2004

Zhu, M.; Ruijter, E.; Wessjohann, L.A. “A new scavenger resin for the reversible linking and monoprotection of functionalized aromatic aldehydes.Org Lett. 2004, 6, 3921-3924.

Org Lett Ruijter

Scheid, G.; Ruijter, E.; Konarzycka-Bessler, M.; Bornscheuer, U.T.; Wessjohann, L.A. “Synthesis and resolution of a key building block for epothilones: a comparison of asymmetric synthesis, chemical and enzymatic resolution.Tetrahedron: Asymm. 2004, 15, 2861-2869.

Tet Asym Ruijter

Scheid, G.; Kuit, W.; Ruijter, E.; Orru, R.V.A.; Henke, E.; Bornscheuer, U.; Wessjohann, L.A. “A New Route to Protected Acyloins and Their Enzymatic Resolution with Lipases.Eur. J. Org. Chem. 2004, 1063-1074.

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2003

Vugts, D.J.; Jansen, H.; Schmitz, R.F.; de Kanter, F.J.J.; Orru, R.V.A. “A novel four-component reaction for the synthesis of functionalised dihydropyrimidines” Chem. Comm. 2003, 20, 2594-2595.

Chem Comm Vugts

Bon, R.S.; Hong, C.G.; Bouma, M.J.; Schmitz, R.F.; de Kanter, F.J.J.; Lutz, M.; Spek, A.L.; Orru, R.V.A. “Novel multicomponent reaction for the combinatorial synthesis of 2-imidazolines” Org. Lett. 2003, 5, 3759-3762.

Org Lett Bon

Orru, R.V.A.; de Greef, M. “Recent advances in solution-phase multicomponent methodology for the synthesis of heterocyclic compounds” Synthesis Stuttgart 2003, 10, 1471-1499.

Orru, R.V.A.; Groenendaal, B.; van Heyst, J.; Hunting, M.; Wesseling, C.; Schmitz, R.F.; Mayer, S.F.; Faber, K. “Biomimetic approach to the stereoselective synthesis of acetogenins” Pure Appl. Chem. 2003, 75, 259-264.

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2002

Mayer, S.F.; Steinreiber, A.; Orru, R.V.A.; Faber, K. “Chemoenzymatic asymmetric total syntheses of antitumor agents (3R,9R,10R)- and (3S,9R,10R)-panaxytriol and (R)- and (S)-falcarinol from Panax ginseng using an enantioconvergent enzyme-triggered cascade reaction” J. Org. Chem. 2002, 67, 9115-9121.

JOC Mayer

Schrekker, H.S.; de Bolster, M.W.G.; Orru, R.V.A.; Wessjohann, L.A. “In situ formation of allyl ketones via Hiyama-Nozaki reactions followed by a chromium-mediated Oppenauer oxidation” J. Org. Chem. 2002, 67, 1975-1981.

JOC Schrekker

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2001

Mayer, S.F.; Steinreiber, A.; Orru, R.V.A.; Faber, K. “Enzyme-triggered enantioconvergent transformation of haloalkyl epoxides” Eur. J. Org. Chem. 2001, 23, 4537-4542.

Mayer, S.F.; Steinreiber, A.; Orru, R.V.A.; Faber, K. “An enzyme-triggered enantio-convergent cascade-reaction” Tetrahedron: Asymmetry 2001, 12, 41-43.

Steinreiber, A.; Hellstrom, H.; Mayer, S.F.; Orru, R.V.A.; Faber, K. “Chemo-enzymatic enantioconvergent synthesis of C-4-building blocks containing a fully substituted chiral carbon center using bacterial epoxide hydrolases” Synlett 2001, 1, 111-113.

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2000

Steinreiber, A.; Osprian, I.; Mayer, S.F.; Orru, R.V.A.; Faber, K. “Enantioselective hydrolysis of functionalized 2,2-disubstituted oxiranes with bacterial epoxide hydrolases” Eur. J. Org. Chem. 2000, 22, 3703-3711.

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1999

van der Werf, M.J.; Orru, R.V.A.; Overkamp, K.M.; Swarts, H.J.; Osprian, I.; Steinreiber, A.; de Bont, J.A.M.; Faber, K. “Substrate specificity and stereospecificity of limonene-1,2-epoxide hydrolase from Rhodococcus erythropolis DCL14; an enzyme showing sequential and enantioconvergent substrate conversion” Appl. Microbiol. Biotechnol. 1999, 52, 380-385.

Osprian, I.; Jarret, C.; Strauss, U.; Kroutil, W.; Orru, R.V.A.; Felfer, U.; Willetts, A.J.; Faber, K. “Large-scale preparation of a nitrile-hydrolysing biocatalyst: Rhodococcus R 312 (CBS 717.73)” J. Mol. Catal. B: Enzym. 1999, 6, 555-560.

Orru, R.V.A.; Faber, K. “Stereoselectivities of microbial epoxide hydrolases” Curr. Opin. Chem. Biol. 1999, 3, 16-21.

Orru, R.V.A.; Archelas, A.; Furstoss, R.; Faber, K. “Epoxide hydrolases and their synthetic applications” Adv. Biochem. Eng./Biotechnol. 1999, 63, 145-167.

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1998

Orru, R.V.A.; Osprian, I.; Kroutil, W.; Faber, K. “An efficient large-scale synthesis of (R)-(-)-mevalonolactone using simple biological and chemical catalysts” Synthesis-Stuttgart 1998, 9, 1259-1263.

Kroutil, W.; Orru, R.V.A.; Faber, K. “Stabilization of Nocardia EH1 epoxide hydrolase by immobilization” Biotechnol. Lett. 1998, 20, 373-377.

Orru, R.V.A.; Mayer, S.F.; Kroutil, W.; Faber, K. “Chemoenzymatic deracemization of (+/-)-2,2-disubstituted oxiranes” Tetrahedron 1998, 54, 859-874.

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1997

Orru, R.V.A.; Kroutil, W.; Faber, K. “Deracemization of (+/-)-2,2-disubstituted epoxides via enantioconvergent chemoenzymatic hydrolysis using Nocardia EH1 epoxide hydrolase and sulfuric acid” Tetrahedron Lett. 1997, 38, 1753-1754.

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1996

Piet, D.P.; Orru, R.V.A.; Jenniskens, L.H.D.; van de Haar, C.; van Beek, T.A.; Franssen, M.C.R.; Wijnberg, J.B.P.A.; de Groot, A. “Synthesis of (1 alpha,7 alpha,8 beta)-(+/-)-8-methyl-2-methylenebicyclo[5.3.0]dec-5-en-8-ol. Structure revision of natural dictamnol” Chem. Pharm. Bull. 1996, 44, 1400-1403.

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1995

Bastiaansen, P.M.F.M.; Orru, R.V.A.; Wijnberg, J.B.P.A.; De Groot, A. “Long-range effects of through-bond orbital interactions on the desilylation rate of silyl ethers” J. Org. Chem. 1995, 60, 6154-6158.

Orru, R.V.A.; Wijnberg, J.B.P.A.; De Groot, A. “Substituent effects on through-bond orbital interaction-induced heterolysis of some perhydronaphtalene-1,4-diol monosulfonate esters” J. Org. Chem. 1995, 60, 4233-4239.

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1994

De Groot, A.; Jansen, B.J.M.; Verstegen Haaksma, A.A.; Swarts, H.J.; Orru, R.V.A.; Stork, G.A.; Wijnberg, J.B.P.A. “Recent Developments in the synthesis of drimane and lactarane sesquiterpenes” Pure Appl. Chem. 1994, 66, 2053-2056.

Orru, R.V.A.; Wijnberg, J.B.P.A.; Bouwman, C.T.; De Groot, A. “Rearrangement vs homofragmentation – chemical consequences of different sigma-relays on the heterolysis of sulfonate esters induced by through-bond interactions” J. Org. Chem. 1994, 59, 374-382.

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1993

Orru, R.V.A.; Wijnberg, J.B.P.A.; Jennikens, L.H.D.; De Groot, A. “Intramolecular alkoxide induced heterolysis of perhydronaphtalene-1,4-diol monosulfonate esters through orbital interactions over 3 C-C single bonds” J. Org. Chem. 1993, 58, 1199-1206.

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1990

Gijsen, H.J.M.; Kanai, K.; Stork, G.A.; Wijnberg, J.B.P.A.; Orru, R.V.A.; Seelen, C.G.J.M.; van der Kerk, S.M.; De Groot, A. “The conversion of natural (+)-aromadendrene into chiral synthons.1.” Tetrahedron 1990, 46, 7236-7246.