Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

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Directing the Activation of Donor-Acceptor Cyclopropanes Towards Stereoselective 1,3-Dipolar Cycloaddition Reactions by Brønsted Base Catalysis.

P2860

Q48351526-9E4F175F-6275-4E6F-8743-A619D0A7CC23

P2860

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

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http://www.wikidata.org/entity/Q50645060

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@en

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@nl

type

Item

label

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@en

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@nl

prefLabel

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@en

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@nl

P1476

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

@en

P2093

Javier Luis-Barrera

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

Mariona Sodupe

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

Thomas Rigotti

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

Víctor Laina-Martín

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

P2860

Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.

Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions.

Visible light photoredox catalysis: applications in organic synthesis.

Intramolecular donor-acceptor cyclopropane ring-opening cyclizations.

A new golden age for donor-acceptor cyclopropanes.

Organic Photoredox Catalysis.

Enantioselective photochemistry through Lewis acid-catalyzed triplet energy transfer

Enantioselective Photocatalytic [3 + 2] Cycloadditions of Aryl Cyclopropyl Ketones.

From furan to molecular stairs: syntheses, structural properties, and theoretical investigations of oligocyclic oligoacetals.

Synthesis of [n,5]-spiroketals by ring enlargement of donor-acceptor-substituted cyclopropane derivatives.

P304

7826-7830

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P31

scholarly article

P356

10.1002/ANIE.201703334

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

P407

English

P433

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

P478

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

P50

Xavier Solans-Monfort

P577

2017-05-10T00:00:00Z

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

P698

28489267

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

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

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P2860

P2860

Visible-Light Photocatalytic Intramolecular Cyclopropane Ring Expansion.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698