Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
about
Total synthesis of (±)-rocaglamide via oxidation-initiated Nazarov cyclization.The chemistry of bisallenes.Asymmetric synthesis of 2-substituted oxetan-3-ones via metalated SAMP/RAMP hydrazones.Direct entry to erythronolides via a cyclic bis[allene].Spirodiepoxide-based cascades: direct access to diverse motifs.Desmethyl Macrolides: Synthesis and Evaluation of 4,8-Didesmethyl TelithromycinDesmethyl Macrolides: Synthesis and Evaluation of 4,10-Didesmethyl Telithromycin.Spirodiepoxides: synthesis of epoxomicinoids.Modular functionalization of allenes to aminated stereotriadsSpirodiepoxide strategy to the C ring of pectenotoxin 4: synthesis of the C1-C19 sector.Toward an integrated route to the vernonia allenes and related sesquiterpenoids.Cadmium iodide-mediated allenylation of terminal alkynes with ketones.The conversion of allenes to strained three-membered heterocycles.
P2860
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P2860
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@en
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@nl
type
label
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@en
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@nl
prefLabel
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@en
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@nl
P2093
P2860
P356
P1433
P1476
Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A.
@en
P2093
Lawrence J Williams
Partha Ghosh
Thomas J Emge
P2860
P304
P356
10.1021/OL901755A
P407
P577
2009-10-01T00:00:00Z