Synthesis of enantioenriched tertiary benzylic alcohols via stereospecific lithiation of secondary benzyl carbamates - Design of dialkylcarbamates, cleavable under basic, mild conditions

Synthesis

Volumn , Issue 1, 1996, Pages 149-154

  Derwing, Christoph ^a   Hoppe, Dieter ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

chiral configurationally stable ion pairs; enantioselective synthesis; lithiated benzyl carbamates; O protecting groups; stereospecificity of electrophilic substitution; tertiary benzylic alcohols

Indexed keywords

ALKANOL; CARBAMIC ACID DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; INFRARED SPECTROPHOTOMETRY; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030069953     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1996-4163     Document Type: Article

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