Asymmetric allylboration and ring closing alkene metathesis: a novel strategy for the synthesis of glycosphingolipids.
about
PhenyllithiumA relay ring-closing metathesis synthesis of dihydrooxasilines, precursors of (Z)-iodo olefins.Temporary silicon-tethered ring-closing metathesis: recent advances in methodology development and natural product synthesis.Asymmetric synthesis of 2 degrees- and 3 degrees-Carbinols via B-methallyl-10-(TMS and Ph)-9-borabicyclo[3.3.2]decanes.Synthesis of substituted Z-styrenes by Hiyama-type coupling of oxasilacycloalkenes: application to the synthesis of a 1-benzoxocane.Allylboration of Carbonyl Compounds
P2860
Asymmetric allylboration and ring closing alkene metathesis: a novel strategy for the synthesis of glycosphingolipids.
description
2000 nî lūn-bûn
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2000年の論文
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2000年学术文章
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2000年学术文章
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name
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@en
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@nl
type
label
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@en
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@nl
prefLabel
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@en
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@nl
P2093
P356
P1476
Asymmetric allylboration and r ...... nthesis of glycosphingolipids.
@en
P2093
P304
P356
10.1021/JO000690P
P407
P577
2000-10-01T00:00:00Z