About: Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically

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About: Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically Goto Sponge NotDistinct Permalink

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scholarly article by Forrest K. Sheffy et al published August 1984 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1984 (uk) article scientifique publié en 1984 (fr) im August 1984 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Forrest K. Sheffy et al published August 1984 in Journal of the American Chemical Society (en)
publication date	wds:Q56482567-EC9AC14D-FB7D-4AAB-AB88-AA742D911AF7
publication date	1984-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56482567-DFE6BFA1-10F7-45C2-B845-1985FD8CCCDD
language of work or name	English
author name string	wds:Q56482567-2371C718-8AE3-4103-8924-1BFEA45ABF59 wds:Q56482567-3FA41D04-23AC-4E0C-A10C-EB89C1735982 wds:Q56482567-B57C8FAE-7501-475E-9667-2AC689520A3F
author name string	Forrest K. Sheffy J. K. Stille J. P. Godschalx
rdfs:label	Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (en) Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (nl)
skos:prefLabel	Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (en) Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (nl)
name	Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (en) Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (nl)
title	wds:Q56482567-4C97F8B1-F220-4C57-A924-6F350275210F
title	Palladium-catalyzed cross coupling of allyl halides with organotin reagents: a method of joining highly functionalized partners regioselectively and stereospecifically (en)
page(s)	wds:Q56482567-6F744D75-EE32-4F60-8B7F-9CFDB5955DA6
page(s)	4833-4840
instance of	wds:Q56482567-8D4D52F5-A67B-4CF5-AC9A-0151E4F6C1C5
instance of	scholarly article
main subject	wds:Q56482567-71A1E98D-F64D-4395-9E5D-A1307BF6908D wds:Q56482567-C41D1355-822A-46B4-8999-CB687C85C8D8
main subject	palladium organotin chemistry
published in	wds:Q56482567-9574872D-381A-4588-8A61-2A2FFDFE6035
published in	Journal of the American Chemical Society
issue	wds:Q56482567-0AEDED45-E2BD-4154-9F65-E61FC731E801
volume	wds:Q56482567-A6FC3DB9-F759-4B9D-B0B6-E711B89592FE
issue	17
volume	106
DOI	wds:Q56482567-40D5E847-088F-4B61-BE4C-6F0A70572076
DOI	http://dx.doi.org/10.1021/JA00329A032
DOI	10.1021/JA00329A032
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56482567
is cites work of	Palladium-catalyzed 1,1-difunctionalization of ethylene New insights into the mechanism of palladium-catalyzed allylic amination The biosynthesis of ubiquinone: Synthesis and enzymatic modification of biosynthetic precursors Pd-catalyzed carbonylative cross-coupling reactions by triorganoindiums: highly efficient transfer of organic groups attached to indium under atmospheric pressure Chemical and biological studies of nakiterpiosin and nakiterpiosinone Marine cytotoxic macrolides haterumalides and biselides, and related natural products Total synthesis of (+)-dactylolide through an efficient sequential Peterson olefination and Prins cyclization reaction Palladium-catalyzed carbonylation reactions of aryl halides and related compounds 2-furyl phosphines as ligands for transition-metal-mediated organic synthesis The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation Mechanistic investigation of the nickel-catalyzed Suzuki reaction of N,O-acetals: evidence for boronic acid assisted oxidative addition and an iminium activation pathway Synthesis of quaternary amino acids bearing a (2'Z)-fluorovinyl alpha-branch: potential PLP enzyme inactivators. Synthesis of ent-Haterumalide NA (ent-Oocydin A) Methyl Ester Stereocontrolled Synthesis of Quaternary β,γ-Unsaturated Amino Acids: Chain Extension of D- & L- α-(2-Tributylstannyl)Vinyl Amino Acids. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies A formal [3,3]-sigmatropic rearrangement route to quaternary alpha-vinyl amino acids: use of allylic N-PMP trifluoroacetimidates Total Synthesis of (-)-Nodulisporic Acid D. Regio- and stereoselective allylic trifluoromethylation and fluorination using CuCF3 and CuF reagents. Progress in hydroformylation and carbonylation Regioselective syntheses of substituted furans Cross-Coupling of Aryl Halides and Allyl Acetates with Arylboron Reagents in Water Using an Amphiphilic Resin-Supported Palladium Catalyst Total synthesis of architecturally complex indole terpenoids: strategic and tactical evolution. Highly selective intermolecular Heck reaction for the soluble polymer supported synthesis of glutamic acid analogues Intermolecular metallo-ene reaction catalyzed by palladium Efficient ruthenium carbenoid-catalyzed cross-metathesis of allyl halides with olefins Synthesis of alpha- and beta-C-Aryl Delta(2)-Glycopyranosides from p-tert-Butylphenyl Delta(2)-Glycopyranosides via Grignard Reagents Palladium complex catalyzed acylation of allylic esters with acylsilanes Palladium-Catalyzed Carbonylative Transformation of C(sp3)–X Bonds Nickel-catalyzed allylic carbonylative coupling of alkyl zinc reagents with tert-butyl isocyanide Palladium-catalyzed cross-coupling reactions of allylic halides and acetates with indium organometallics Palladium-catalyzed hydroarylation of 1,3-dienes with boronic esters via reductive formation of pi-allyl palladium intermediates under oxidative conditions Palladium Catalyzed Regioselective β-Acetonation−α-Allylation of Activated Olefins in One Shot Palladium(0)-catalyzed direct cross-coupling reaction of allylic alcohols with aryl- and alkenylboronic acids The Stille Reaction A straightforward and versatile synthetic approach to 1-azabicyclic alkaloids Synthesis of low-generation, aryl-/alkyl-type, nonpolar dendrons carrying protected hydroxyalkyl groups in the periphery The Aliphatic Friedel–Crafts Reaction Palladium-catalyzed carbonylative coupling of aryl iodides with an organocopper reagent: a straightforward procedure for the synthesis of aryl trifluoromethyl ketones Palladium(0)-Catalyzed Allylation of Highly Acidic and Nonnucleophilic Anilines. The Origin of Stereochemical Scrambling When Using Allylic Carbonates Simple and efficient nickel-catalyzed cross-coupling reaction of alkynylalanes with benzylic and aryl bromides Rhodium-catalyzed cross-coupling of allyl alcohols with aryl- and vinylboronic acids in ionic liquids Nickel-catalyzed reductive allylation of aryl bromides with allylic acetates A new method for installation of aryl and alkenyl groups onto a cyclopentene ring and synthesis of prostaglandins Total Synthesis of (-)-Nodulisporic Acids D, C, and B: Evolution of a Unified Synthetic Strategy Carbostannolysis Mediated by Bis(pentamethylcyclopentadienyl)lanthanide Catalysts. Utility in Accessing Organotin Synthons Palladium(0)-catalyzed allylation of highly acidic and non-nucleophilic arenesulfonamides, sulfamide, and cyanamide. I Bis(dibenzylideneacetone)palladium(0) Suzuki–Miyaura coupling of phosphinoyl-α-allenic alcohols with arylboronic acids catalyzed by a palladium complex “on water”: an efficient method to generate phosphinoyl 1,3-butadienes and derivatives Comparative effects of conjugated and deconjugated isomeric enones on the transannular Diels-Alder reaction Radical Transformations towards the Synthesis of Quinoline: A review [Development of unprotected syntheses in aqueous media] Direct Pd-catalyzed cross-coupling of functionalized organoaluminum reagents
is cites work of	wds:Q33584817-384EC91F-EEDF-44EA-875C-C0D92621E317 wds:Q36896576-B17EF9F3-9D87-478D-B419-21776B2208EA wds:Q50277018-134A7755-B854-4448-8033-FFA37C652944 wds:Q58103662-3E9401ED-8712-48A5-8A19-E418DEEC7EDA wds:Q74151998-E0817CBC-B23E-4F08-87A1-57BA5F405408 wds:Q74837510-BCFCC36B-8EBE-4701-B32F-DE8A23C064FD

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