Development of an enantiodivergent strategy for the total synthesis of (+)- and (-)-dragmacidin f from a single enantiomer of quinic Acid.
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Total syntheses of indolactam alkaloids (-)-indolactam V, (-)-pendolmycin, (-)-lyngbyatoxin A, and (-)-teleocidin A-2.Dragmacidin E synthesis studies. Preparation of a model heptacyclic core structure.Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation.Syntheses of Cyclic Guanidine-Containing Natural Products.An efficient deprotection of N-trimethylsilylethoxymethyl (SEM) groups from dinucleosides and dinucleotides.Total synthesis of (±)-dragmacidin EThe Neber route to substituted indolesA strategy for the total synthesis of dragmacidin E. Construction of the core ring system.Catalytic enantioselective total synthesis of (+)-eucomic acid.Total Synthesis of (±)-Dragmacidin E: Problems Solved and Lessons Learned.C-H activation: a complementary tool in the total synthesis of complex natural products.The emergence of sulfoxides as efficient ligands in transition metal catalysis.C-H Bond Functionalizations with Palladium(II): Intramolecular Oxidative Annulations of Arenes.Oxidative cyclizations in a nonpolar solvent using molecular oxygen and studies on the stereochemistry of oxypalladation10-Step Asymmetric Total Synthesis and Stereochemical Elucidation of (+)-Dragmacidin D.Catalytic enantioselective alkylation of substituted dioxanone enol ethers: ready access to Calpha-tetrasubstituted hydroxyketones, acids, and estersEnantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.Bright, Red Single-Molecule Emitters: Synthesis and Properties of Environmentally Sensitive Dicyanomethylenedihydrofuran (DCDHF) Fluorophores with Bisaromatic Conjugation.A rapid and convergent synthesis of the integrastatin core.Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.
P2860
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P2860
Development of an enantiodivergent strategy for the total synthesis of (+)- and (-)-dragmacidin f from a single enantiomer of quinic Acid.
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年學術文章
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2005年學術文章
@zh-hant
name
Development of an enantiodiver ...... gle enantiomer of quinic Acid.
@en
Development of an enantiodivergent strategy for the total synthesis of
@nl
type
label
Development of an enantiodiver ...... gle enantiomer of quinic Acid.
@en
Development of an enantiodivergent strategy for the total synthesis of
@nl
prefLabel
Development of an enantiodiver ...... gle enantiomer of quinic Acid.
@en
Development of an enantiodivergent strategy for the total synthesis of
@nl
P356
P1476
Development of an enantiodiver ...... ngle enantiomer of quinic Acid
@en
P2093
Brian M Stoltz
Neil K Garg
P304
P356
10.1021/JA050586V
P407
P577
2005-04-01T00:00:00Z