(Q34261767)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

title

Asymmetric spiroacetalization catalysed by confined Brønsted acids (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

language of work or name

English

0 references

publication date

14 March 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

volume

483

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

issue

7389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

page(s)

315-319

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

cites work

Chemistry of spiroketals

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Nonanomeric spiroketals in natural products: structures, sources, and synthetic strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Catalytic asymmetric transacetalization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Chemical variation of natural product-like scaffolds: design and synthesis of spiroketal derivatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Sex-specific activity of (R)-(-)- and (S)-(+)-1,7-dioxaspiro[5.5]undecane, the major pheromone of Dacus oleae

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Rational synthesis of contra-thermodynamic spiroacetals by reductive cyclizations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Stereocontrolled synthesis of spiroketals via Ti(Oi-Pr)4-mediated kinetic spirocyclization of glycal epoxides with retention of configuration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

A novel catalytic and highly enantioselective approach for the synthesis of optically active carbohydrate derivatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Small-molecule H-bond donors in asymmetric catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Hydrogen bonding: single enantiomers from a chiral-alcohol catalyst.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Organocatalysis in a synthetic receptor with an inwardly directed carboxylic acid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Enzymelike catalysis of the Nazarov cyclization by supramolecular encapsulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

SPINOL-Derived Phosphoric Acids: Synthesis and Application in Enantioselective Friedel−Crafts Reaction of Indoles with Imines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Asymmetric additions to dienes catalysed by a dithiophosphoric acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

A powerful chiral counterion strategy for asymmetric transition metal catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

Kinetic resolution of homoaldols via catalytic asymmetric transacetalization

21 January 2018

1 reference

12 December 2020

N-phosphinyl phosphoramide--a chiral Brønsted acid motif for the direct asymmetric N,O-acetalization of aldehydes

1 reference

12 December 2020

Design of chiral N-triflyl phosphoramide as a strong chiral Brønsted acid and its application to asymmetric Diels-Alder reaction

1 reference

12 December 2020

Chiral counteranions in asymmetric transition-metal catalysis: highly enantioselective Pd/Brønsted acid-catalyzed direct alpha-allylation of aldehydes

1 reference

12 December 2020

Asymmetric counteranion-directed catalysis

1 reference

12 December 2020

Brønsted Acid catalyzed enantioselective semipinacol rearrangement for the synthesis of chiral spiroethers

1 reference

12 December 2020

Stronger Brønsted acids

1 reference

12 December 2020

Rubromycins: Structurally Intriguing, Biologically Valuable, Synthetically Challenging Antitumour Antibiotics

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10932

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NATURE10932

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

26 January 2020

1034186650

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22422266%20AND%20SRC:MED&resulttype=core&format=json