About: Redox economy in organic synthesis

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scientific article published on January 2009

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2009 (ast) наукова стаття, опублікована в січні 2009 (uk) مقالة علمية نشرت في يناير 2009 (ar) scientific article published on January 2009 (en)
publication date	wds:Q37417218-AD3CBECF-10F4-44B7-9A5A-0C7440D44D1A
publication date	2009-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37417218-7FF3F27D-B1FA-48D2-86E3-3A2A3A89EA0D
language of work or name	English
cites work	wds:Q37417218-C23C1876-78FE-4BB0-BC25-15B70E377ED4
cites work	LXIII.—A synthesis of tropinone
author name string	wds:Q37417218-7040EFC1-6007-479F-9A8F-387AB6BF7605 wds:Q37417218-AC731EA5-492F-4247-A32C-5E00594DA456 wds:Q37417218-C5711224-40B5-4772-BF91-1D2D5F522210
author name string	Phil S Baran Reinhard W Hoffmann Noah Z Burns
rdfs:label	Redox economy in organic synthesis (en) Redox economy in organic synthesis (nl) Redox economy in organic synthesis (ast)
skos:prefLabel	Redox economy in organic synthesis (en) Redox economy in organic synthesis (nl) Redox economy in organic synthesis (ast)
name	Redox economy in organic synthesis (en) Redox economy in organic synthesis (nl) Redox economy in organic synthesis (ast)
title	wds:Q37417218-87DB15BF-C827-4328-AE02-2636BBE7539A
title	Redox economy in organic synthesis (en)
page(s)	wds:Q37417218-E6D31AC3-68ED-4B5A-A480-F08625F2B7CD
page(s)	2854-2867
instance of	wds:Q37417218-56C447C2-523F-4B61-A3C0-D34D9BCD67B7
instance of	scholarly article
PubMed ID	wds:Q37417218-80075023-6491-444E-A922-39FDF4CF0BB3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19294720
PubMed ID	19294720
published in	wds:Q37417218-57CD3636-8817-45E9-9A0C-539A84A6E0A7
published in	Angewandte Chemie International Edition
issue	wds:Q37417218-E12A216D-20BB-4368-8DE5-F5676FF4B813
volume	wds:Q37417218-4DE2A41F-8C2B-4018-BC2F-CE4E2CAC6181
issue	16
volume	48
DOI	wds:Q37417218-898B0A03-F415-40D6-AF7E-DBE46961041B
DOI	http://dx.doi.org/10.1002/ANIE.200806086
DOI	10.1002/ANIE.200806086
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37417218
is cites work of	Heterocycle Formation via Palladium-Catalyzed C-H Functionalization Hypervalent iodine reagents in the total synthesis of natural products Nature-inspired total synthesis of (-)-fusarisetin A. Fusarisetin A: Scalable Total Synthesis and Related Studies. Total synthesis of bryostatin 7 via C-C bond-forming hydrogenation Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction A flow-microreactor approach to protecting-group-free synthesis using organolithium compounds. Total synthesis of palau'amine Photochemical reactions as key steps in natural product synthesis Modular Synthesis of Novel Macrocycles Bearing α,β-Unsaturated Chemotypes through a Series of One-Pot, Sequential Protocols Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency Translating Nature's Library: The Bryostatins and Function-Oriented Synthesis Total synthesis of haouamine A: the indeno-tetrahydropyridine core Scalable synthesis of cortistatin A and related structures Chemo- and site-selective derivatizations of natural products enabling biological studies Catalytic selective synthesis Protecting-group-free synthesis as an opportunity for invention Visible-light-mediated conversion of alcohols to halides Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity 14-step synthesis of (+)-ingenol from (+)-3-carene Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon Protecting-group-free diastereoselective C-C coupling of 1,3-glycols and allyl acetate through site-selective primary alcohol dehydrogenation Direct entry to erythronolides via a cyclic bis[allene]. Palladium-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen cleavage: general strategy for amide N-C bond activation. Organocatalytic cascade reactions as a new tool in total synthesis Rewiring chemistry: algorithmic discovery and experimental validation of one-pot reactions in the network of organic chemistry. Enantioselective Heck arylations of acyclic alkenyl alcohols using a redox-relay strategy Catalytic asymmetric epoxidation of alpha-branched enals Natural product synthesis in the age of scalability A redox economical synthesis of bioactive 6,12-guaianolides. Improved synthesis of UDP-2-(2-ketopropyl)galactose and a first synthesis of UDP-2-(2-ketopropyl)glucose for the site-specific linking of biomolecules via modified glycan residues using glycosyltransferases Strained cyclophane natural products: macrocyclization at its limits Redox-neutral copper(II) carboxylate catalyzed α-alkynylation of amines Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition Catalytic Enantioselective Carbonyl Allylation and Propargylation via Alcohol-Mediated Hydrogen Transfer: Merging the Chemistry of Grignard and Sabatier Catalytic enantioselective OFF ↔ ON activation processes initiated by hydrogen transfer: concepts and challenges. Asymmetric alcohol C-H allylation and syn-crotylation: C9-C20 of tetrafibricin Diastereo- and Enantioselective Iridium Catalyzed Coupling of Vinyl Aziridines with Alcohols: Site-Selective Modification of Unprotected Diols and Synthesis of Substituted Piperidines Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes Symmetry-Driven Strategy for the Assembly of the Core Tetracycle of (+)-Ryanodine: Synthetic Utility of a Cobalt-Catalyzed Olefin Oxidation and α-Alkoxy Bridgehead Radical Reaction. Total synthesis of TK-57-164A, isariotin F, and their putative progenitor isariotin E. Is there no end to the total syntheses of strychnine? Lessons learned in strategy and tactics in total synthesis

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