategy and search for a convenient diene for the construction of a key tricyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part II. Model studies for rings B and C of (+)-anhydroryanodol. Preparation of a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol

A. Bélanger, C. Liao, J. Maffrand, 1990 .

Total synthesis of ryanodol

A. Bélanger, C. Liao, J. Maffrand, 1979 .

Synthesis of aristoteline‐type alkaloids. Part II. The structure of neohobartine, a side product of the hobartine‐aristoteline transformation

Hans‐Jürg Borschberg, 1984 .

Synthesis of (−)‐Hobartine and Related Indole Alkaloids

T. Darbre, Hans‐Jürg Borschberg, Cornelius Nossbaumer, 1984 .

Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3H-indol-3-ones)†

R. Güller, Hans‐Jürg Borschberg, 1993 .

A stereoselective transformation of pseudoindoxyls into oxindoles in a single operation

R. Güller, Hans‐Jürg Borschberg, 1994 .

Synthesis of the oxindole alkaloid (−)-horsfiline

C. Pellegrini, C. Strässler, Hans‐Jürg Borschberg, 1994 .

Synthesis of Aristotelia-type alkaloids. Part VIII. Synthesis of (±)-aristolasicone†

M. Dobler, R. Güller, Hans‐Jürg Borschberg, 1991 .

Synthesis of aristotelia-type alkaloids. Part X. Biomimetic transformation of synthetic (+)-aristoteline into (−)-alloaristoteline.

R. Güller, Hans‐Jürg Borschberg, 1992 .

New Strategies for the Synthesis of Monoterpene Indole Alkaloids

Hans‐Jürg Borschberg, 2005 .

Synthesis of Aristotelia-Type Alkaloids.. Part IV. Synthesis of (±)-aristoserratine†‡

Hans‐Jürg Borschberg, S. Burkard, 1989 .

Investigations Concerning an Unexpected Reaction between the Dimsyl Anion ( = (Methylsulfinyl)methanide) and a γ,δ-Epoxy-ketone

Hans‐Jürg Borschberg, R. Beerli, 1992 .

Construction of large carbocyclic rings by Ireland-Claisen rearrangement of O-silylated lactone enolates: synthesis of (±)-muscone

R. Brunner, Hans‐Jürg Borschberg, 1983 .

Synthesis of Aristotelia-Type Alkaloids. Part III. (3R,4R)- and (3R,4S)-1-p-menthene-3,8-diol and the corresponding racemates: Preparation and assignment of configuration†

Hans‐Jürg Borschberg, S. Burkard, M. Looser, 1988 .

Chapter 3 - Aristotelia Alkaloids

Hans‐Jürg Borschberg, 1996 .

Synthesis of Aristotelia‐Type Alkaloids. Part XV. Total synthesis of (+)‐hobartinol

M. Dobler, James C. Anderson, M. Juch, 1995 .

Chirality transfer in an Ireland–Claisen rearrangement: a new approach toward the Iboga alkaloids

Florian M. Koch, Stefan Höck, Hans‐Jürg Borschberg, 2004 .

Preparation of [13C2]DMS

Hans‐Jürg Borschberg, R. Beerli, 1991 .

Stereoelectronic control in the reductive opening of cyclopropylogous α-haloketones

Hans‐Jürg Borschberg, R. Beerli, E. Brunner, 1992 .

Synthesis of the Dolabellane Diterpene Hydrocarbon (±)‐δ‐araneosene

L. Jenny, Hans‐Jürg Borschberg, 1995 .

Microbial hydroxylation of some synthetic Aristotelia alkaloids

M. Dobler, R. Azerad, Hans‐Jürg Borschberg, 1995 .

Synthesis of Aristotelia-type alkaloids. Part XIV. Total synthesis of (+)-aristolone

M. Dobler, Hans‐Jürg Borschberg, 1994 .

Synthesis of Aristotelia-type alkaloids. Part XI. Total syntheses of (+)-sorelline and (+)-aristolasene

M. Dobler, Hans‐Jürg Borschberg, R. Beerli, 1992 .

Synthesis of Aristotelia-type alkaloids. Part VII. Syntheses of (±)-sorelline, (±)-serratenone, and (±)-aristotelin-19-one†

Hans‐Jürg Borschberg, S. Burkard, 1991 .

Synthesis of Aristotelia‐Type Alkaloids. Part VIBiomimetic Synthesis of (+)‐Aristofruticosine

Hans‐Jürg Borschberg, R. Beerli, 1991 .

Synthesis of Aristotelia-Type Alkaloids. Part XIII. Total syntheses of (+)-makonine, (+)-aristotelinone, and (+)-11,12-didehydroaristoteline†

R. Güller, Hans‐Jürg Borschberg, R. Stahl, 1994 .

A Reinvestigation of the Oxidative Rearrangement of Yohimbane‐Type Alkaloids. Part B. Formation of Oxindol (= 1,3‐Dihydro‐2H‐indol‐2‐one) Derivatives

Hans‐Jürg Borschberg, R. Stahl, 1994 .

Enantioselective Synthesis of (−)‐(19R)‐Ibogamin‐19‐ol

Stefan Höck, Hans‐Jürg Borschberg, 2006 .

Synthesis of Aristotelia‐type alkaloids. Part IX. Synthesis of (±)‐alloaristoteline

R. Güller, Hans‐Jürg Borschberg, 1991 .

The Total Synthesis of (+)-Ryanodol. Part 1. General Strategy and Search for a Convenient Diene for the Construction of a Key Tricyclic Intermediate.

A. Bélanger, C. Liao, J. Maffrand, 1990 .

Reinvestigation of the Oxidative Rearrangement of Yohimbane-Type Alkaloids. Part A. Formation of Pseudoindoxyl (= 1,2-Dihydro-3H-indol- 3-one) Derivatives.

Hans‐Jürg Borschberg, R. Stahl, 2010 .