Highly diastereoselective addition of n-boc-pyrroiidin-2-yiiithium to optically active ketimines -Synthesis of enantiomerically pure l,3-imidazoiidin-2-ones and diamines

European Journal of Organic Chemistry

Volumn , Issue 2, 2002, Pages 301-308

  Keyserlingk, Nikolai Graf V ^a   Martens, Jürgen ^a  

^a UNIVERSITY OF OLDENBURG   (Germany)

Author keywords

C c coupling; Diastereoselectivity; Ligand design; Nitrogen heterocycles; Schiff bases

Indexed keywords

CRYSTAL STRUCTURE; CYCLIZATION; NITROGEN; STEREOSELECTIVITY;

C-C COUPLING; DIASTEREOSELECTIVE ADDITIONS; DIASTEREOSELECTIVITIES; IMIDAZOLIDIN; KETIMINES; LIGAND DESIGN; NITROGEN HETEROCYCLES; OPTICALLY ACTIVE; SCHIFF-BASE; SYNTHESISED;

KETONES;

1,3 IMIDAZOLIDIN 2 ONE; DIAMINE; N BOC PYRROLIDIN 2 YL LITHIUM; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CRYSTAL STRUCTURE; CYCLIZATION; DECOMPOSITION; DIASTEREOISOMER; ENANTIOMER; HYDROLYSIS; OPTICAL ROTATION; RACEMIC MIXTURE; REACTION ANALYSIS; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 0036153770     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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