Ouverture d'oxirannes et d'oxetannes par des organolithiens fluorovinyliques en presence de BF3.Et2O

DOI: 10.1016/0022-328X(88)89059-4

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Journal of Organometallic Chemistry p. 11 - 18 (1988)

Update date:2022-08-11

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Authors:

Dubuffet, Thierry

Sauvetre, Raymond

Normat, Jean-F.

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Article abstract of DOI:10.1016/0022-328X(88)89059-4

BF3.Et2O promotes the nucleophilic addition of various fluorovinyllithium reagents to oxiranes and oxetanes. γ-and δ-fluoro unsaturated alcohols were obtained.

Full text of DOI:10.1016/0022-328X(88)89059-4

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Article Doi

Ouverture d'oxirannes et d'oxetannes par des organolithiens fluorovinyliques en presence de BF3.Et2O

DOI: 10.1016/0022-328X(88)89059-4

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0022-328X(88)89059-4

Full text of DOI:10.1016/0022-328X(88)89059-4

Products guided by the article

R&D Labs maybe for 109993-33-1

Relevant to this article

Isolation, structure elucidation, and KDD study of (-)-Celosine, a new skeleton with potent anti-atherosclerosis activity

Switch-on fluorescent/FRET probes to study human histidine triad nucleotide binding protein 1 (hHint1), a novel target for opioid tolerance and neuropathic pain

Acid catalysis of the photochemical deconjugation reaction of 3-alkyl-2-cyclohexenones

Design, Synthesis and Biological Evaluation of Ferrocenyl Thiazole and Thiazolo[5,4- d]thiazole Catechols as Inhibitors of 5-hLOX and as Antibacterials against Staphylococcus aureus. Structural Relationship and Computational Studies

Alkylation of 5,10,15-tris(3,5-di-t-butyl-4-hydroxyphenyl)-20-(4-pyridyl)porphyrin

The Synthesis of Alkyl and (Hetero)aryl Sulfonamides from Sulfamoyl Inner Salts