(Q57006756)

5

0 references

author name string

Marco Potowski

1

0 references

Markus Schürmann

2

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Hans Preut

3

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publication date

18 March 2012

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number of pages

3

1 reference

https://scigraph.springernature.com/pub.10.1038/nchembio.901

inferred from page(s)

published in

Nature Chemical Biology

0 references

volume

8

0 references

issue

5

0 references

page(s)

428-430

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exact match

0 references

cites work

Charting biologically relevant chemical space: a structural classification of natural products (SCONP)

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Synthesis of natural-product-like molecules with over eighty distinct scaffolds

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Controlling the formation of 1 out of 64 stereoisomers using organocatalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Enantioselective polyene cyclization via organo-SOMO catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Enantioselective copper-catalyzed 1,3-dipolar cycloadditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

4,7-diphenylisobenzofuran: a useful intermediate for the construction of phenyl-substituted acenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Strained to the limit: when a cyclobutyl moiety becomes a thermodynamic sink in a protolytic ring-opening of photogenerated oxetanes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Control of four stereocentres in a triple cascade organocatalytic reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22426113

12 December 2020

inferred from PubMed ID database lookup

Highly Enantioselective Copper(I)−Fesulphos-Catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22426113

12 December 2020

inferred from PubMed ID database lookup

Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22426113

12 December 2020

inferred from PubMed ID database lookup

CuI–Fesulphos complexes: efficient chiral catalysts for asymmetric 1,3-dipolar cycloaddition of azomethine ylides

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

7 January 2021

inferred from DOI database lookup

Sulfenylphosphinoferrocenes: Novel planar chiral ligands in enantioselective catalysis

1 reference

https://api.crossref.org/works/10.1038%2FNCHEMBIO.901

7 January 2021