Synthesis and Structure of a Monomeric Chiral Lithium Dialkylaluminium Amide Derived from Schöllkopf’s Bis‐lactim Ether and α‐(Methylbenzyl)benzylamine | Zendy

Andrews Philip C. | Zendy; Maguire Melissa | Zendy; PomboVillar Esteban | Zendy

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Synthesis and Structure of a Monomeric Chiral Lithium Dialkylaluminium Amide Derived from Schöllkopf’s Bis‐lactim Ether and α‐(Methylbenzyl)benzylamine

Author(s) -

Andrews Philip C.,

Maguire Melissa,

PomboVillar Esteban

Publication year - 2003

Publication title -

european journal of inorganic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.667

H-Index - 136

eISSN - 1099-0682

pISSN - 1434-1948

DOI - 10.1002/ejic.200300186

Subject(s) - chemistry , benzylamine , amide , lithium amide , ether , monomer , lithium (medication) , trimethylsilyl , pyrazine , crystal structure , stereochemistry , medicinal chemistry , polymer chemistry , organic chemistry , catalysis , enantioselective synthesis , medicine , polymer , endocrinology

Crystals of a monomeric lithium dialkylaluminium amide containing two different chiral amide moieties have been isolated from the reaction of lithiated Schöllkopf’s bis‐lactim ether complexed by pmdta with the diethylaluminium amide of ( S )‐α‐(methylbenzyl)benzylamine, with single crystal X‐ray diffraction revealing a migration of the Li cation in the aluminate from its initial position on the pyrazine ring of the lactim ether precursor. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

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