Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Andrew J. Musacchio"'
Autor:
David C. Miller, Trevor C. Sherwood, Andrew J. Musacchio, Jacob M. Ganley, Robert R. Knowles, William R. Ewing
Publikováno v:
J Am Chem Soc
We report here a photocatalytic method for the intermolecular anti-Markovnikov hydroamination of unactivated olefins with primary alkyl amines to selectively furnish secondary amine products. These reactions proceed through aminium radical cation (AR
Publikováno v:
J Am Chem Soc
With hundreds of unique members isolated to date, guaianolide lactones represent a particularly prolific class of terpene natural products. Given their extensive documented therapeutic properties and fascinating chemical structures, these metabolites
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a800c7e63ed412700d4b166ab94e378
https://europepmc.org/articles/PMC6818654/
https://europepmc.org/articles/PMC6818654/
Publikováno v:
Journal of the American Chemical Society. 136:12217-12220
While olefin amination with aminium radical cations is a classical method for C-N bond formation, catalytic variants that utilize simple 2° amine precursors remain largely undeveloped. Herein we report a new visible-light photoredox protocol for the
Autor:
Trevor C. Sherwood, Saeed G. Naguib, Robert R. Knowles, Andrew J. Musacchio, Brendan C. Lainhart, Xin Zhang
Publikováno v:
Science (New York, N.Y.). 355(6326)
Hydroamination gets a light push uphill Hydroamination of olefins is a broadly useful method for making carbon-nitrogen bonds. However, when both the amine and the olefin have multiple alkyl substituents, the reaction can become energetically unfavor
Autor:
Timothy Noël, Andrew J. Musacchio
Publikováno v:
Organic Letters. 13:5180-5183
General continuous-flow conditions for the Suzuki-Miyaura cross-coupling of heteroaryl halides and (hetero)arylboronic acids have been developed. A wide range of heterobiaryl products is obtained in excellent yields (20 examples) employing low cataly
Publikováno v:
ChemInform. 46
While olefin amination with aminium radical cations is a classical method for C–N bond formation, catalytic variants that utilize simple 2° amine precursors remain largely undeveloped. Herein we report a new visible-light photoredox protocol for t
Autor:
Timothy Noël, Andrew J. Musacchio
Publikováno v:
ChemInform. 43
The reaction is applied to a wide range of heteroaromatic chlorides, bromides and triflates and aromatic and heteroaromatic boronic acids.
Publikováno v:
ChemInform. 42
A continuous-flow microfluidic system is developed for the transformation of phenols into their corresponding aryl triflates followed by Suzuki—Miyaura cross-coupling reaction to afford biaryls directly.
Autor:
Timothy NoeÌl, Andrew J. Musacchio
Publikováno v:
Organic Letters; Oct2011, Vol. 13 Issue 19, p5180-5183, 4p