Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Massimo Brochetta"'
Autor:
Arun Maji, Amit Dahiya, Gang Lu, Trisha Bhattacharya, Massimo Brochetta, Giuseppe Zanoni, Peng Liu, Debabrata Maiti
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Electrophilic acylation of arenes is largely limited to electron rich systems, non-polar medium and often displays moderate selectivity. Here, the authors show a directed para-selective ketonisation of arenes, overriding electronic bias and structura
Externí odkaz:
https://doaj.org/article/f8e52a1b27b94288a6c5af4e4c47e1b5
Autor:
Massimo Brochetta, Giuseppe Zanoni, Debabrata Maiti, Tuhin Patra, Tania Borsari, Prakriti Kalra, Emanuele Casali, Andrea Gandini
Publikováno v:
Chemical communications (Cambridge, England). 56(53)
An orthogonal selectivity for distal meta-C–H activation of benzophenone is acheived by overriding the inherent proximal ortho-selectivity through a template assisted metalation approach. This strategy has been successfully utilized in Pd-catalyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17cb2b8baec7a742954b24aa1e42541c
https://pubmed.ncbi.nlm.nih.gov/32478359
https://pubmed.ncbi.nlm.nih.gov/32478359
Autor:
Giuseppe Zanoni, Massimo Brochetta, Peng Liu, Arun Maji, Debabrata Maiti, Gang Lu, Amit Dahiya, Trisha Bhattacharya
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Nature Communications
Nature Communications
In nature, enzymatic pathways generate Caryl−C(O) bonds in a site-selective fashion. Synthetically, Caryl−C(O) bonds are synthesised in organometallic reactions using prefunctionalized substrate materials. Electrophilic routes are largely limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a349e488fdcc8d77187d7ba13a81cd92
https://doaj.org/article/f8e52a1b27b94288a6c5af4e4c47e1b5
https://doaj.org/article/f8e52a1b27b94288a6c5af4e4c47e1b5
Autor:
Daniel B. Werz, Debabrata Maiti, Sukdev Bag, Giuseppe Zanoni, Siddhartha Maiti, Alessio Porta, Tania Borsari, Massimo Brochetta, Sadhan Jana
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(44)
The development of efficient and mild methods for the synthesis of organofluorine compounds is of foremost interest in various fields of chemistry. A direct pyrimidine-based selective meta-C-H perfluoroalkenylation of arenes involving several commerc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afb2e9a7cc4b11ca3b36aae7541eaaf
https://pubmed.ncbi.nlm.nih.gov/31215707
https://pubmed.ncbi.nlm.nih.gov/31215707