Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis. - Wikidata - wikimedia - TriplyDB

Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis.

Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis.

http://www.wikidata.org/entity/Q41910817

about

Bioinspired iterative synthesis of polyketides Chemoselective oxidation of aryl organoboron systems enabled by boronic acid-selective phase transfer 1,2-boryl migration empowers regiodivergent synthesis of borylated furans.Oxidative Heck Reactions using Aryltrifluoroborates and Aryl N-Methyliminodiacetic Acid (MIDA) Boronates Tandem Cycloisomerization/Suzuki Coupling of Arylethynyl MIDA Boronates Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studies Protecting group-free, selective cross-coupling of alkyltrifluoroborates with borylated aryl bromides via photoredox/nickel dual catalysis.Amphotericin primarily kills yeast by simply binding ergosterol.From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks.Stereoselective synthesis of dienyl-carboxylate building blocks: formal synthesis of inthomycin C.The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho-Acyloxylation and ortho-Halogenation Reactions of Arenes.A Divalent Protecting Group for Benzoxaboroles.Transitioning organic synthesis from organic solvents to water. What's your E Factor?Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks.Transforming Suzuki-Miyaura cross-couplings of MIDA boronates into a green technology: no organic solvents.Chemoselective boronic ester synthesis by controlled speciation.3-Cyanoallyl boronates are versatile building blocks in the synthesis of polysubstituted thiophenes.Total synthesis of synechoxanthin through iterative cross-coupling.Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction.Synthesis of many different types of organic small molecules using one automated process.(Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.Gold-catalyzed oxidative coupling reactions with aryltrimethylsilanes.A General Protocol for the Polycondensation of Thienyl N-Methyliminodiacetic Acid Boronate Esters To Form High Molecular Weight Copolymers.General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates.A simple and general platform for generating stereochemically complex polyene frameworks by iterative cross-coupling.C(sp3)-C(sp2) cross-coupling of alkylsilicates with borylated aryl bromides - an iterative platform to alkylated aryl- and heteroaryl boronates A general solution for the 2-pyridyl problem.Use of N-methyliminodiacetic acid boronate esters in suzuki-miyaura cross-coupling polymerizations of triarylamine and fluorene monomers.Facile synthesis of borofragments and their evaluation in activity-based protein profiling.The Molecular Industrial Revolution: Automated Synthesis of Small Molecules.Direct catalytic cross-coupling of alkenyllithium compounds.

P2860

Q27006546-F0B417CC-ACA7-427D-964A-67B7DA97F03F Q33749691-12CCE803-1E7D-4C25-B86F-7581E11748AE Q34282718-9AD70E91-1973-4DFD-AA4F-8515F5164862 Q35097896-7803D255-CD48-47E0-853E-A97FD27A8986 Q35101217-D4EEACF9-64ED-4A24-952E-B5E4F6EC3D29 Q35562633-3B2AD23D-309F-4495-BD52-0419B3BEA375 Q35775577-E92314F1-D1EE-4375-BFCE-FBA8317F1EF9 Q35787100-5554DAAB-A652-4391-8D04-0042EDF9D9AF Q36396226-9423896F-2267-4252-B4B4-FBF203EDAFB6 Q37085559-B21A5DB6-378D-423C-9565-3616D29E0847 Q37400739-10F4C391-6F90-4693-9C84-24042B186BD9 Q37542650-F18BD299-76D2-4D43-8782-6908864CA0A6 Q38244526-1EDFF305-C05D-40DD-8289-41B81AF7855D Q38273207-A7B95481-80EF-4FFF-96ED-05E3BD882332 Q39576854-26F12D4C-8DF9-4DB0-A80E-5CEDCEF9D1FF Q41484594-5D790ECF-D442-4DBB-8CFA-47CD0BE8F39B Q41528035-221F724F-7648-4EB7-A13E-4CDE8BE24BF2 Q41855490-16A56DC5-DDDC-43FD-A0A6-81282DBC4488 Q41883693-27E23ADC-1A0A-4B22-81AA-0B2E939746F9 Q41889002-1658EDBE-CD80-48D8-842F-5CEA0A18792A Q42058902-F9D33E4A-4F37-4959-AAD8-0332AC5A39BC Q42061004-83483715-107D-48DF-822A-FEBEC51933B3 Q42085799-3365F440-5203-4B7C-B80C-C814B3949A7F Q42095182-D4F7FC07-DBF4-4233-97EC-A2C1A67CE33A Q42250553-C0E64FDD-8D8D-4C59-BC7A-F222C825A65B Q42316230-1B464F79-E016-499B-8DFD-1086C935C878 Q42322782-56C1C20A-D5D1-4BAC-A085-45AE9D382B4A Q42359406-D4B328B6-C842-4994-9E1E-09CE96195C5E Q43148837-681D5107-C086-4425-B1B5-EE8F86787A7B Q50420538-FB6FDC1B-1C02-4400-B52B-F5D623FED597 Q55002332-929F57C4-28F3-4E3E-B56A-E391A79686A1

P2860

Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis.

http://www.wikidata.org/entity/Q41910817

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

2009年论文

@zh

2009年论文

@zh-cn

name

Iterative Cross-Couplng with M ...... for Small Molecule Synthesis.

@en

type

label

Iterative Cross-Couplng with M ...... for Small Molecule Synthesis.

@en

prefLabel

Iterative Cross-Couplng with M ...... for Small Molecule Synthesis.

@en

P1433

Q41910817-BE259358-05D7-4C64-A4E3-8456EC418E2D

P1476

Q41910817-5C1C085A-D28B-4DED-A48C-DC7B091BD47F

P2093

Q41910817-0655C2E7-9B3E-4E7D-9D2D-2ABA5DC572E4

Q41910817-3C777200-8D0D-4B46-949E-F8EEE26DFD99

P2860

Q41910817-00E71E81-5DB4-4B6B-836A-826F20DFA679

Q41910817-03BA4ED4-47EC-417F-8D9E-1EAEBA83B633

Q41910817-2AE7408D-8057-4CF7-A693-BB759E3DBE3E

Q41910817-3C780505-5A84-4690-8F05-CD548A0CCB4F

Q41910817-410B96D6-60F0-461B-BCC4-827AFBFBC341

Q41910817-44BE3A7D-8854-4E33-8BC5-128DA380B092

Q41910817-49D803D0-B470-4164-9CA5-026C3CE7D9F7

Q41910817-53310199-F1F2-4443-ABF3-5DF562B56FC5

Q41910817-5581AA91-2261-4C3C-8A1B-A91719466ABF

Q41910817-5A9DE5CB-370D-4BE5-A26D-FD7E934ACF32

P304

Q41910817-AC092673-1052-4E72-AD98-FFE6995E30E5

P31

Q41910817-1ADCD8C1-8477-4876-845A-33164EEC956F

P433

Q41910817-C9369E54-4BE4-40D4-9622-ADD3D614B05B

P478

Q41910817-C23D7BC7-6C91-44AE-BCD1-3EFD066C2823

P577

Q41910817-9B535251-9D34-41D7-B67D-F6EC93F8766C

P698

Q41910817-E7D0B401-48FF-4E9B-991B-72C7CEC4E54F

P932

Q41910817-19298B4F-7F04-4DAC-8CA3-5B08FF873BD4

P1433

Aldrichimica Acta

P1476

Iterative Cross-Couplng with M ...... for Small Molecule Synthesis.

@en

P2093

Eric P Gillis

http://www.w3.org/2001/XMLSchema#string

Martin D Burke

http://www.w3.org/2001/XMLSchema#string

P2860

Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling

Tandem Stille/Suzuki-Miyaura coupling of a hetero-bis-metalated diene. Rapid, one-pot assembly of polyene systems

Synthesis of four isomers of parinaric acid

Total synthesis of 2'-O-methylmyxalamide D and (6E)-2'-O-methylmyxalamide D

New Method to Prepare N-t-Butoxycarbonyl Derivatives and the Corresponding Sulfur Analogs from di-t-Butyl Dicarbonate or di-t-Butyl Dithiol Dicarbonates and Amino Acids

Universal solid-phase approach for the immobilization, derivatization, and resin-to-resin transfer reactions of boronic acids.

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

Automated solid-phase synthesis of oligosaccharides.

Alkylboranes in the Suzuki-Miyaura Coupling: Stereochemical and Mechanistic Studies.

Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure.

P304

17-27

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

42

http://www.w3.org/2001/XMLSchema#string

P577

2009-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

22523433

http://www.w3.org/2001/XMLSchema#string

P932

3328809

http://www.w3.org/2001/XMLSchema#string