(Q46360686)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18800380%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

Enantioselective catalytic reduction of ketoimines with trichlorosilane promoted by readily available chiral Lewis bases (English)

1 reference

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14 January 2020

1 reference

1 reference

2

1 reference

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14 January 2020

Franco Cozzi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18800380%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Sergio Rossi

4

1 reference

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14 January 2020

author name string

Stefania Guizzetti

1

1 reference

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14 January 2020

Giuseppe Celentano

5

1 reference

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14 January 2020

publication date

1 January 2009

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14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18800380%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

volume

21

1 reference

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14 January 2020

issue

1

1 reference

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14 January 2020

page(s)

233-238

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18800380%20AND%20SRC:MED&resulttype=core&format=json

Additions of Organometallic Reagents to C=N Bonds: Reactivity and Selectivity

14 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

From a chiral switch to a ligand portfolio for asymmetric catalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

In the Golden Age of Organocatalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Enantioselective organocatalytic transfer hydrogenation reactions using Hantzsch esters

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Asymmetric organocatalytic reductions mediated by dihydropyridines.

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Role of noncovalent interactions in the enantioselective reduction of aromatic ketimines with trichlorosilane

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

l-Piperazine-2-carboxylic acid derived N-formamide as a highly enantioselective Lewis basic catalyst for hydrosilylation of N-aryl imines with an unprecedented substrate profile

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

A highly enantioselective lewis basic organocatalyst for reduction of N-aryl imines with unprecedented substrate spectrum

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Remote chiral induction in the organocatalytic hydrosilylation of aromatic ketones and ketimines

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

S-chiral sulfinamides as highly enantioselective organocatalysts

1 reference

https://api.crossref.org/works/10.1002%2FCHIR.20615

7 January 2021

Identifiers

DOI

10.1002/CHIR.20615

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18800380%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference