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Volumn 69, Issue 29, 2013, Pages 5823-5828

Chirality transfer in Brook rearrangement-mediated SE2′ solvolytic protonation and its use in estimation of the propensity for racemization of the α-lithiocarbanions of the substituents

Author keywords

Carbanion; Chirality transfer; Electrophilic substitution; Rearrangement

Indexed keywords

ALCOHOL DERIVATIVE; ALPHA LITHIOCARBANION DERIVATIVE; ELECTROPHILE; LITHIUM DERIVATIVE; SILICATE; SOLVENT; UNCLASSIFIED DRUG;

EID: 84878839716     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.043     Document Type: Article
Times cited : (11)

References (76)
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    • Regarding description of enantioselectivities, we use "ee" rather than "er" throughout this article for the sake of convenience for comparison in Table 3, although the former seems to be replacing by the latter ()
    • Regarding description of enantioselectivities, we use "ee" rather than "er" throughout this article for the sake of convenience for comparison in Table 3, although the former seems to be replacing by the latter (R.E. Gawley J. Org. Chem. 71 2006 2411 2416)
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    • To our knowledge, there are no reports on a direct comparison of the reactivity and the configurational stability among metallocarbanions where the metal cation is lithium, sodium, or potassium. For the reactivity of the corresponding enolates, see
    • To our knowledge, there are no reports on a direct comparison of the reactivity and the configurational stability among metallocarbanions where the metal cation is lithium, sodium, or potassium. For the reactivity of the corresponding enolates, see: H.D. Zook, and W.L. Gumby J. Am. Chem. Soc. 82 1960 1386 1389
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.