An abiotic strategy for the enantioselective synthesis of erythromycin B.
about
Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.Studies toward welwitindolinones: formal syntheses of N-methylwelwitindolinone C isothiocyanate and related natural productsTotal synthesis of (-)-4,8,10-tridesmethyl telithromycin.Natural Products and Their Mimics as Targets of Opportunity for Discovery.Boron enolate chemistry toward the syntheses of polyketide stereotetrads.Total synthesis of 6-deoxyerythronolide B via C-C bond-forming transfer hydrogenationModeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.On the macrocyclization of the erythromycin core: preorganization is not required.Natural Products as Platforms To Overcome Antibiotic Resistance.
P2860
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P2860
An abiotic strategy for the enantioselective synthesis of erythromycin B.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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name
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@en
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@nl
type
label
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@en
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@nl
prefLabel
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@en
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@nl
P2093
P356
P1476
An abiotic strategy for the enantioselective synthesis of erythromycin B.
@en
P2093
Andrew S Judd
Anne Hodgson
Paul J Hergenrother
Stephen F Martin
Wen-Cherng Lee
P304
P356
10.1002/ANIE.200351136
P407
P577
2003-07-01T00:00:00Z