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Index « ISSN » - entrée « 1433-7851 »
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1432-2072 < 1433-7851 < 1433-8491  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 20.
Ident.Authors (with country if any)Title
000046 (2012) Donato Ivan Coppi [Italie] ; Antonio Salomone [Italie] ; Filippo Maria Perna [Italie] ; Vito Capriati [Italie]Exploiting the Lithiation‐Directing Ability of Oxetane for the Regioselective Preparation of Functionalized 2‐Aryloxetane Scaffolds under Mild Conditions
000124 (2010) David Hodgson [Royaume-Uni] ; Johannes KloesgesLithiation–Electrophilic Substitution of N‐Thiopivaloylazetidine
000128 (2010) Frédérique Battin-Leclerc [France] ; Olivier Herbinet [France] ; Pierre-Alexandre Glaude [France] ; René Fournet [France] ; Zhongyue Zhou [République populaire de Chine] ; Liulin Deng [République populaire de Chine] ; Huijun Guo [République populaire de Chine] ; Mingfeng Xie [République populaire de Chine] ; Fei Qi [République populaire de Chine]Experimental Confirmation of the Low‐Temperature Oxidation Scheme of Alkanes
000138 (2010) Koichi Mikami [Japon] ; Yuichi Tomita [Japon] ; Yoshimitsu Itoh [Japon]Activation of CF Bonds in Preference to CI Bonds: Difluoromethylation of Lithium Enolates with Trifluoromethyl Iodide
000168 (2009) Graphical Abstract: Angew. Chem. Int. Ed. 6/2009
000200 (2008) Doris Chun [États-Unis] ; Yang Cheng [États-Unis] ; Fred Wudl [États-Unis]The Most Stable and Fully Characterized Functionalized Heptacene
000231 (2008) Todd Macklin ; Jane Panteleev [Canada] ; Victor Snieckus [Canada]Carbamoyl Translocations by an Anionic ortho‐Fries and Cumulenolate α‐Acylation Pathway: Regioselective Synthesis of Polysubstituted Chromone 3‐ and 8‐Carboxamides
000237 (2008) Satinder Kessar [Inde] ; Paramjit Singh ; Kamal Singh ; Prasad Bharatam ; Arvind Sharma ; Sneh Lata ; Amarjit KaurA Study of BF3‐Promoted ortho Lithiation of Anilines and DFT Calculations on the Role of Fluorine–Lithium Interactions
000259 (2007) David Hodgson [Royaume-Uni] ; Philip Humphreys ; Zhaoqing Xu ; John Ward [Royaume-Uni]Lithiation‐Induced Migrations from Nitrogen to Carbon in Terminal Aziridines
000266 (2007) Robert Mulvey [Royaume-Uni] ; Florence Mongin [France] ; Masanobu Uchiyama [Japon] ; Yoshinori Kondo [Japon]Deprotonative Metalation Using Ate Compounds: Synergy, Synthesis, and Structure Building
000320 (2006) David M. Hodgson [Royaume-Uni] ; Steven M. MilesDimerization of Lithiated Terminal Aziridines
000340 (2005) Jason Eames [Royaume-Uni] ; Michael J. SuggateRecent Developments in the Transfer of Chirality within Enolate Alkylation Reactions
000348 (2005) Graphical Abstract: Angew. Chem. Int. Ed. 2/2005
000462 (2002) Vincent Semetey ; Didier Rognan [France] ; Christine Hemmerlin [France] ; Roland Graff [France] ; Jean-Paul Briand ; Michel Marraud (chimiste) [France] ; Gilles Guichard [France]Stable Helical Secondary Structure in Short‐Chain N,N′‐Linked Oligoureas Bearing Proteinogenic Side Chains
000526 (2001) Brian R. Bear [États-Unis] ; Steven M. Sparks [États-Unis] ; Kenneth J. Shea [États-Unis]The Type 2 Intramolecular Diels–Alder Reaction: Synthesis and Chemistry of Bridgehead Alkenes
000661 (2000) Dietmar Kuck [Allemagne]Thermochemical Data of Organic Ions Obtained from Investigations in the More or Less “Diluted” Gas Phase
000818 (1999) Susumu Saito ; Masahito Shiozawa ; Hisashi Yamamoto [Japon]Mixed Crossed Aldol Condensation between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6‐diphenylphenoxide)
000937 (1998) Holger Braunschweig [Allemagne] ; Carsten Kollann ; Ulli EnglertSynthesis and Structure of the First Terminal Borylene Complexes
000940 (1998) Alan R. Kennedy ; Robert E. Mulvey [Royaume-Uni] ; René B. RowlingsRemarkable Reaction of Hetero‐S‐Block‐Metal Amides with Molecular Oxygen: Cationic (NMNMg)2 Ring Products (M=Li or Na) with Anionic Oxo or Peroxo Cores
000967 (1998) Susumu Saito ; Keiko Hatanaka ; Taichi Kano ; Hisashi Yamamoto [Japon]Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6‐Bis(2‐isopropylphenyl)‐3,5‐dimethylphenol as an Extremely Effective Chiral Auxiliary

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