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Volumn 16, Issue 13, 2010, Pages 4048-4062

Preparation of "Si-centered" chiral silanes by direct α-lithiation of methylsilanes

Author keywords

Chirality; Lithium; Organolithium compounds; Organosilicon; Structure elucidation

Indexed keywords

ALKYLLITHIUMS; ALTERNATIVE ROUTES; CHIRAL COMPOUNDS; CHIRAL SILANES; COMPUTATIONAL STUDIES; DESYM-METRIZATION; DIASTEREO-SELECTIVITY; EFFICIENT METHOD; HIGH YIELD; LITHIATION; METHYL GROUP; METHYLSILANES; OLIGOSILANES; ORGANOLITHIUM COMPOUNDS; ORGANOSILICONES; REPULSION EFFECTS; SILICON CENTERS; STRUCTURE ANALYSIS; STRUCTURE ELUCIDATION; STRUCTURE FORMATIONS; TRANSITION STATE; X RAY STRUCTURE ANALYSIS;

EID: 77950246389     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200902551     Document Type: Article
Times cited : (17)

References (124)
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    • note
    • 1HNMR resonance signals of the trimethylstannyl group in which could be integrated separately. Comparison of the spectra of the racemic and enantiomerically pure compounds gave an e.r. of >99:1 as no signal, due to the second possible diastereomer was detected.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.