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Cdcl < Cdcl3 < Cddp  Facettes :

List of bibliographic references indexed by Cdcl3

Number of relevant bibliographic references: 62.
[40-60] [0 - 20][0 - 50][60-61][60-80]
Ident.Authors (with country if any)Title
001858 (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
001866 (2001) Christine Hemmerlin [France] ; Manh Thong Cung [France] ; Guy Boussard [France]Synthesis and conformational preferences in solution and crystalline states of an aza-tripeptide
001917 (2001) Toshimasa Katagiri [Japon] ; Michiharu Handa [Japon] ; Yasuhisa Matsukawa [Japon] ; J. S. Dileep Kumar [Japon] ; Kenji Uneyama [Japon]Efficient synthesis of an optically pure β-bromo-β,β-difluoroalanine derivative, a general precursor for β,β-difluoroamino acids
001941 (2001) Renato Dalpozzo [Italie] ; Giuseppe Bartoli ; Marcella Bosco [Italie] ; Antonio De Nino ; Antonio Procopio ; Letizia Sambri [Italie] ; Antonio TagarelliAn Efficient Diastereoselective Reduction of α‐Alkyl‐β‐keto Carbonitriles with TiCl4/BH3 or LiBH4/CeCl3 to syn‐ or anti‐α‐Alkyl‐β‐hydroxy Carbonitriles
001948 (2001) Corinne Fruit [France] ; Alain Turck [France] ; Nelly Plé [France] ; Ljubica Mojovic [France] ; Guy Quéguiner [France]A new route to Septorin via controlled metalations of pyrazines. Diazines XXX
001950 (2001) Cyril Papamicaël [France] ; Guy Quéguiner [France] ; Jean Bourguignon [France] ; Georges Dupas [France]A convenient synthesis of 3,4-difunctionalized δ-carbolines
001A75 (2000) Michael J. Broadhurst [Royaume-Uni] ; Samantha J. Brown [Royaume-Uni] ; Jonathan M. Percy [Royaume-Uni] ; Michael E. Prime [Royaume-Uni]Synthesis of α-hydroxy-β,β-difluoro-γ-ketoesters via [3,3]sigmatropic rearrangements
001B21 (2000) Mouhsine Lourak [Maroc] ; Régis Vanderesse [France] ; André Vicherat [France] ; Jamal Jamal-Eddine [Maroc] ; Michel Marraud (chimiste) [France]The carbonylhydrazone pseudopeptide link via quinonic oxidation of the peptide amino terminus
001B25 (2000) V. Gautheron Chapoulaud [France] ; N. Plé [France] ; A. Turck [France] ; G. Quéguiner [France]Synthesis of 4,8-Diarylcinnolines and Quinazolines with Potential Applications in Nonlinear Optics. Diazines. Part 28
001B32 (2000) C. Didierjean [France] ; André Aubry (chimiste) [France] ; F. Wyckaert [France] ; G. Boussard [France]Structural features of thePip/AzPip couple in the crystalline state: influence of the relative AzPip location in an azadipeptide sequence upon the induced chirality and conformational characteristics
001B39 (2000) Surajit Sinha [Inde] ; Bhubaneswar Mandal [Inde] ; Srinivasan Chandrasekaran [Inde]Selective para metalation of unprotected 3-methoxy and 3,5-dimethoxy benzoic acids with n- butyl lithium–potassium tert -butoxide (LIC–KOR): synthesis of 3,5-dimethoxy-4-methyl benzoic acid
001B41 (2000) Olivier Legrand [France] ; Jean Michel Brunel [France] ; Gérard Buono [France]Scope and Limitations of the Aromatic Anionic [1,3] P–O to P–C Rearrangement in the Synthesis of Chiral o -Hydroxyaryl Diazaphosphonamides
001B78 (2000) Renato Dalpozzo [Italie] ; Antonio De Nino [Italie] ; Daniela Miele [Italie] ; Antonio Procopio [Italie] ; Antonio Tagarelli [Italie] ; Giuseppe Bartoli [Italie]Dianions of acyclic β‐enamino ketones and electrophiles. 9. Synthesis and reactivity of phosphorylated enaminones
001B86 (2000) Hiroki Kumamoto [Japon] ; Satoru Shindoh [Japon] ; Hiromichi Tanaka [Japon] ; Yoshiharu Itoh [Japon] ; Kazuhiro Haraguchi [Japon] ; Eisen Gen [Japon] ; Atsushi Kittaka [Japon] ; Tadashi Miyasaka [Japon] ; Masato Kondo [Japon] ; Kazuo T. Nakamura [Japon]An Intramolecular Anionic Migration of a Stannyl Group from the 6-Position of 1-(2-Deoxy-d- erythro -pent-1-enofuranosyl)uracil to the 2′-Position: Synthesis of 2′-Substituted 1′,2′-Unsaturated Uridines
001B91 (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
001C52 (1999) Azhar Ariffin ; Alexander J. Blake ; Mark R. Ebden ; Wan-Sheung Li ; Nigel S. Simpkins ; David N. A. FoxThe diastereoselective and enantioselective substitution reactions of an isoindoline–borane complex
001C53 (1999) Xuedong Dai [États-Unis] ; Scott Virgil [États-Unis]Synthesis of 2-heterosubstituted quinazolinone atropisomeric phosphine ligands by direct lithiation of a 2-unsubstituted quinazolinone system
001D02 (1999) Anne Jonquières [France] ; André Vicherat [France] ; Pierre Lochon [France]Synthesis and characterization of new polyamideimides with a highly flexible soft block
001D32 (1999) Carlos Cativiela [Espagne] ; María D. Díaz-De-Villegas [Espagne] ; Ana I. Jiménez [Espagne] ; Pilar L Pez [Espagne] ; Michel Marraud (chimiste) [France] ; Laureano Oliveros [France]Efficient access to all four stereoisomers of phenylalanine cyclopropane analogues by chiral HPLC
001F55 (1998) H. A. M. Van Mullekom ; J. A. J. M. Vekemans ; E. W. Meijer [Pays-Bas]Band‐Gap Engineering of Donor–Acceptor‐Substituted π‐Conjugated Polymers
002129 (1997) Richard A. Ewin ; Angus M. Macleod ; David A. Price ; Nigel S. Simpkins ; Alan P. WattChiral base mediated asymmetric synthesis oftricarbonyl(η6-arene)chromium complexes

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