Utilisation du groupe allyle comme groupe protecteur d'amines Application à la synthése de la biotine

Tetrahedron Letters

Volumn 18, Issue 30, 1977, Pages 2591-2594

  Moreau, Bernard ^a   Lavielle, Solange ^a   Marquet, Andrée ^a  

^a CNRS CERCOA 2 à ^*  (France)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN;

CHROMATOGRAPHY; DIALLYLBIOTIN; DRUG ANALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; IN VITRO STUDY; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; THEORETICAL STUDY;

EID: 0017383282     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)83828-4     Document Type: Article

References (16)

1. Isomerisation of allyl phenyl ethers and allylphenols with transition metal catalysts
2. The allyl ether as a protecting group in carbohydrate chemistry. Isomerisations with tristriphenylphosphinerhodium(I) chloride
3. Products formed from rhodium trichloride trihydrate and allyl alcohol or diallyl ether; the crystal and molecular structure of [Rh2Cl4(C6H11O)2],CH3OH
4. Cleavage of Allyl Ethers with Pd/C
5. 1190. Chemistry of the metal carbonyls. Part XXXII. Isomerisation of allyl compounds and the dimerisation of norbornadiene
6. Catalysed prototropic rearrangements. Part II. Metal carbonyl-catalysed isomerization of N-allylamides to prop-2-enyl derivatives
7. Hydrogen Transfer from Organic Compounds Catalysed by Transition Metal Complexes
8. The preparation and properties of tris(triphenylphosphine)halogenorhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivatives