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Volumn 73, Issue 24, 2008, Pages 9647-9656

Stereoselective alkylations of chiral nitro imine and nitro hydrazone dianions. Synthesis of enantiomerically enriched 3-substituted 1-nitrocyclohexenes

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATIONS; ALKYLATION PRODUCTS; CHEMICAL EQUATIONS; DI ANIONS; DIASTEREOSELECTIVE ALKYLATIONS; HYDRAZONE; METALLOENAMINES; STEREOSELECTIVE; STERIC DIFFERENCES;

EID: 58049204533     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801790r     Document Type: Article
Times cited : (9)

References (117)
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    • A reviewer has suggested that a Li-π-naphthalene coordination might be responsible for the preferred conformation of the stereocontrolling group. In a simple calculation, it was found that the cyclohexene ring in the dianion is not planar and pseudoaxial hydrogens may also contribute to the direction of electrophilic attack. We thank the reviewer for this suggestion
    • A reviewer has suggested that a Li-π-naphthalene coordination might be responsible for the preferred conformation of the stereocontrolling group. In a simple calculation, it was found that the cyclohexene ring in the dianion is not planar and pseudoaxial hydrogens may also contribute to the direction of electrophilic attack. We thank the reviewer for this suggestion.


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