Effective asymmetric hydroboration catalysed by a rhodium complex of 1-(2-diphenylphosphino-1-naphthyl)isoquinoline

Author(s):  
John M. Brown ◽  
David I. Hulmes ◽  
Timothy P. Layzell
Synlett ◽  
2020 ◽  
Author(s):  
Shi-Liang Shi ◽  
Yuan Cai

AbstractAsymmetric hydroboration of simple and unactivated terminal alkenes (α-olefins), feedstock chemicals derived from the petrochemical industry, has not been efficiently realized for past decades. Using a bulky ANIPE ligand, we achieved a rare example of highly enantioselective copper-catalyzed Markovnikov hydroboration of α-olefins. The chiral secondary alkylboronic ester products were obtained in moderate to good yields and regioselectivities with excellent enantioselectivities.1 Introduction2 Conditions Optimization3 Substrate Scope4 Application5 Mechanistic Discussion6 Conclusions and Future Directions


2013 ◽  
Vol 17 (14) ◽  
pp. 1499-1506 ◽  
Author(s):  
Alex Hamilton ◽  
Michael Gicquel ◽  
Pablo Ballester ◽  
Carles Bo

2005 ◽  
Vol 34 (11) ◽  
pp. 1480-1481 ◽  
Author(s):  
Tamio Hayashi ◽  
Norihito Tokunaga ◽  
Kazuhiro Okamoto ◽  
Ryo Shintani

1991 ◽  
Vol 46 (6) ◽  
pp. 783-788 ◽  
Author(s):  
Christian Egger ◽  
Ulrich Schubert

A heterogenized rhodium complex, prepared by sol-gel processing of Rh(CO)Cl[PPh2CH2CH2Si(OEt)3]2 and Si(OEt)4, is shown to catalyze the conversion of the silanes H4-nSiPh„ (n = 1 - 3) or (HMe2Si)2O to (poly)siloxanes by air or water. Using THF as a solvent, the silanoles Ph3SiOH or Ph2Si(OH)2 are obtained instead. The reaction of phenylacetic acid or acetic acid with HSiPh3 to give silyl esters is catalyzed by the same compound.


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