Serveur d'exploration sur le LRGP - Analysis (UK)

Index « Auteurs » - entrée « David M. Hodgson »
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List of bibliographic references

Number of relevant bibliographic references: 9.
Ident.Authors (with country if any)Title
000026 (2012) David M. Hodgson [Royaume-Uni] ; Rosanne S D. Persaud [Royaume-Uni]Alkenes from β-lithiooxyphosphonium ylides generated by trapping α-lithiated terminal epoxides with triphenylphosphine
000042 (2010) David M. Hodgson [Royaume-Uni] ; Zhaoqing Xu [Royaume-Uni]α,β-Aziridinylphosphonates by lithium amide-induced phosphonyl migration from nitrogen to carbon in terminal aziridines
000061 (2007) David M. Hodgson [Royaume-Uni] ; Matthew J. Fleming ; Steven J. StanwayThe reactivity of epoxides with lithium 2,2,6,6-tetramethylpiperidide in combination with organolithiums or grignard reagents.
000062 (2007) David M. Hodgson [Royaume-Uni] ; Ying Kit Chung ; Irene Nuzzo ; Gloria Freixas ; Krystyna K. Kulikiewicz ; Ed Cleator ; Jean-Marc ParisIntramolecular cyclopropanation of unsaturated terminal epoxides and chlorohydrins.
000063 (2007) David M. Hodgson [Royaume-Uni] ; Philip G. Humphreys ; Steven M. Miles ; Christopher A J. Brierley ; John G. WardDimerization and isomerization reactions of alpha-lithiated terminal aziridines.
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
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
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.

List of associated KwdEn.i

Nombre de
documents
Descripteur
4Chem
4Hodgson
4Tetrahedron
3Dimerization
3Lett
3Ltmp
3Molecular Structure
3Tetrahedron lett
2Alkene
2Angew
2Aziridine
2Aziridines
2Enantiopure
2Enantiopure substrates
2Epoxy Compounds (chemistry)
2Isomer
2Lithiated
2Lithiated aziridines
2Lithiated terminal aziridines
2Protease
2Protease inhibitors
2Stereoisomerism
2Verlag gmbh
1Acetates (chemistry)
1Aldehydes (chemistry)
1Alkenes (chemistry)
1Allene
1Amides (chemistry)
1Amines (chemical synthesis)
1Amines (chemistry)
1Aziridines (chemistry)
1Base terminal epoxides
1Bicyclo Compounds (chemistry)
1Carbonyl
1Catalysis
1Chlorohydrins (chemistry)
1Commun
1Coote
1Cycloaddition
1Cycloadduct
1Cyclopropanes (chemical synthesis)
1Cyclopropanes (chemistry)
1Derivative
1Deuterium (chemistry)
1Dodecanol (analogs & derivatives)
1Dyson
1Dyson perrins
1Epoxides
1Epoxysilanes
1Equiv
1Esters (chemical synthesis)
1Esters (chemistry)
1Heptanes (chemistry)
1Hexanes (chemistry)
1Hydrogenation
1Isomerism
1Lithium (chemistry)
1Lithium Compounds (chemistry)
1Nemorensic
1Nemorensic acid
1Organometallic Compounds
1Organometallic Compounds (chemical synthesis)
1Organometallic Compounds (chemistry)
1Oxirane
1Oxirane derivatives oxirane derivatives
1Oxiranyllithium
1Perkin trans
1Perrins
1Pyridines (chemistry)
1Sesquiterpenes (chemical synthesis)
1Sesquiterpenes (chemistry)
1Sex Attractants
1Silanes (chemistry)
1Silylated
1Silylation
1Straightforward synthesis
1Terminal epoxides
1Univ
1Ylide

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