A concise and flexible total synthesis of (-)-diazonamide A.
about
Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable MethodAlpha-arylation of 3-aryloxindolesNatural product synthesis at the interface of chemistry and biology.Utilizing the power of microbial genetics to bridge the gap between the promise and the application of marine natural products.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.A concise formal synthesis of diazonamide A by the stereoselective construction of the C10 quaternary centerEnantioselective TADMAP-catalyzed carboxyl migration reactions for the synthesis of stereogenic quaternary carbonTotal synthesis of atrochamins F, H, I, and J through cascade reactions.Diazonamide support studies: stereoselective formation of the C10 chiral center in both the CDEFG and AEFG fragmentsHypervalent iodine reagents in the total synthesis of natural products.Oxidative dehydrogenation of C-C and C-N bonds: A convenient approach to access diverse (dihydro)heteroaromatic compounds.An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center.External oxidant-free electrooxidative [3 + 2] annulation between phenol and indole derivatives.Synthesis of 2-oxindoles via 'transition-metal-free' intramolecular dehydrogenative coupling (IDC) of sp(2) C-H and sp(3) C-H bonds.Electrophilicity: the "dark-side" of indole chemistry.Intramolecular Larock indole synthesis: preparation of 3,4-fused tricyclic indoles and total synthesis of fargesine.Electrolytic macrocyclizations: scalable synthesis of a diazonamide-based drug development candidate.Indole Synthesis through Sequential Electrophilic N-H and C-H Bond Activation Using Iodine(III) Reactivity.Rapid assembly of spirocycles with phenol-derived biaryls with alkynes using an oxidative C-H activation/dearomatization strategy.A copper catalyzed azidation and peroxidation of β-naphthols via an oxidative dearomatization strategy.Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings.Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.
P2860
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P2860
A concise and flexible total synthesis of (-)-diazonamide A.
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
A concise and flexible total synthesis of (-)-diazonamide A.
@ast
A concise and flexible total synthesis of (-)-diazonamide A.
@en
A concise and flexible total synthesis of
@nl
type
label
A concise and flexible total synthesis of (-)-diazonamide A.
@ast
A concise and flexible total synthesis of (-)-diazonamide A.
@en
A concise and flexible total synthesis of
@nl
prefLabel
A concise and flexible total synthesis of (-)-diazonamide A.
@ast
A concise and flexible total synthesis of (-)-diazonamide A.
@en
A concise and flexible total synthesis of
@nl
P2093
P356
P1476
A concise and flexible total synthesis of (-)-diazonamide A.
@en
P2093
Anthony W G Burgett
Patrick G Harran
P304
P356
10.1002/ANIE.200352577
P407
P577
2003-10-01T00:00:00Z