Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions. - Wikidata - awgldk - TriplyDB

Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions.

Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions.

http://www.wikidata.org/entity/Q37118918

about

Catalytic asymmetric synthesis of CF3-substituted tertiary propargylic alcohols via direct aldol reaction of α-N3 amide Practical and Broadly Applicable Catalytic Enantioselective Additions of Allyl-B(pin) Compounds to Ketones and α-Ketoesters.Stereospecific Allylic Functionalization: The Reactions of Allylboronate Complexes with Electrophiles.Dynamic Cross-Exchange in Halophosphonium Species: Direct Observation of Stereochemical Inversion in the Course of an SN 2 Process.Theoretical Study on the Conformational Bioeffect of the Fluorination of Acetylcholine.A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes.Practical, Broadly Applicable, α-Selective, Z-Selective, Diastereoselective, and Enantioselective Addition of Allylboron Compounds to Mono-, Di-, Tri-, and Polyfluoroalkyl Ketones.Electronically Activated Organoboron Catalysts for Enantioselective Propargyl Addition to Trifluoromethyl Ketones.Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.

P2860

Q41919518-82C0B53C-743D-4EDC-9528-6BD3C6E78403 Q42370910-0305BCD6-E39D-48AD-9B5E-0E558ACC5813 Q44238692-1BA42482-B7A9-4B2E-ADBC-9BE53D7497E3 Q46259472-F2936498-15CF-4DCF-94E6-840CB8FA811E Q47898057-928BD894-4F5E-4A02-BB08-74B1D087D4FE Q48153508-FF565A3B-185D-4AE7-9B25-7724B8853C9B Q48225582-66FB4F41-53B5-4344-B8E8-CA4640344E3A Q48353545-94ADE73D-BF8E-4EF9-ABEF-A372BD3DABE8 Q55097774-422DD0AD-875C-47DC-AF8D-13E56EE7BF8A

P2860

Catalytic enantioselective addition of organoboron reagents to fluoroketones controlled by electrostatic interactions.

http://www.wikidata.org/entity/Q37118918

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 23 May 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Catalytic enantioselective add ...... by electrostatic interactions.

@en

Catalytic enantioselective add ...... by electrostatic interactions.

@nl

type

label

Catalytic enantioselective add ...... by electrostatic interactions.

@en

Catalytic enantioselective add ...... by electrostatic interactions.

@nl

prefLabel

Catalytic enantioselective add ...... by electrostatic interactions.

@en

Catalytic enantioselective add ...... by electrostatic interactions.

@nl

P1433

Q37118918-B4C9887A-3192-4F54-B868-AEB4702E558B

P1476

Q37118918-2B83C038-3754-40D3-A8A9-D9987241D90E

P2093

Q37118918-3DB956C8-D9EE-4ECA-BB61-83F2B3165947

Q37118918-610A4081-6103-4B77-8C10-E8413DA388CB

Q37118918-67F403D6-191E-4DCC-9E7A-804854E14AC1

Q37118918-703239A3-F52B-4D56-AC82-1C71800A99AA

Q37118918-71791364-3721-44E3-833E-E0F9868C5782

Q37118918-ABC20B8E-858F-4BE3-8BC5-5049E0BDF6CE

P2860

Q37118918-0357018D-91C3-474E-9206-47ACD118FC8D

Q37118918-10D8E6A7-7A8A-4A20-998B-43DA0F32BAA9

Q37118918-12BA8C56-CEDD-4E35-82C9-E122F489A018

Q37118918-1964D18B-C12D-4204-A8E2-C0F75A9486A3

Q37118918-1DDA7E03-C497-4847-891B-00046759CE5C

Q37118918-3705D988-CA34-4FCB-ADB9-CB8D6B1A844A

Q37118918-375F0459-7434-4368-888F-165491C16552

Q37118918-3766FA3C-AB03-4171-BBB9-44635876F4B9

Q37118918-3A2C4B3A-7256-4060-86A0-A83DF2ADF669

Q37118918-3FEF5269-B918-4ED9-B223-F60579E7FF73

P2888

Q37118918-85489708-C9ED-49B6-B889-54FDAEF1E7AE

P304

Q37118918-2675497C-68E6-4077-8FB2-E92A8BEFFD7A

P31

Q37118918-7A38A7F6-40F2-47F1-9F86-4D484D9C1716

P356

Q37118918-1575BEB4-A5D2-41C6-9F73-D6577DB2454C

P433

Q37118918-65C04057-9352-4C8E-9DA1-C8F560E2D15A

P478

Q37118918-8E7C1CDA-0EC0-4305-8BE6-0E64E572CCC0

P50

Q37118918-5872F3E1-896B-4143-9149-0589A3A0F44D

P577

Q37118918-E8C92610-8359-479A-BA20-7FA26661E715

P698

Q37118918-571F5785-A097-4701-B3BA-BB8A0311867F

P921

Q37118918-877C0CDA-F52A-4F11-9329-0AD01223F4E7

P932

Q37118918-628E9F5B-B792-417B-80B1-D11E61843198

P356

P1433

Nature Chemistry

P1476

Catalytic enantioselective add ...... by electrostatic interactions.

@en

P2093

Daniel L Silverio

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

Daniel W Robbins

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

Farid W van der Mei

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

Fredrik Haeffner

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

KyungA Lee

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

Sebastian Torker

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

P2860

Understanding organofluorine chemistry. An introduction to the C-F bond

Organic Fluorine Hardly Ever Accepts Hydrogen Bonds

Quantum mechanical investigation of the effect of catalyst fluorination in the intermolecular asymmetric Stetter reaction.

Organic fluorine: odd man out.

Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols

An efficient, practical, and enantioselective method for synthesis of homoallenylamides catalyzed by an aminoalcohol-derived, boron-based catalyst

Organic fluorine compounds: a great opportunity for enhanced materials properties.

Fluorine conformational effects in organocatalysis: an emerging strategy for molecular design.

The influence of fluorine in asymmetric catalysis.

Applications of Fluorine in Medicinal Chemistry.

P2888

P304

768-777

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

P31

scholarly article

P356

10.1038/NCHEM.2523

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

P433

8

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

P478

8

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

P50

Amir H. Hoveyda

P577

2016-05-23T00:00:00Z

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

P698

27442282

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

P921

enantioselectivity

P932

4957664

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