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Serveur d'exploration sur le LRGP - Curation (Istex)

Index « Keywords » - entrée « Grignard »
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List of bibliographic references

Number of relevant bibliographic references: 14.
Ident.Authors (with country if any)Title
000345 (1995) P. A. Lander [États-Unis] ; L. S. Hegedus [États-Unis]ChemInform Abstract: Asymmetric Synthesis of α‐Amino Acids by Copper‐Catalyzed Conjugate Addition of Grignard Reagents to Optically Active Carbamatoacrylates.
001303 (2011) Majid Khalil Syed ; Mike Casey [Irlande (pays)]Enantioselective Synthesis of Benzyl tert‐Butyl Sulfoxides
001849 (2001) Christelle Lauret [Royaume-Uni]Epoxy ketones as versatile building blocks in organic synthesis
001915 (1991) Tadao Shibutani [Japon] ; Hisashi Fujihara [Japon] ; Naomichi Furukawa [Japon] ; Shigeru Oae [Japon]Ligand exchange reactions of aryl pyridyl sulfoxides with grignard reagents: Convenient preparation of 3‐ and 4‐pyridyl grignard reagents and examination of the leaving abilities of pyridyl anions
001A52 (1989) Gerald L. Larson [États-Unis]Organosilicon survey 1986-the SiliconCarbon bond
001C11 (2005) Ben Conway [Royaume-Uni] ; Eva Hevia [Royaume-Uni] ; Alan R. Kennedy [Royaume-Uni] ; Robert E. Mulvey [Royaume-Uni] ; Susan Weatherstone [Royaume-Uni]Synthesis and characterisation of a series of alkylmagnesium amide and related oxygen-contaminated “alkoxy” compounds
001C19 (2006) Organolithium and organomagnesium compounds of the naphthalene series in organic synthesis
001C25 (1986) G. Pattenden ; D. W. KnightCarboxylic acids and derivatives
001C30 (1994) D. W. KnightSynthetic approaches to butenolides
001C41 (1979) D. R. Hogg ; D. R. Hogg ; P. Metzner ; J. Voss ; W. WalterThiocarbonyl and selenocarbonyl compounds
001C55 (1990) G. Pattenden ; T. N. Danks ; S. E. Thomas ; T. GallagherOrganometallics in synthesis
001C63 (1988) S. R. DrakeChapter 2. Li, Na, K, Rb, Cs; Be, Mg, Ca, Sr, Ba
001C64 (1999) Kamyar AfarinkiaMain group organometallics in organic synthesis
001C82 (2008) Chapter 6 - Asymmetric Synthesis with Stereodynamic Compounds: Introduction, Conversion and Transfer of Chirality

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