Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yatao Lang"'
Publikováno v:
Green Synthesis and Catalysis, Vol 3, Iss 4, Pp 373-376 (2022)
Acyl fluorides are powerful synthons for acylation with wide application in the synthesis of valued compounds, especially peptides. Herein, a practical and catalyst-free method for the synthesis of acyl fluorides from aldehydes via C(sp2)–H fluorin
Externí odkaz:
https://doaj.org/article/761a29e042f548c2950e7ec8a84a437c
Publikováno v:
Fundamental Research, Vol 1, Iss 6, Pp 742-746 (2021)
Transition-metal catalyzed cross-couplings of aryl halides (ArI, ArBr and ArCl) with a broad range of nucleophiles have been developed as powerful methods for carbon–carbon and carbon–heteroatom bonds formation. However, due to the high bond diss
Externí odkaz:
https://doaj.org/article/b235cc3263e64af9889e2cb7dfa10a08
Publikováno v:
Chemical Science; 8/28/2024, Vol. 15 Issue 32, p12900-12905, 6p
Publikováno v:
CCS Chemistry. 4:3254-3263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2339e662c8019eb2dce10413c9bf6094
https://doi.org/10.31635/ccschem.022.202101685
https://doi.org/10.31635/ccschem.022.202101685
Publikováno v:
Fundamental Research. 1:742-746
Transition-metal catalyzed cross-couplings of aryl halides (ArI, ArBr and ArCl) with a broad range of nucleophiles have been developed as powerful methods for carbon–carbon and carbon–heteroatom bonds formation. However, due to the high bond diss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99adf360bb2a4b626913130c81748798
https://doi.org/10.1016/j.fmre.2021.06.018
https://doi.org/10.1016/j.fmre.2021.06.018
Publikováno v:
Organic Chemistry Frontiers. 8:3594-3613
Currently, photoreactions have become powerful synthetic tools with a broad scope of application. However, many photoreactions require the addition of transition-metal catalysts (Ni, Cu and so on) and photosensitizers (Ir and Ru complexes, and organi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c63a6d27eec511f0bdf82052ac87553
https://doi.org/10.1039/d1qo00359c
https://doi.org/10.1039/d1qo00359c
Publikováno v:
Green Chemistry. 22:6323-6327
Herein, novel photoinduced catalyst-free deborylation–deuteration of arylboronic acids with D2O is reported. The protocol was compatible with a variety of functionalities, including halogen, alkoxy, cyano, sulfonyl, trimethylsilyl, trifluoromethoxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e35209c279f56dae181c8c5dfe7dce8
https://doi.org/10.1039/d0gc01649g
https://doi.org/10.1039/d0gc01649g
Publikováno v:
Chemical science. 13(3)
A visible-light-induced, transition-metal and external photosensitizer free decarbonylative addition of benzaldehydes to ketones/aldehydes via anion intermediates at room temperature is developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2cc82beb9c4cdd23a88a524a97e013
https://pubmed.ncbi.nlm.nih.gov/35173934
https://pubmed.ncbi.nlm.nih.gov/35173934