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Volumn 137, Issue 19, 2015, Pages 6335-6349

Alkenes as alkyne equivalents in radical cascades terminated by fragmentations: Overcoming stereoelectronic restrictions on ring expansions for the preparation of expanded polyaromatics

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; CHEMICAL BONDS; CYCLIZATION; NAPHTHALENE; TIN;

EID: 84930225180     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b02373     Document Type: Article
Times cited : (83)

References (164)
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    • This concept provides an interesting counterpart to "pools of cations", an elegant concept introduced by Yoshida and co-workers
    • This concept provides an interesting counterpart to "pools of cations", an elegant concept introduced by Yoshida and co-workers: Okajima, M.; Suga, S.; Itami, K.; Yoshida, J.-i. J. Am. Chem. Soc. 2005, 127, 6930
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    • For such strong interactions, energies are sensitive to orbital overlap. When the vicinal acceptor center is separated from the donor by a double bond, the shorter distance between the interacting groups enhances orbital overlap. See
    • For such strong interactions, energies are sensitive to orbital overlap. When the vicinal acceptor center is separated from the donor by a double bond, the shorter distance between the interacting groups enhances orbital overlap. See: Alabugin, I. V.; Zeidan, T. A. J. Am. Chem. Soc. 2002, 124, 3175
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    • Additional factors, such as transition state aromaticity, come into play for anionic endo-cyclizations. See
    • Additional factors, such as transition state aromaticity, come into play for anionic endo-cyclizations. See: Gilmore, K.; Manoharan, M.; Wu, J.; Schleyer, P. v. R.; Alabugin, I. V. J. Am. Chem. Soc. 2012, 134, 10584
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.