about
Approach toward the total synthesis of 5-hydroxyaloin AFacile Access to Sterically Hindered Aryl Ketones via Carbonylative Cross-Coupling: Application to the Total Synthesis of Luteolin.Studies Toward the Syntheses of Pluramycin Natural Products. The First Total Synthesis of Isokidamycin.Tandem Electrocyclic Ring Opening/Radical Cyclization: Application to the Total Synthesis of Cribrostatin 6Natural Products and Their Mimics as Targets of Opportunity for Discovery.Regioselective synthesis of naphthoquinone/naphthoquinol-carbohydrate hybrids by [4 + 2] anionic annulations and studies on their cytotoxicity.Studies toward the total synthesis of pluraflavin ANeoadenoloside A, a highly functionalized diterpene C-glycoside, from Isodon adenolomus.Ruthenium(0)-Catalyzed [4+2] Cycloaddition of Acetylenic Aldehydes with α-Ketols: Convergent Construction of Angucycline Ring Systems.Ruthenium(0) Catalyzed Endiyne-α-Ketol [4 + 2] Cycloaddition: Convergent Assembly of Type II Polyketide Substructures via C-C Bond Forming Transfer HydrogenationPhotoassisted diversity-oriented synthesis: accessing 2,6-epoxyazocane (oxamorphan) cores.Halogenation effects in intramolecular furan Diels-Alder reactions: broad scope synthetic and computational studies.Synthesis of the pluramycins 2: total synthesis and structure assignment of saptomycin B.Ready access to 3-amino-2,3-dideoxysugars via regio- and stereo-selective tandem hydroamination-glycosylation of glycals.Unusual structure-energy correlations in intramolecular Diels-Alder reaction transition states.Synthesis of the pluramycins 1: two designed anthrones as enabling platforms for flexible bis-C-glycosylation.
P2860
Q34423795-5C49E25D-FE3D-4F7B-9FC7-DB7EB3CE659CQ35067332-A611D4F6-8920-4D96-AEFB-274176B5F6FEQ35133009-81EE86CE-CB92-4E48-92B9-412622AFD0C0Q35573037-9EFF851F-4E5A-4D35-9B56-87CF17C4ABCCQ38557129-C21E9FC2-E2F4-4FF2-866E-A130791CBCEAQ38736749-84235366-3150-4683-BC87-C255831BED8BQ39077644-D6C7CDAA-6D77-49AE-A4AD-CC9BFBD0A908Q39323322-3424E4B8-E873-4A18-8A0D-B251670C8569Q41875924-F90500B8-3DA1-4CCF-98FB-873847AE4496Q41878135-5FB2C292-8A0A-49C5-866F-9B06C6A6CB7BQ43026779-BF7B3932-77DE-497A-ADE1-08D568576961Q43792364-937EF0C6-114F-4F0B-832D-4CF30E00A8A1Q45705768-255926E9-9036-4ADF-987D-15D037E359CAQ51583684-664394D8-24FA-405A-A7D0-A01106143F71Q53429488-3DF12B7F-278A-4C86-BF9D-28AA06572A57Q54388241-50A52E27-5D25-4E40-A1D3-5C0436CE2C50
P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Total synthesis of isokidamycin.
@ast
Total synthesis of isokidamycin.
@en
Total synthesis of isokidamycin.
@nl
type
label
Total synthesis of isokidamycin.
@ast
Total synthesis of isokidamycin.
@en
Total synthesis of isokidamycin.
@nl
prefLabel
Total synthesis of isokidamycin.
@ast
Total synthesis of isokidamycin.
@en
Total synthesis of isokidamycin.
@nl
P2093
P2860
P356
P1476
Total synthesis of isokidamycin.
@en
P2093
B Michael O'Keefe
David E Kaelin
Douglas M Mans
Stephen F Martin
P2860
P304
15528-15530
P356
10.1021/JA107926F
P407
P577
2010-11-01T00:00:00Z