about
Studies in the Total Synthesis of Heliquinomycinone: Proof of Concept and Assembly of a Fully Mature Spirocyclization Precursor This work was supported by the National Institutes of Health (Grant numbers: AI 16943 and HL25848). A Postdoctoral FellowBiology-oriented synthesis.A late-stage intermediate in salinomycin biosynthesis is revealed by specific mutation in the biosynthetic gene cluster.Catalytic Asymmetric Hetero-Diels-Alder Reactions of Carbonyl Compounds and Imines.Asymmetric spiroacetalization catalysed by confined Brønsted acids.Two Remarkable Epimerizations Imperative for the Success of an Asymmetric Total Synthesis of (+)-AigialospirolGold-catalyzed three-component spirocyclization: a one-pot approach to functionalized pyrazolidines.Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation.Nitroalkanes as central reagents in the synthesis of spiroketals.Chemical and enzymatic approaches to carbohydrate-derived spiroketals: di-D-fructose dianhydrides (DFAs).Asymmetric synthesis of naturally occurring spiroketals.Total synthesis of the cytotoxic cyclodepsipeptide (-)-doliculide: the "ester" effect in acyclic 1,3-induction of deoxypropionates.Generation, structure and reactivity of tertiary organolithium reagents.Cyclization of polyketides and non-ribosomal peptides on and off their assembly lines.Evidence that Cerambycid Beetles Mimic Vespid Wasps in Odor as well as Appearance.Asymmetric Synthesis of Spiroketals with Aminothiourea Catalysts.Designed Spiroketal Protein Modulation.Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of furanyl (gamma)- and pyranyl (delta)-lactols.A Pd(II)-catalyzed asymmetric approach toward chiral [3.3.1]-bicyclic ketals using 2-hydroxyphenylboronic acid as a pro-bis(nucleophile).Synthesis and DFT calculations of spirooxaphosphirane complexes.A catalytic multicomponent coupling reaction for the enantioselective synthesis of spiroacetals.Stereocontrolled Synthesis of Spiroketals: An Engine for Chemical and Biological Discovery.Metal-free diastereoselective construction of bridged ketal spirooxindoles via a Michael addition-inspired sequence.An Efficient Synthesis of Spiro[indoline-3,9'-xanthene]trione Derivatives Catalyzed by Magnesium Perchlorate.Stereoselective Synthesis of the Proposed C79-C104 Fragment of Symbiodinolide.Enantioselective Organocatalytic Cascade Approach to Different Classes of Benzofused Acetals.Synthesis of spirocyclic orthoesters by 'anomalous' rhodium(ii)-catalysed intramolecular C-H insertions.Copper(I)-catalyzed three-component reaction of terminal propargyl alcohols, aldehydes, and amines: synthesis of 3-amino-2-pyrones and 2,5-dihydrofurans.Catalytic asymmetric [3+2] cycloaddition of aromatic aldehydes with oxiranes by C-C bond cleavage of epoxides: highly efficient synthesis of chiral 1,3-dioxolanes.Heteroatom-Guided, Palladium-Catalyzed, Site-Selective C-H Arylation of 4H-Chromenes: Diastereoselective Assembly of the Core Structure of Myristinin B through Dual C-H Functionalization.In Vitro Neuroprotective and Anti-Inflammatory Activities of Natural and Semi-Synthetic Spirosteroid Analogues.Intramolecular iodoetherification of ene or diene ketals: facile synthesis of spiroketals.Catalytic asymmetric synthesis of aromatic spiroketals by spinphox/iridium(I)-catalyzed hydrogenation and spiroketalization of α,α'-bis(2-hydroxyarylidene) ketones.Phosphine-catalyzed domino reaction for the synthesis of conjugated 2,3-dihydrofurans from allenoates and Nazarov reagents.A convergent total synthesis of the telomerase inhibitor (±)-γ-rubromycin.NEW POLYETHYLENE GLYCOL POLYMERS AS KETAL PROTECTING GROUPS – A POLYMER SUPPORTED APPROACH TO SYMMETRICALLY SUBSTITUTED SPIROKETALSThe Orthoester Johnson-Claisen Rearrangement in the Synthesis of Bioactive Molecules, Natural Products, and Synthetic Intermediates - Recent AdvancesDesigned Spiroketal Protein ModulationSynthesis of spiroketals under neutral conditions via a type III ring-rearrangement metathesis strategy
P2860
Q33185001-60836B3A-C161-4685-84DB-A741F7F5E7F2Q34061956-2DF21577-48B0-40F9-B4E1-191E6C0376C4Q34072847-4CA21B76-5CB9-47F1-8854-AB84994C7186Q34089234-5A6E4E03-051F-43AA-92BB-2DB3D98D78E7Q34261767-3CCD4970-AF8C-4A73-9BE9-6C9480DFA6D7Q34473055-B0BD5246-EB10-4272-8305-200E9DC97C8CQ35874808-B0F45B72-C8D4-43F3-894E-EB150F73B06EQ36170243-5FC59F91-A6AD-4B2C-9F03-68021671A11AQ37096496-4C9F3A53-D7B2-4F54-A0BF-E37B6E268A5CQ37270367-82A334A2-A386-4CA9-B8C1-DB3CBAD6A469Q37270393-4617F5F8-F889-44F8-B54E-A340F2D879A5Q37484225-719006EB-207A-4108-86DE-E8FE0A9DAD53Q38283084-ECBB0C74-36B1-486D-95A3-1E5AFD7FC3DAQ38646975-AB39DC44-4CDE-4BA7-9349-5C87D4D72DC3Q39084953-18755AE8-141F-4633-A238-45FD508DFA1AQ40382893-08A91B03-968D-4F16-B9B4-68DB9411AC17Q42259127-D6A69BEF-6921-49D7-8D02-CEC07C725619Q44830526-856F00EA-1BBF-4FC2-97E6-97DEE1CDEB18Q44979234-61F9DF7E-045E-4B53-A21F-72B1ECB8490EQ45830772-8E82A3D6-7579-46D8-A582-24250A701738Q45896634-D2F3AD2A-F8E1-4BC9-A55E-C03947DF2AFFQ47379970-5FA1E21A-6041-484C-937B-8313352BE9F3Q47623869-A0B75A57-0B15-4DD0-B831-3728BDC5C9CAQ47833883-3E803572-101E-4CC2-812A-E3D37BEDA789Q48089863-4C8AA57D-2615-4B73-A9F9-A4F41491B5B0Q49068362-EEBCFA7B-D002-44DE-91EC-C0CC0AF7C3E6Q49849077-F2EC7E81-899F-4E60-9C2D-312AD08F2A32Q50446889-269B2AD6-102D-4420-A998-ACE8AE71337AQ50463652-DD82CCCE-0564-490C-A9D1-B3006BA6652EQ50972231-C17F4469-ADD3-43D1-897C-356E4AE83B09Q51478239-862E1228-5349-416B-A6FF-9E75B0E619B6Q52712185-CE332C67-72A9-4D21-B538-7EFC81DDE236Q52731864-C9904A2B-C2F7-4E34-819C-1752C3148C8CQ52736459-62F14B44-0E33-4D7C-9528-FAAFC6845062Q52878532-5C65E439-3DA6-44AF-A36D-A95DC067985FQ56953089-3A8EA81C-407E-4399-B74A-B061415B5BECQ57482446-9CBB380A-8836-4622-B7E2-B41B128FC712Q57531344-C8140E5D-E4AD-48BC-958B-539A048F7150Q57776819-31C2457E-4CE5-4C6A-89B8-3272ACB93344
P2860
description
1989 nî lūn-bûn
@nan
1989 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Chemistry of spiroketals
@ast
Chemistry of spiroketals
@en
type
label
Chemistry of spiroketals
@ast
Chemistry of spiroketals
@en
prefLabel
Chemistry of spiroketals
@ast
Chemistry of spiroketals
@en
P356
P1433
P1476
Chemistry of spiroketals
@en
P2093
Francoise Perron
Kim F. Albizati
P304
P356
10.1021/CR00097A015
P577
1989-11-01T00:00:00Z