Year |
Citation |
Score |
2008 |
Sun C, Wang Q, Brubaker JD, Wright PM, Lerner CD, Noson K, Charest M, Siegel DR, Wang YM, Myers AG. A robust platform for the synthesis of new tetracycline antibiotics. Journal of the American Chemical Society. 130: 17913-27. PMID 19053822 DOI: 10.1021/Ja806629E |
0.617 |
|
2006 |
Lipshutz BH, Lower A, Kucejko RJ, Noson K. Applications of asymmetric hydrosilylations mediated by catalytic (DTBM-SEGPHOS)CuH. Organic Letters. 8: 2969-72. PMID 16805529 DOI: 10.1021/Ol060854+ |
0.735 |
|
2006 |
Lipshutz B, Lower A, Kucejko R, Noson K. Cu-Catalyzed Asymmetric Hydrosilylations of Ketones Synfacts. 2006: 0935-0935. DOI: 10.1055/S-2006-949212 |
0.687 |
|
2004 |
Lipshutz BH, Buzard DJ, Olsson C, Noson K. A modular route to nonracemic cyclo-NOBINs. Preparation of the parent ligand for homo- and heterogeneous catalysis Tetrahedron. 60: 4443-4449. DOI: 10.1016/J.Tet.2004.02.065 |
0.559 |
|
2003 |
Lipshutz BH, Noson K, Chrisman W, Lower A. Asymmetric hydrosilylation of aryl ketones catalyzed by copper hydride complexed by nonracemic biphenyl bis-phosphine ligands. Journal of the American Chemical Society. 125: 8779-89. PMID 12862472 DOI: 10.1021/Ja021391F |
0.742 |
|
2002 |
Lipshutz BH, Lower A, Noson K. Copper(I) hydride-catalyzed asymmetric hydrosilylation of heteroaromatic ketones. Organic Letters. 4: 4045-8. PMID 12423082 DOI: 10.1021/Ol026755N |
0.761 |
|
2001 |
Lipshutz BH, Noson K, Chrisman W. Ligand-accelerated, copper-catalyzed asymmetric hydrosilylations of aryl ketones. Journal of the American Chemical Society. 123: 12917-8. PMID 11749557 DOI: 10.1021/Ja011529E |
0.774 |
|
2001 |
Lipshutz BH, Chrisman W, Noson K. Hydrosilylation of aldehydes and ketones catalyzed by [Ph3P(CuH)]6 Journal of Organometallic Chemistry. 624: 367-371. DOI: 10.1016/S0022-328X(00)00903-7 |
0.761 |
|
2000 |
Lipshutz BH, Chrisman W, Noson K, Papa P, Sclafani JA, Vivian RW, Keith JM. Copper hydride-catalyzed tandem 1,4-reduction/alkylation reactions Tetrahedron. 56: 2779-2788. DOI: 10.1016/S0040-4020(00)00132-0 |
0.612 |
|
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