Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement.

about

Catalytic Enantioselective [2,3]-Rearrangements of Allylic Ammonium Ylides: A Mechanistic and Computational Study.Pursuit of Noncovalent Interactions for Strategic Site-Selective Catalysis Incorporation of redox-inactive cations promotes iron catalyzed aerobic C-H oxidation at mild potentials.

P2860

Q37731437-234543F4-91DB-4458-83DD-8BF1D215FCAD Q42378791-A57DABC9-8423-4DD3-9F23-9868681A0620 Q55097774-23B73E54-3E56-4B98-8695-847A33FA7B3A

P2860

Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement.

Item

http://www.wikidata.org/entity/Q41873092

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Synergistic Ion-Binding Cataly ...... ic [2,3]-Wittig Rearrangement.

@en

type

Item

label

Synergistic Ion-Binding Cataly ...... ic [2,3]-Wittig Rearrangement.

@en

prefLabel

Synergistic Ion-Binding Cataly ...... ic [2,3]-Wittig Rearrangement.

@en

P1476

Synergistic Ion-Binding Cataly ...... ic [2,3]-Wittig Rearrangement.

@en

P2093

Eric N Jacobsen

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

Jennifer A Guidera

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

P2860

Attractive noncovalent interactions in asymmetric catalysis: links between enzymes and small molecule catalysts

The Cation- Box Is a Specific Phosphatidylcholine Membrane Targeting Motif

Predicting hydrogen-bond strengths from acid-base molecular properties. The pK(a) slide rule: toward the solution of a long-lasting problem.

Transition-state charge stabilization through multiple non-covalent interactions in the guanidinium-catalyzed enantioselective Claisen rearrangement

Enantioselective Claisen rearrangements with a hydrogen-bond donor catalyst.

Mechanism of amido-thiourea catalyzed enantioselective imine hydrocyanation: transition state stabilization via multiple non-covalent interactions.

Reaction progress kinetic analysis: a powerful methodology for mechanistic studies of complex catalytic reactions.

Cation-π interactions: computational analyses of the aromatic box motif and the fluorination strategy for experimental evaluation

Recent advances in asymmetric phase-transfer catalysis.

Cation-pi interactions in aromatics of biological and medicinal interest: electrostatic potential surfaces as a useful qualitative guide.

P304

416-423

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

P31

scholarly article

P356

10.1021/ACSCENTSCI.6B00125

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

P433

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

P478

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

P50

C Rose Kennedy

P577

2016-06-14T00:00:00Z

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

P698

27413786

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

P921

enantioselectivity

P932

4919771

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

Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement.

about

P2860

P2860

Synergistic Ion-Binding Catalysis Demonstrated via an Enantioselective, Catalytic [2,3]-Wittig Rearrangement.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932