Iridium‐Catalyzed Regio‐ and Enantioselective Borylation of Unbiased Methylene C(sp3)‐H Bonds at the Position Beta to a Nitrogen Center

Author(s):  
Rongrong Du ◽  
Luhua Liu ◽  
Senmiao Xu
Keyword(s):  
2016 ◽  
Vol 45 (18) ◽  
pp. 7829-7835 ◽  
Author(s):  
Carmina Alfonso ◽  
Marta Feliz ◽  
Vicent S. Safont ◽  
Rosa Llusar

The reaction between Mo3S4Cl4(PPh)3(H2O)2 and (R)-PPro or (S)-PPro is diastereoselective towards the (P)-Mo3S4 configuration with the preservation of the aminophosphine chirality and the formation of a stereogenic nitrogen center.


2017 ◽  
Vol 19 (9) ◽  
pp. 2406-2409 ◽  
Author(s):  
Haizhen Jiang ◽  
Yunrong Chen ◽  
Bo Chen ◽  
Hui Xu ◽  
Wen Wan ◽  
...  

2002 ◽  
Vol 643-644 ◽  
pp. 98-104 ◽  
Author(s):  
Christine Saluzzo ◽  
Jérémy Breuzard ◽  
Stéphane Pellet-Rostaing ◽  
Martial Vallet ◽  
Frédéric Le Guyader ◽  
...  

Tetrahedron ◽  
2017 ◽  
Vol 73 (27-28) ◽  
pp. 3823-3830 ◽  
Author(s):  
Piotr Kaszyński ◽  
Arkadiusz Kłys ◽  
Sławomir Domagała ◽  
Krzysztof Woźniak

1976 ◽  
Vol 7 (27) ◽  
pp. no-no
Author(s):  
J. BJOERGO ◽  
D. R. BOYD ◽  
R. M. CAMPBELL ◽  
D. C. NEILL
Keyword(s):  

2013 ◽  
Vol 9 ◽  
pp. 1419-1425 ◽  
Author(s):  
Steven S Y Wong ◽  
Michael G Brant ◽  
Christopher Barr ◽  
Allen G Oliver ◽  
Jeremy E Wulff

Dipolar addition of cyclic azomethine imines with cyclic vinyl sulfones gave rise to functionalized tricycles that exhibited fluxional behavior in solution at room temperature. The scope of the synthetic methodology was explored, and the origin of the fluxional behavior was probed by NMR methods together with DFT calculations. This behavior was ultimately attributed to stereochemical inversion at one of two nitrogen centers embedded in the tricyclic framework. Two tetracycles were also synthesized, and the degree of signal-broadening in the NMR spectra was found to depend on the presence of substitution next to the inverting nitrogen center.


2010 ◽  
Vol 39 (3) ◽  
pp. 303-308 ◽  
Author(s):  
V. A. Nadolinny ◽  
V. V. Golushko ◽  
O. P. Yuryeva ◽  
M. I. Rakhmanova ◽  
V. S. Shatsky
Keyword(s):  

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