Selective aromatization of the A-ring of steroids through carbon-carbon, carbon-hydrogen, and carbon-oxygen bond activation by an electrophilic ruthenium complex

1993 ◽  
Vol 115 (9) ◽  
pp. 3484-3493 ◽  
Author(s):  
Francisco Urbanos ◽  
Malcolm A. Halcrow ◽  
Juan Fernandez-Baeza ◽  
Francoise Dahan ◽  
Daniel Labroue ◽  
...  
2007 ◽  
Vol 26 (20) ◽  
pp. 4881-4889 ◽  
Author(s):  
Ian J. Blackmore ◽  
Christopher J. Semiao ◽  
Miriam S. A. Buschhaus ◽  
Brian O. Patrick ◽  
Peter Legzdins

2012 ◽  
Vol 31 (14) ◽  
pp. 5018-5024 ◽  
Author(s):  
Kimberly A. Manbeck ◽  
Sabuj Kundu ◽  
Aaron P. Walsh ◽  
William W. Brennessel ◽  
William D. Jones
Keyword(s):  

RSC Advances ◽  
2016 ◽  
Vol 6 (103) ◽  
pp. 101259-101266 ◽  
Author(s):  
Ilnett García-Ventura ◽  
Marcos Flores-Alamo ◽  
Juventino J. García

The reaction between [(dippe)NiH]2 (1) (dippe = 1,2-bis(diisopropylphosphino)-ethane) and 2- and 3-furonitrile (2-FN and 3-FN) was carried out at room temperature.


2008 ◽  
Vol 27 (15) ◽  
pp. 3681-3692 ◽  
Author(s):  
Samat Tussupbayev ◽  
Sergei F. Vyboishchikov

Synlett ◽  
2018 ◽  
Vol 29 (13) ◽  
pp. 1729-1734 ◽  
Author(s):  
Zhi-Qiang Wang ◽  
Xin-Qi Hao ◽  
Chen Xu ◽  
Hong-Mei Li ◽  
Tian-Yong Tu ◽  
...  

Selective monoarylation of naphthylpyrimidines with a variety of aryl chlorides through C–H bond activation in water was achieved by using a water-soluble [RuCl2-(η6-PhOCH2CH2OH)]2/phosphine catalytic system. The monoarylation occurred at the C-2 carbon of the naphthalene moiety, and selectively polysubstituted naphthylpyrimidines were obtained by a one-pot reaction involving a subsequent hetarylation with 2-pyridyl chlorides.


2017 ◽  
Vol 36 (18) ◽  
pp. 3654-3663 ◽  
Author(s):  
Samantha Lau ◽  
Bryan Ward ◽  
Xueer Zhou ◽  
Andrew J. P. White ◽  
Ian J. Casely ◽  
...  

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