Zobrazeno 1 - 10
of 286
pro vyhledávání: '"Eduard Hartmann"'
Publikováno v:
Nature Chemistry. 6:1056-1064
The stereocontrolled introduction of vicinal heteroatomic substituents into organic molecules is one of the most powerful ways of adding value and function. Although many methods exist for the introduction of oxygen- and nitrogen-containing substitue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6de142d358d4b09731e7991ee8ce09c0
https://doi.org/10.1038/nchem.2109
https://doi.org/10.1038/nchem.2109
Publikováno v:
Chemical Reviews. 113:402-441
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3db9746e8437a65642faca3070ad0d7b
https://doi.org/10.1021/cr3003517
https://doi.org/10.1021/cr3003517
Autor:
Eduard Hartmann, Martin Oestreich
Publikováno v:
Organic Letters. 14:2406-2409
The two-directional desymmetrization of prochiral precursors with α,β-unsaturated branches by catalyst-controlled 1,4-addition of silicon and likewise boron nucleophiles allows for a general enantioselective access to syn,anti-triols with 1,n + 1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aab859940740cf0689c8db34153080c9
https://doi.org/10.1021/ol300832f
https://doi.org/10.1021/ol300832f
Autor:
Martin Oestreich, Eduard Hartmann
Publikováno v:
Angewandte Chemie International Edition. 49:6195-6198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ccb384d5ec44c95a374aefcfe350f6
https://doi.org/10.1002/anie.201002916
https://doi.org/10.1002/anie.201002916
Autor:
Eduard Hartmann, Martin Oestreich
Publikováno v:
Angewandte Chemie. 122:6331-6334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0781fa45c6e2b23e52ec854f992702fd
https://doi.org/10.1002/ange.201002916
https://doi.org/10.1002/ange.201002916
Publikováno v:
ChemInform. 46
The stereocontrolled introduction of vicinal heteroatomic substituents into organic molecules is one of the most powerful ways of adding value and function. Although many methods exist for the introduction of oxygen- and nitrogen-containing substitue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61c6433c4e35e1cdb00d64146acad90c
https://doi.org/10.1002/chin.201520088
https://doi.org/10.1002/chin.201520088
Autor:
Scott E. Denmark, Eduard Hartmann
Publikováno v:
Helvetica Chimica Acta. 100:e1700158
The full details of mechanistic investigation on enantioselective sulfenofunctionalization of alkenes under Lewis base catalysis are described. Solution spectroscopic identification of the catalytically active sulfenylating agent has been accomplishe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c21e23ca78df20c35bcf7e22181f1e14
https://doi.org/10.1002/hlca.201700158
https://doi.org/10.1002/hlca.201700158
Publikováno v:
ChemInform. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2eda5d0a18bb867147b5be3daf8fd2e
https://doi.org/10.1002/chin.201312252
https://doi.org/10.1002/chin.201312252
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(48)
Activation of the Si-B inter-element bond with copper(I) alkoxides produces copper-based silicon nucleophiles that react readily with aldehydes to yield α-silyl alcohols (that is, α-hydroxysilanes) after hydrolysis. Two independent protocols were d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc4fc74ac471adf054a623d636f8e236
https://pubmed.ncbi.nlm.nih.gov/22025369
https://pubmed.ncbi.nlm.nih.gov/22025369