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Attributs	Valeurs
type	Person
name	Hudlicky Tomas
familyName	Hudlicky
Given name	Tomas
is relates of	http://hub.abes.fr/acs/periodical/joceah/1980/volume_45/issue_25/101021jo01313a003/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_20/101021jo00168a050/authorship/2 http://hub.abes.fr/acs/periodical/joceah/1994/volume_59/issue_26/101021jo00105a002/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_8/101021jo00347a031/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_26/101021jo00174a031/authorship/3 http://hub.abes.fr/acs/periodical/joceah/1990/volume_55/issue_9/101021jo00296a004/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_20/101021jo00168a010/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_17/101021jo00043a037/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_6/101021jo00032a061/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_8/101021jo00060a061/authorship/2 http://hub.abes.fr/acs/periodical/jacsat/1980/volume_102/issue_20/101021ja00540a036/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1989/volume_111/issue_25/101021ja00207a040/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1994/volume_116/issue_12/101021ja00091a012/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2007/volume_72/issue_13/101021jo070099t/authorship/4 http://hub.abes.fr/acs/periodical/jnprdf/2008/volume_71/issue_3/101021np0705357/authorship/4 http://hub.abes.fr/acs/periodical/jnprdf/2005/volume_68/issue_1/101021np0307688/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_25/101021jo020129m/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_2/101021jo0235930/authorship/1 http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_9/101021jo040292c/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/2002/volume_124/issue_35/101021ja0205378/authorship/6 http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_8/101021jo00321a047/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_19/101021jo00228a049/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_9/101021jo00244a020/authorship/2 http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_9/101021jo00244a047/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1984/volume_49/issue_10/101021jo00184a042/authorship/6 http://hub.abes.fr/acs/periodical/joceah/1986/volume_51/issue_24/101021jo00374a055/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1990/volume_55/issue_15/101021jo00302a056/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_5/101021jo00057a001/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_22/101021jo00222a020/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1990/volume_55/issue_15/101021jo00302a037/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_11/101021jo00011a031/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_21/101021jo00221a043/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_20/101021jo00229a051/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1991/volume_56/issue_15/101021jo00015a006/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_3/101021jo00029a049/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1975/volume_97/issue_2/101021ja00835a026/authorship/2 http://hub.abes.fr/acs/periodical/jacsat/1989/volume_111/issue_17/101021ja00199a032/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_14/101021jo00327a014/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_24/101021jo00172a003/authorship/4 http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_1/101021jo00201a026/authorship/1 http://hub.abes.fr/acs/periodical/joceah/1989/volume_54/issue_17/101021jo00278a052/authorship/1 http://hub.abes.fr/acs/periodical/jnprdf/1987/volume_50/issue_4/101021np50052a012/authorship/9 http://hub.abes.fr/acs/periodical/joceah/1994/volume_59/issue_15/101021jo00094a005/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1978/volume_100/issue_15/101021ja00483a045/authorship/2 http://hub.abes.fr/acs/periodical/chreay/1989/volume_89/issue_7/101021cr00097a004/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1990/volume_112/issue_25/101021ja00181a081/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1992/volume_114/issue_24/101021ja00050a079/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1994/volume_116/issue_12/101021ja00091a011/authorship/1 http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_12/101021ja00117a046/authorship/2 http://hub.abes.fr/acs/periodical/chreay/1989/volume_89/issue_1/101021cr00091a005/authorship/6 http://hub.abes.fr/acs/periodical/joceah/1973/volume_38/issue_6/101021jo00946a043/authorship/3
is Author of	SRN1 mechanism in heteroaromatic nucleophilic substitution. Photostimulation and entrainment of the reaction of lithioacetone with 2-chloroquinoline Intramolecular [4 + 1] pyrroline annulation via azide-diene cycloadditions. 2. Formal stereoselective total syntheses of (.+-.)-platynecine, (.+-.)-hastanecine, (.+-.)-turneforcidine, and (.+-.)-dihydroxyheliotridane Cyclopentene annulation via intramolecular addition of diazoketones to 1,3-dienes. Applications to the synthesis of cyclopentanoid terpenes Menthyl 2-bromocrotonate and menthyl 4-bromocrotonate: reagents for chiral vinylogous Darzens and Reformatsky reactions Chemoenzymic enantiocontrolled synthesis of (-)-specionin Selectivity in [2+3] and [4+3] annulations. Cope rearrangement of (silyloxy)divinylcyclopropane systems leading to functionalized bicyclo[3.2.n]alkenyl derivatives Microbial Oxidation of Aromatics in Enantiocontrolled Synthesis. 3. Design of Amino Cyclitols (exo-Nitrogenous) and Total Synthesis of (+)-Lycoricidine via Acylnitrosyl Cycloaddition to Polarized 1-Halo-1,3-cyclohexadienes Studies in the regioselectivity of the vinylogous Reformatsky reaction with ambident electrophiles: reversibility, mechanism, and synthetic utility Stereocontrolled total synthesis of pentalenenes via [2 + 3] and [4 + 1] cyclopentene annulation methodologies A new [2 + 3] annulation for highly functionalized dihydrofurans via carbon-carbon bond formation Intramolecular Simmons-Smith reaction and other synthetic alternatives to cyclopropanation of dienic diazo ketones. Parallel decomposition pathways of a sterically congested diazo ketone and its vinylcyclopropane under thermal, photolytic, acid-catalyzed, and radical-release conditions Heteroatom cyclopentene annulation. Synthesis of guaiane ring system General Method of Synthesis for Natural Long-Chain β/-Diketones 4-Siloxy-.alpha.-bromocrotonate: a new reagent for [2+3] annulation leading to oxygenated cyclopentenes at low temperatures Yeast-mediated resolution of .beta.-keto esters of prochiral alcohols The [2 + 3] and [3 + 4] annulation of enones. Enantiocontrolled total synthesis of (-)-retigeranic acid [Erratum to document cited in CA111(11):97589v] Enantioselective synthesis of (-)-zeylena from styrene New vinylcyclopropanation methodology and reagents for potential [2 + 3] cyclopentene, dihydrofuran, and pyrroline annulations Rational design of aza sugars via biocatalysis: mannojirimycin and other glycosidase inhibitors The [2 + 3] and [3 + 4] annulation of enones. Enantiocontrolled total synthesis of (-)-retigeranic acid Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: trihydroxyheliotridanes Synthesis of .beta.-methoxy enones via a new two-carbon extension of carboxylic acids Anionic approaches to the construction of cyclopentanoids Studies in Cephalotaxus alkaloids. Stereospecific total synthesis of homoharringtonine Short syntheses of eburnamonine via .beta.-oxycyclopropylcarbonyl and related intermediates Intramolecular cyclopentene annulation. 2. Synthesis and carbon-13 nuclear magnetic resonance spectroscopy of bicyclo[4.3.0]non-7-en-2-ones Use of cyclopropanes and their derivatives in organic synthesis Total synthesis of (.+-.)-hirsutene Reactions of Indole Derivatives with Oxiranes and Aziridines onSilica. Synthesis of β-Carbolin-1-one Mimic of Pancratistatin Synthesis, Structure, and Biological Evaluation of Novel N-and O-Linked Diinositols Biocatalysis. Fundamentals and Applications By A. S.Bommarius (Georgia Institute of Technology) and B. R. Riebel(Emory University). Wiley-VCH, Weinheim, Germany. 2004.xxiii + 611 pp. 7 × 10 1/2 in. $175.00. ISBN 3-527-30344-8. Total Synthesis andBiological Evaluation of Amaryllidaceae Alkaloids: Narciclasine,ent-7-Deoxypancratistatin, Regioisomer of 7-Deoxypancratistatin,10b-epi-Deoxypancratistatin, and Truncated Derivatives. Total Synthesis and Biological Evaluation of AmaryllidaceaeAlkaloids: Narciclasine, ent-7-Deoxypancratistatin, Regioisomer of7-Deoxypancratistatin, 10b-epi-Deoxypancratistatin, andTruncated Derivatives1 Unexpected Reactivity of the Burgess Reagentwith Thiols: Synthesis of Symmetrical Disulfides Chiral Version of the Burgess Reagent and Its Reactions with Oxiranes: Application to the Formal Enantiodivergent Synthesis of Balanol A short synthesis of (+)-lycoricidine Two topologically distinct total syntheses of (.+-.)-sarkomycin General method of synthesis of cyclopentanoid terpenic acids. Stereocontrolled total syntheses of (.+-.)-isocomenic acid and (.+-.)-epiisocomenic acid Oxa- and Azabicyclo[4.1.0]heptenes as New Synthons for C-Disaccharide and Alkaloid Synthesis. Reactivity Trends with Carbon Nucleophiles Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol Microbial Oxidation of Aromatics in Enantiocontrolled Synthesis. 2. Rational Design of Aza Sugars (endo-Nitrogenous). Total Synthesis of (+)-Kifunensine, Mannojirimycin, and Other Glycosidase Inhibitors First Total Synthesis of (+)-Pancratistatin: An Unusual Set of Problems Regioselectivity in the Reformatskii reaction of 4-bromocrotonate. Role of the catalyst and the solvent in the normal vs. abnormal modes of addition to carbonyl substrates Chemoenzymic Synthesis of D-erythro- and L-threo-C18-Sphingosines Unusual oxidation of 1-halo-1,3-dienes with parmanganate. Expedient syntheses of (+)-D-chiro-3-inosose and (+)-D-chiro-inositol from chlorobenzene

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