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Organic layer < Organic layers < Organic ligands  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 16.
Ident.Authors (with country if any)Title
000033 (2012) Patricia García-Domínguez ; Rosana Alvarez [Espagne] ; Ángel R. De Lera [Espagne]Survey of Synthetic Approaches to Natural (Peyssonenynes) and Unnatural Acetoxyenediynes
000070 (2011) Vincent Diemer [France] ; Manon Begaud [France] ; Frédéric R. Leroux [France] ; Françoise Colobert [France]Regioselectivity in the Aryne Cross‐Coupling of Aryllithiums with Functionalized 1,2‐Dibromobenzenes
000087 (2011) Vincent Diemer [France] ; Frédéric R. Leroux [France] ; Françoise Colobert [France]Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2‐Dibromobenzenes
000139 (2010) Baptiste Manteau ; Pierre Genix [France] ; Lydia Brelot [France] ; Jean-Pierre Vors [France] ; Sergiy Pazenok [Allemagne] ; Florence Giornal ; Charlotte Leuenberger ; Frédéric R. LerouxA General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies
000241 (2007) Nadia M. Ahmad [Royaume-Uni] ; Vincent Rodeschini [Royaume-Uni] ; Nigel S. Simpkins [Royaume-Uni] ; Simon E. Ward [Royaume-Uni] ; Claire Wilson [Royaume-Uni]Synthetic studies towards garsubellin A: synthesis of model systems and potential mimics by regioselective lithiation of bicyclo[3.3.1]nonane-2,4,9-trione derivatives from catechinic acid
000278 (2007) Frédéric Leroux [France] ; Laurence Bonnafoux [France] ; Christophe Heiss [France] ; Françoise Colobert [France] ; Don Antoine Lanfranchi [France]A Practical Transition Metal‐Free Aryl‐Aryl Coupling Method: Arynes as Key Intermediates
000289 (2006) Paul Evans [Royaume-Uni] ; Paul Johnson [Royaume-Uni] ; Richard J. K. Taylor [Royaume-Uni]The Epoxy‐Ramberg–Bäcklund Reaction (ERBR): A Sulfone‐Based Method for the Synthesis of Allylic Alcohols
000293 (2006) Dimitris Kalaitzakis ; J. David Rozzell ; Ioulia Smonou [Grèce] ; Spiros KambourakisSynthesis of Valuable Chiral Intermediates by Isolated Ketoreductases: Application in the Synthesis of α‐Alkyl‐β‐hydroxy Ketones and 1,3‐Diols
000390 (2004) Toshiyuki Itoh [Japon] ; Kazutoshi Kudo [Japon] ; Kazuhisa Yokota [Japon] ; Naoko Tanaka [Japon] ; Shuichi Hayase ; Michel Renou [France]Synthesis and Biological Activity of Point‐Fluorinated Pheromone Analogues of Eldana saccharina
000521 (2001) Cristina Pesenti [Italie] ; Alberto Arnone [Italie] ; Stefano Bellosta [Italie] ; Pierfrancesco Bravo [Italie] ; Monica Canavesi [Italie] ; Eleonora Corradi [Italie] ; Massimo Frigerio [Italie] ; Stefano V. Meille [Italie] ; Mara Monetti [Italie] ; Walter Panzeri [Italie] ; Fiorenza Viani [Italie] ; Romina Venturini [Italie] ; Matteo Zanda [Italie]Total synthesis of a pepstatin analog incorporating two trifluoromethyl hydroxymethylene isosteres (Tfm-GABOB) and evaluation of Tfm-GABOB containing peptides as inhibitors of HIV-1 protease and MMP-9
000613 (2001) Cyril Papamicaël [France] ; Guy Quéguiner [France] ; Jean Bourguignon [France] ; Georges Dupas [France]A convenient synthesis of 3,4-difunctionalized δ-carbolines
000738 (2000) Sergio Pinheiro [Brésil] ; Clara B. S. S. Gonçalves [Brésil] ; Marcelo B. De Lima [Brésil] ; Florence M. C. De Farias [Brésil]A pinene-based chiral auxiliary for α-alkylation and aldol reactions: an unexpected effect of the base on the stereoselectivity
000B72 (1996) Thorsten Bach [Allemagne] ; Kai Jödicke [Allemagne] ; Birgit Wibbeling [Allemagne]Reversal of the facial diastereoselectivity in the Paternò-Büchi reaction of silyl enol ethers carrying a chiral substituent in α-position
001615 (1987) Yoshihiko Ikeda [Japon] ; Junzo Ukai [Japon] ; Nobuo Ikeda [Japon] ; Hisashi Yamamoto [Japon]Selective proton transfer of unsaturated esters
001762 (1985) L. Thijs [Pays-Bas] ; E. H. M. Stokkingreef [Pays-Bas] ; J. M. Lemmens [Pays-Bas] ; B. Zwanenburg [Pays-Bas]Enantio-controlled synthesis of the crocyclic C14-C23 subunit of cytochalasin b
001950 (1980) Gerald L. Larson ; Rafael Argülles ; Osvaldo Rosario ; Sydia SandovalThe preparation of α-hydroxyorganosilanes from α-borylorganosilane intermediates [1]

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