Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Meike Niggemann"'
Publikováno v:
Chemistry – A European Journal. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef741f6f14082e1cada83d0bbb85bfd8
https://doi.org/10.1002/chem.202202477
https://doi.org/10.1002/chem.202202477
Publikováno v:
Chemistry-a European journal 28(53), e202201830 (2022). doi:10.1002/chem.202201830
Chemistry - a European journal (2022). doi:10.1002/chem.202201830
Published by Wiley-VCH, Weinheim
Published by Wiley-VCH, Weinheim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::409ed19323110786cf15423ac3f9cff1
https://pubmed.ncbi.nlm.nih.gov/35793203
https://pubmed.ncbi.nlm.nih.gov/35793203
Publikováno v:
Early Main Group Metal Catalysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df6d73faa9e350349fb5109a22bc369b
https://doi.org/10.1002/9783527818020.ch11
https://doi.org/10.1002/9783527818020.ch11
Publikováno v:
Angewandte Chemie International Edition. 58:6713-6717
A rare reductive coupling of nitro compounds with organohalides has been realized. The reaction is initiated by a partial reduction of the nitro group to a nitrenoid intermediate. Therefore, not only aromatic but also aliphatic nitro compounds are ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd64939aa6698ef1470a40df4f7d31c5
https://doi.org/10.1002/anie.201814197
https://doi.org/10.1002/anie.201814197
Publikováno v:
Angewandte Chemie International Edition. 58:5119-5123
A new concept for selectivity control in carbocation-driven reactions has been identified which allows for the chemo-, regio-, and stereoselective addition of nucleophiles to alkynes-assisted vinyl cation formation-enabled by a Li+ -based supramolecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24d3f4b2c9c18e11061583e998bb855b
https://doi.org/10.1002/anie.201810916
https://doi.org/10.1002/anie.201810916
Publikováno v:
Angewandte Chemie. 131:5173-5177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11317cc99e7c2d5a57bdd2dc430c5370
https://doi.org/10.1002/ange.201810916
https://doi.org/10.1002/ange.201810916
Autor:
Shuang Gao, Meike Niggemann
Publikováno v:
Advanced Synthesis & Catalysis. 361:1549-1553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc63c18cfd4d79a210788bd5614a3630
https://doi.org/10.1002/adsc.201801407
https://doi.org/10.1002/adsc.201801407
Publikováno v:
Angewandte Chemie. 130:6005-6009
In analogy to the classical reaction of C-B bonds with peroxides, the first oxidative functionalization of aminoboranes through a 1,2-N migration was realized. Readily available aliphatic nitro compounds are thereby transformed into N- and O-function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::002de40b56ad91c522a164f27cc2b13b
https://doi.org/10.1002/ange.201803168
https://doi.org/10.1002/ange.201803168
Publikováno v:
Chemistry - A European Journal. 24:3970-3974
The first general protocol for the direct reductive N-functionalization of aliphatic nitro compounds is presented. The nitro group is partially reduced to a nitrenoid, with a mild and readily available combination of B2 pin2 and zinc organyls. Thereb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0e07cec46123774227977dc503e09c
https://doi.org/10.1002/chem.201705986
https://doi.org/10.1002/chem.201705986
Publikováno v:
Angewandte Chemie. 129:13454-13458
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45b79f1abc41338cbc0e17cf5b07fc00
https://doi.org/10.1002/ange.201705964
https://doi.org/10.1002/ange.201705964