1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
about
Exploration of cascade cyclizations terminated by tandem aromatic substitution: total synthesis of (+)-schweinfurthin A.A Formal Total Synthesis of (-)-Brevisamide.The R3O+···H+ hydrogen bond: toward a tetracoordinate oxadionium(2+) ion.Enantioselective synthesis of tertiary α-chloro esters by non-covalent catalysisEnantioselective decarboxylative chlorination of β-ketocarboxylic acids.Extreme oxatriquinanes and a record C-O bond length.Stereoinversion of tertiary alcohols to tertiary-alkyl isonitriles and amines.SN 2 Reactions at Tertiary Carbon Centers in Epoxides.Williamson Ether Synthesis with Phenols at a Tertiary Stereogenic Carbon: Formal Enantioselective Phenoxylation of β-Keto Esters.
P2860
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P2860
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
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2010年學術文章
@zh-hant
name
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@en
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@nl
type
label
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@en
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@nl
prefLabel
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@en
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@nl
P2093
P356
P1476
1,4,7-Trimethyloxatriquinane: S(N)2 reaction at tertiary carbon.
@en
P2093
Mark Mascal
Michael D Toney
Nema Hafezi
P304
10662-10664
P356
10.1021/JA103880C
P407
P577
2010-08-01T00:00:00Z