Serveur d'exploration sur le LRGP

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Le cluster Aziridine - Aziridines

Terms

5Aziridine
5Aziridines
4Lithiated terminal aziridines
8Hodgson
4Lithiated
10Ltmp
4Alkene

Associations

Freq.WeightAssociation
51.000Aziridine - Aziridines
40.894Aziridines - Lithiated terminal aziridines
40.894Aziridine - Lithiated terminal aziridines
50.791Aziridines - Hodgson
50.791Aziridine - Hodgson
40.707Hodgson - Lithiated terminal aziridines
30.671Aziridines - Lithiated
30.671Aziridine - Lithiated
40.632Lithiated terminal aziridines - Ltmp
40.566Aziridines - Ltmp
40.566Aziridine - Ltmp
50.559Hodgson - Ltmp
30.530Hodgson - Lithiated
30.530Alkene - Hodgson

Documents par ordre de pertinence
000074 (2006) David M. Hodgson [Royaume-Uni] ; Steven M. MilesDimerization of Lithiated Terminal Aziridines
000075 (2006) David M. Hodgson [Royaume-Uni] ; Steven M. MilesDimerization of Lithiated Terminal Aziridines
000066 (2007) David Hodgson [Royaume-Uni] ; Philip Humphreys ; Zhaoqing Xu ; John Ward [Royaume-Uni]Lithiation‐Induced Migrations from Nitrogen to Carbon in Terminal Aziridines
000067 (2007) David Hodgson [Royaume-Uni] ; Philip Humphreys ; Zhaoqing Xu ; John Ward [Royaume-Uni]Lithiation‐Induced Migrations from Nitrogen to Carbon in Terminal Aziridines
000048 (2009) Jianhui Huang [Royaume-Uni] ; Stephen P. Moore [Royaume-Uni] ; Peter O'Brien [Royaume-Uni] ; Adrian C. Whitwood [Royaume-Uni] ; John Gilday [Royaume-Uni]Lithiation-electrophilic trapping of N-sulfonyl-activated ethylene aziridines
000045 (2010) Joann Um ; Naeem Kaka ; David Hodgson [Royaume-Uni] ; K. Houk [États-Unis]Transition States and Origins of 1,4‐Asymmetric Induction in Alkylations of 2,2,6‐Trialkylpiperidine Enamines
000085 (2003) David M. Hodgson [Royaume-Uni] ; Nigel J. Reynolds [Royaume-Uni] ; Steven J. Coote [Royaume-Uni]Straightforward Synthesis of α,β‐Epoxysilanes from Terminal Epoxides by Lithium 2,2,6,6‐Tetramethylpiperidide‐Mediated Deprotonation‐in situ Silylation.
000049 (2009) Valerie Boissel [Royaume-Uni] ; Nigel S. Simpkinscurrent Address School Of Chemistry University Of Birmingham Edgbaston Birmingham Uk B15 Tt. [Royaume-Uni] ; Gurdip Bhalay [Royaume-Uni] ; Alexander J. Blake [Royaume-Uni] ; William Lewis [Royaume-Uni]Bridgehead enolates and bridgehead alkenes in a welwistatin model series
000053 (2008) Ahmed Naama [Royaume-Uni] ; Claire Haven-Tang [Royaume-Uni] ; Eleri Jones [Royaume-Uni]Human resource development issues for the hotel sector in Libya: a government perspective
000064 (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
000068 (2007) Robert Mulvey [Royaume-Uni] ; Florence Mongin [France] ; Masanobu Uchiyama [Japon] ; Yoshinori Kondo [Japon]Deprotonative Metalation Using Ate Compounds: Synergy, Synthesis, and Structure Building
000078 (2005) Jason Eames [Royaume-Uni] ; Michael J. SuggateRecent Developments in the Transfer of Chirality within Enolate Alkylation Reactions
000083 (2004) David M. Hodgson [Royaume-Uni] ; Frédéric Le Strat [Royaume-Uni]Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid
000107 (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
000114 (1997) Jean-Marie Beau [France] ; Timothy Gallagher [Royaume-Uni]Nucleophilic C-glycosyl donors for C-glycoside synthesis

Wicri

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