IUBO institute
Research institute


Massachusetts Institute of Technology
Cambridge, Estados UnidosPublications in collaboration with researchers from Massachusetts Institute of Technology (12)
2021
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Components of a Neanderthal gut microbiome recovered from fecal sediments from El Salt
Communications Biology, Vol. 4, Núm. 1
2014
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Crossover experiments applied to network formation reactions: Improved strategies for counting elastically inactive molecular defects in PEG gels and hyperbranched polymers
Journal of the American Chemical Society, Vol. 136, Núm. 26, pp. 9464-9470
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Photo-Responsive Hydrogels for Adaptive Membranes
Smart Membranes and Sensors: Synthesis, Characterization, and Applications (Wiley Blackwell), pp. 21-51
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The Neanderthal meal: A new perspective using faecal biomarkers
PLoS ONE, Vol. 9, Núm. 6
2008
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HIV-1 protease inhibitors from inverse design in the substrate envelope exhibit subnanomolar binding to drug-resistant variants
Journal of the American Chemical Society, Vol. 130, Núm. 19, pp. 6099-6113
2007
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Design of mutation-resistant HIV protease inhibitors with the substrate envelope hypothesis
Chemical Biology and Drug Design, Vol. 69, Núm. 5, pp. 298-313
1983
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Stereo and reg ioselective openings of chiral 2,3-epoxy alcohols. versatile routes to optically pure natural products and drugs. unusual kinetic resolutions
Pure and Applied Chemistry, Vol. 55, Núm. 4, pp. 589-604
1982
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General Method for Determining Absolute Configurations of Acyclic Allylic Alcohols
Journal of the American Chemical Society, Vol. 104, Núm. 13, pp. 3775-3776
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Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 1. Simple Alditols
Journal of Organic Chemistry
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Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 2. Simple Deoxyalditols
Journal of Organic Chemistry
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Synthesis of Saccharides and Related Polyhydroxylated Natural Products. 3. Efficient Conversion of 2,3-erythro-Aldoses to 2,3-threo-Aldoses
Journal of the American Chemical Society, Vol. 104, Núm. 12, pp. 3515-3516
1981
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Kinetic Resolution of Racemic Allylic Alcohols by Enantioselective Epoxidation. A Route to Substances of Absolute Enantiomeric Purity
Journal of the American Chemical Society, Vol. 103, Núm. 20, pp. 6237-6240