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Two efficient methods for the cleavage of pinanediol boronate esters yielding the free boronic acids

Author
COUTTS, S. J; ADAMS, J; KORLIKOWSKI, D; SNOW, R. J
Boerhinger Ingelheim Pharmaceuticals Inc., dep. medicinal chemistry, Ridgefield CT 06877-0368, United States
Source

Tetrahedron letters. 1994, Vol 35, Num 29 ; 5091, 5109-5112 [5 p.] ; ref : 9 ref

CODEN
TELEAY
ISSN
0040-4039
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Aminoamide Chlorhydrate Déprotection Hydrogène Chlorure Pyrrolidine dérivé Sodium Periodate α-Aminoacide 4,6-Méthano-1,3,2-benzodioxaborole2-[1-prolylpyrrolidin-2-yl] 4,6-Méthano-1,3,2-benzodioxaborole(perhydro-2-[1-prolylpyrrolidin-2-yl]-3a,8,8-triméthyl) Borane(dihydroxy phényl) Boronique acide dérivé Proline pyrrolidide [2-(dihydroxy boryl)]
Keyword (en)
Aminoamide Hydrochlorides Deprotection Hydrogen Chlorides Pyrrolidine derivatives Sodium Periodates α-Aminoacid
Keyword (es)
Aminoamida Hidrocloruro Desprotección Hidrógeno Cloruro Sodio Periodato α-Aminoácido
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4156558

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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