Jordi Bach

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A synthetic approach towards octalactin A, based on the stereoselective reduction of α,β-unsaturated ketones

J. Vilarrasa, Jordi García, Jordi Bach, 1995 .

A Synthetic Approach to 3-Hydroxy 4-Substituted Carboxylic Acids based on the Stereoselective Reduction of 1-Trimethylsilyl-1-alkyn-3-ones

Jordi García, Marta López, Jordi Bach, 2000 .

Oxazaborolidine-catalysed reduction of alk-2-ene-1,4-diones. A convenient access to chiral 1,4-diols

J. Vilarrasa, Jordi García, Marta López, 1998 .

Highly Enantioenriched Propargylic Alcohols by Oxazaborolidine-Mediated Reduction of Acetylenic Ketones.

J. Vilarrasa, Jordi García, Jordi Bach, 1996, The Journal of organic chemistry.

Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1.

A. P. Hodgson, R. Oballa, K. Gibson, 2001, Angewandte Chemie.

Allylic alcohols of unexpected configuration by oxazaborolidine-catalysed reduction of α,β-unsaturated ketones. An explanation based on MO calculations

J. Vilarrasa, J. Farrás, Jordi García, 1995 .

Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1.

A. P. Hodgson, R. Oballa, K. Gibson, 2001, Angewandte Chemie.

Stereoselective reduction of unsaturated 1,4-diketones. A practical route to chiral 1,4-diols

J. Vilarrasa, Jordi García, Jordi Bach, 1997 .

Syntheses of the C-1 alkyl side chains of Zaragozic acids A and C

J. Vilarrasa, P. Romea, F. Urpí, 1998 .

Stereoselective reduction of α′-branched α,β-ynones. Application to the synthesis of the Octalactin A ring

Jordi García, Jordi Bach, 1998 .

Highly Enantioenriched Propargylic Alcohols by Oxazaborolidine‐ Mediated Reduction of Acetylenic Ketones.

J. Vilarrasa, Jordi García, Jordi Bach, 1997 .

Allylic Alcohols of Unexpected Configuration by Oxazaborolidine- Catalyzed Reduction of α,β-Unsaturated Ketones. An Explanation Based on MO Calculations.

J. Vilarrasa, J. Farrás, Jordi Bach, 2010 .

N-acyl-5,5-dimethyloxazolidin-2-ones as latent aldehyde equivalents.

S. Davies, Andrew D. Smith, S. Bull, 2003, Organic & biomolecular chemistry.

N-ACYL-5,5-DIMETHYL-OXAZOLIDIN-2-ONES AS LATENT ALDEHYDE EQUIVALENTS

S. Davies, Andrew D. Smith, S. Bull, 1999 .

Efficient three-step sequence for the deamination of α-aminoesters. Application to the synthesis of CysLT1 antagonists

H. Ryder, J. Sanahuja, L. Sole, 2009 .

The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment.

I. Paterson, M. J. Coster, J. L. Aceña, 2005, Organic & biomolecular chemistry.

The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation.

I. Paterson, M. J. Coster, J. L. Aceña, 2005, Organic & biomolecular chemistry.

Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncation.

I. Paterson, M. J. Coster, J. L. Aceña, 2003, Chemical communications.

A Synthetic Approach Towards Octalactin A, Based on the Stereoselective Reduction of α,β-Unsaturated Ketones.

J. Vilarrasa, Jordi García, Jordi Bach, 1995 .

Highly stereoselective approach to alk-2-yne-1,4-diols by oxazaborolidine-mediated reduction of alk-2-yne-1,4-diones.

M. Fontes, J. Farrás, X. Ariza, 2004, The Journal of organic chemistry.

Fast and Efficient Access to a Family of Multifunctional 1,3,5-Trisubstituted Piperidines

J. Díaz, R. Lavilla, D. Fernández-Forner, 2008 .