1–10 of 10

  1. Aldehydes from 4,4-dimethyl-2-oxazoline and Grignard reagents: o-anisaldehydeOrganometallic addition Org. Synth. Coll. Vol. 6, p. 64; Vol. 54, p. 42 · Brinkmeyer et al.
  2. Cross-Coupling of Alkenyl/Aryl Carboxylates with Grignard Reagents via Fe-Catalyzed C-O Bond ActivationOrganometallic addition Org. Synth. Vol. 91, p. 83 · Li et al.
  3. Formyl transfer to Grignard reagents with N-formylpiperidine: 3-phenylpropionaldehydeOrganometallic addition Org. Synth. Coll. Vol. 7, p. 451; Vol. 64, p. 114 · Olah and Arvanaghi
  4. Highly reactive magnesium for the preparation of Grignard reagents: 1-norbornanecarboxylic acidOrganometallic addition Org. Synth. Coll. Vol. 6, p. 845; Vol. 59, p. 85 · Rieke et al.
  5. Iron-Catalyzed Selective Conjugate Addition of Aryl Grignard Reagents to 2,4-Alkadienoates: tert-Butyl (Z)-5-Phenyl-3-hexenoateOrganometallic addition Org. Synth. Vol. 91, p. 307 · Hata et al.
  6. Ketones from carboxylic acids and Grignard reagents: methyl 6-oxodecanoateOrganometallic addition Org. Synth. Coll. Vol. 8, p. 441; Vol. 66, p. 116 · Fujisawa and Sato
  7. Nickel-catalyzed coupling of aryl O-carbamates with Grignard reagents: 2,7-dimethylnaphthaleneOrganometallic addition Org. Synth. Vol. 78, p. 42 · Dallairea et al.
  8. Nucleophilic hydroxymethylation by the (isopropoxydimethylsilyl)methyl Grignard reagent: 1-(hydroxymethyl)cyclohexanol from cyclohexanoneOrganometallic addition Org. Synth. Coll. Vol. 8, p. 315; Vol. 69, p. 96 · Tamao et al.
  9. Phosphine–nickel complex catalyzed cross-coupling of Grignard reagents with aryl and alkenyl halides: 1,2-dibutylbenzeneOrganometallic addition Org. Synth. Coll. Vol. 6, p. 407; Vol. 58, p. 127 · Kumada et al.
  10. Use ofcerium(III) chloride in the reactions of carbonyl compounds with organolithiums or Grignard reagents for the suppression of abnormal reactions:1-butyl-1,2,3,4-tetrahydro-1-naphtholOrganometallic addition Org. Synth. Vol. 76, p. 228 · Takeda and Imamoto