Synthesis of C-glycoside analogues of α-galactosylceramide via linear allylic C-H oxidation and allyl cyanate to isocyanate rearrangement.
about
C-Glycosphingolipids with an exo-methylene substituent: stereocontrolled synthesis and immunostimulation of mouse and human natural killer T lymphocytes.C-glycosphingolipid precursors via iodocyclization of homoallyic trichloroacetimidates.Intramolecular nitrogen delivery for the synthesis of C-glycosphingolipids. Application to the C-glycoside of the immunostimulant KRN7000Synthesis and biological activities of C-glycosides of KRN 7000 with novel ceramide residues.Synthesis of C6''-modified α-C-GalCer analogues as mouse and human iNKT cell agonists.Oxidation of Hindered Allylic C–H Bonds with Applications to the Functionalization of Complex Molecules.Recent applications of Cp2TiCl in natural product synthesis
P2860
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P2860
Synthesis of C-glycoside analogues of α-galactosylceramide via linear allylic C-H oxidation and allyl cyanate to isocyanate rearrangement.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
@zh-hk
2012年論文
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2012年論文
@zh-tw
2012年论文
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2012年论文
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2012年论文
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name
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@ast
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@en
type
label
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@ast
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@en
prefLabel
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@ast
Synthesis of C-glycoside analo ...... e to isocyanate rearrangement.
@en
P2860
P356
P1433
P1476
Synthesis of C-glycoside analo ...... te to isocyanate rearrangement
@en
P2093
Robert Bittman
P2860
P304
P356
10.1021/OL2032448
P407
P50
P577
2012-01-10T00:00:00Z