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Synthesis of Aristotelia-Type Alkaloids, Part XVI.
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- Helvetica Chimica Acta, 2002, v. 85, n. 10, p. 3400, doi. 10.1002/1522-2675(200210)85:10<3400::AID-HLCA3400>3.0.CO;2-2
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Synthesis and Conformational Analysis of All Eight Diastereoisomers of 5-Methylyohimbane.
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- Helvetica Chimica Acta, 2002, v. 85, n. 3, p. 945, doi. 10.1002/1522-2675(200203)85:3<945::AID-HLCA945>3.0.CO;2-A
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Some Observations Concerning the Thermally Induced Oxy-Ene Reaction.
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- Helvetica Chimica Acta, 2001, v. 84, n. 2, p. 388, doi. 10.1002/1522-2675(20010228)84:2<388::AID-HLCA388>3.0.CO;2-P
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The First Examples of Successful Anionic Oxy-Ene Reactions.
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- Helvetica Chimica Acta, 2001, v. 84, n. 2, p. 401, doi. 10.1002/1522-2675(20010228)84:2<401::AID-HLCA401>3.0.CO;2-7
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Towards a New Synthetic Entry into the Iboga-Alkaloid Family.
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- Helvetica Chimica Acta, 2000, v. 83, n. 8, p. 1753, doi. 10.1002/1522-2675(20000809)83:8<1753::AID-HLCA1753>3.0.CO;2-G
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A Reinvestigation of the Oxidative Rearrangement of Yohimbane-Type Alkaloids. Part B. Formation of Oxindol (= 1,3-Dihydro-2 H-indol-2-one) Derivatives.
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- Helvetica Chimica Acta, 1996, v. 79, n. 5, p. 1361, doi. 10.1002/hlca.19960790510
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Total Synthesis of (+)-Elacomine and (−)-Isoelacomine, Two Hitherto Unnamed Oxindole Alkaloids from Elaeagnus commutata.
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- Helvetica Chimica Acta, 1996, v. 79, n. 1, p. 151, doi. 10.1002/hlca.19960790116
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Synthesis of the Dolabellane Diterpene Hydrocarbon (±)-δ-araneosene.
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- Helvetica Chimica Acta, 1995, v. 78, n. 3, p. 715, doi. 10.1002/hlca.19950780318
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Synthesis of Aristotelia-Type Alkaloids. Part XV. Total synthesis of (+)-hobartinol.
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- Helvetica Chimica Acta, 1995, v. 78, n. 2, p. 292, doi. 10.1002/hlca.19950780204
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Synthesis of Aristotelia-Type Alkaloids. Part XIII. Total syntheses of (+)-makonine, (+)-aristotelinone, and (+)-11,12-didehydroaristoteline.
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- Helvetica Chimica Acta, 1994, v. 77, n. 8, p. 2125, doi. 10.1002/hlca.19940770805
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A Reinvestigation of the Oxidative Rearrangement of Yohimbane-Type Alkaloids. Part A. Formation of pseudoindoxyl ( = 1,2-dihydro-3 H-indol-3-one) derivatives.
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- Helvetica Chimica Acta, 1994, v. 77, n. 5, p. 1331, doi. 10.1002/hlca.19940770514
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Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3 H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2 H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3 H-indol-3-ones)
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- Helvetica Chimica Acta, 1993, v. 76, n. 5, p. 1847, doi. 10.1002/hlca.19930760505
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Investigations Concerning an Unexpected Reaction between the Dimsyl Anion ( = (Methylsulfinyl)methanide) and a γ,δ-Epoxy-ketone.
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- Helvetica Chimica Acta, 1992, v. 75, n. 1, p. 190, doi. 10.1002/hlca.19920750117
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Synthesis of Aristotelia-type alkaloids. Part IX. Synthesis of (±)-alloaristoteline.
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- Helvetica Chimica Acta, 1991, v. 74, n. 8, p. 1643, doi. 10.1002/hlca.19910740805
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Synthesis of Aristotelia-Type Alkaloids. Part VIBiomimetic Synthesis of (+)-Aristofruticosine.
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- Helvetica Chimica Acta, 1991, v. 74, n. 1, p. 110, doi. 10.1002/hlca.19910740113
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Synthesis of Aristotelia-type alkaloids. Part VII. Syntheses of (±)-sorelline, (±)-serratenone, and (±)-aristotelin-19-one.
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- Helvetica Chimica Acta, 1991, v. 74, n. 2, p. 275, doi. 10.1002/hlca.19910740204
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Synthesis of Aristotelia-Type Alkaloids.. Part IV. Synthesis of (±)-aristoserratine.
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- Helvetica Chimica Acta, 1989, v. 72, n. 2, p. 254, doi. 10.1002/hlca.19890720209
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Synthesis of Aristotelia-Type Alkaloids. Part III. (3 R,4 R)- and (3 R,4 S)-1- p-menthene-3,8-diol and the corresponding racemates: Preparation and assignment of configuration.
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- Helvetica Chimica Acta, 1988, v. 71, n. 1, p. 209, doi. 10.1002/hlca.19880710122
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Synthesis of aristoteline-type alkaloids. Part II. The structure of neohobartine, a side product of the hobartine-aristoteline transformation.
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- Helvetica Chimica Acta, 1984, v. 67, n. 7, p. 1878, doi. 10.1002/hlca.19840670725
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Synthesis of (−)-Hobartine and Related Indole Alkaloids.
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- Helvetica Chimica Acta, 1984, v. 67, n. 4, p. 1040, doi. 10.1002/hlca.19840670417
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Construction of Large Carbocyclic Rings by Ireland-Claisen Rearrangement of O-Silylated Lactone Enolates: Synthesis of (±)-muscone.
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- Helvetica Chimica Acta, 1983, v. 66, n. 8, p. 2608, doi. 10.1002/hlca.19830660827
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Preparation of [<sup>13</sup>C<sub>2</sub>]DMS.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1991, v. 29, n. 8, p. 957, doi. 10.1002/jlcr.2580290813
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