Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Bernard Mauze"'
Autor:
Laurent Sarrazin, Bernard Mauze
Publikováno v:
Synthetic Communications. 26:3179-3191
Coupling of aldehydes with 3-bromo-1-cyano-1-propene, using indium in water, is a very convenient method to prepare α-cyano-β-ethylenic secondary alcohols.
Autor:
Léone Miginiac, Bernard Mauze
Publikováno v:
ChemInform. 22
Autor:
Bernard Mauze, Laurent Sarrazin
Publikováno v:
ChemInform. 27
Coupling of aldehydes with 3-bromo-1-cyano-1-propene, using indium in water, is a very convenient method to prepare α-cyano-β-ethylenic secondary alcohols.
Autor:
Léone Miginiac, Bernard Mauze
Publikováno v:
Journal of Organometallic Chemistry. 411:69-74
Lithiated trimethylsilylacetonitrile easily reacts, at −78°C, with various alkyl bromides to lead to α-functional trimethylsilanes RCH(SiMe3)CN, with R a saturated or unsaturated group.
Publikováno v:
ChemInform. 36
A new carbohydrate nitrone intramolecular cycloaddition reaction is described for the enantioselective synthesis of bicyclic oxazolidines. By choice of the precursor, the products possess a chiral quaternary bridgehead aryl substitution. Also describ
Publikováno v:
ChemInform. 36
A new methodology is described for the rapid enantiomeric synthesis of a novel series of pyranopyrrolidines from readily available and inexpensive carbohydrate compounds. The major feature of the method is a highly selective [3+2] cycloaddition react
Autor:
Bernard Mauze
Publikováno v:
Journal of Organometallic Chemistry. 134:1-13
Allyl-magnesium, -lithium and saturated lithium compounds undergo addition reactions with conjugated and α-functional enynes or diynes: R″′ C 4 C 3 C 2 H C 1 HC(R)(R′)Y;R″′ C 4 H C 3 H C 2 C 1 (R)(R′)Y;R'″′ C 4 (Y =
Publikováno v:
Journal of Organometallic Chemistry. 72:309-322
Reactive organometallic compounds such as allyl-zinc, -magnesium, and -lithium and saturated lithium compounds are shown to bring about readily an addition reaction with simple and α-substituted conjugated enynes RCCCHCHCH2 R′ [R
Publikováno v:
Journal of Organometallic Chemistry. 368:1-18
Organozinc and organoaluminum compounds derived from propargylic or allylic bromides react regioselectively with β-ketotriazoles to give the novel 1-aryl-2-triazolyl-1 ethanols which are potential fungicides.
Autor:
Bernard Mauze
Publikováno v:
Journal of Organometallic Chemistry. 202:233-239
N-substituted α-ethylenic aziridines are easily prepared by treating gem-chloro-(methyl)allyllithium with aldimines and ketimines.