| Wittig Reactions in Water Media Employing Stabilized Ylides with Aldehydes. Synthesis of α,β-Unsaturated Esters from Mixing Aldehydes, α-Bromoesters, and Ph3P in … A El-Batta, C Jiang, W Zhao, R Anness, AL Cooksy, M Bergdahl The Journal of organic chemistry 72 (14), 5244-5259, 2007 | 223 | 2007 |
| Structure of a hepatitis C virus RNA domain in complex with a translation inhibitor reveals a binding mode reminiscent of riboswitches SM Dibrov, K Ding, ND Brunn, MA Parker, BM Bergdahl, DL Wyles, ... Proceedings of the National Academy of Sciences 109 (14), 5223-5228, 2012 | 115 | 2012 |
| Water is an efficient medium for Wittig reactions employing stabilized ylides and aldehydes J Dambacher, W Zhao, A El-Batta, R Anness, C Jiang, M Bergdahl Tetrahedron letters 46 (26), 4473-4477, 2005 | 113 | 2005 |
| Chloro-and iodotrimethylsilane-activated additions of organocopper compounds to enones and enoates M Bergdahl, EL Lindstedt, M Nilsson, T Olsson Tetrahedron 44 (7), 2055-2062, 1988 | 87 | 1988 |
| Iodotrimethylsilane-promoted additions of monoorganocopper compounds to. alpha.,. beta.-unsaturated ketones, esters, and lactones M Bergdahl, M Eriksson, M Nilsson, T Olsson The Journal of Organic Chemistry 58 (25), 7238-7244, 1993 | 75 | 1993 |
| Organocopper-iodosilane combinations in conjugate additions M Bergdahl, EL Lindstedt, M Nilsson, T Olsson Tetrahedron 45 (2), 535-543, 1989 | 57 | 1989 |
| Highly diastereoselective conjugate additions of monoorganocopper reagents to chiral imides J Dambacher, R Anness, P Pollock, M Bergdahl Tetrahedron 60 (9), 2097-2110, 2004 | 52 | 2004 |
| Highly diastereoselective additions of organocopper reagents to 2-exo-bornyl crotonates M Bergdahl, M Nilsson, T Olsson, K Stern Tetrahedron 47 (46), 9691-9702, 1991 | 38 | 1991 |
| Synthesis of the oxazole-and diene-containing C9–C23 fragment of the type a streptogramin antibiotics M Bergdahl, R Hett, TL Friebe, AR Gangloff, J Iqbal, Y Wu, P Helquist Tetrahedron letters 34 (46), 7371-7374, 1993 | 37 | 1993 |
| Conjugate Additions of a Simple Monosilylcopper Reagent with Use of the CuI⊙ DMS Complex: Stereoselectivities and a Dramatic Impact by DMS J Dambacher, M Bergdahl The Journal of Organic Chemistry 70 (2), 580-589, 2005 | 36 | 2005 |
| Asymmetric conjugate additions of TMSI promoted monoorganocuprate reagents, Li [RCuI], to various N-enoyl oxazolidinones P Pollock, J Dambacher, R Anness, M Bergdahl Tetrahedron letters 43 (20), 3693-3697, 2002 | 34 | 2002 |
| Diastereoselectivity in iodotrimethylsilane-promoted conjugate additions of organocopper reagents to chiral α, β-unsaturated imides and amides M Bergdahl, T Iliefski, M Nilsson, T Olsson Tetrahedron letters 36 (18), 3227-3230, 1995 | 33 | 1995 |
| NMR studies of TMS-halide activated organocopper compounds M Bergdahl, EL Lindstedt, T Olsson Journal of organometallic chemistry 365 (3), C11-C14, 1989 | 32 | 1989 |
| Direct copper (I) iodide dimethyl sulfide catalyzed conjugate addition of alkenyl groups from vinylzirconocene reagents A El-Batta, TR Hage, S Plotkin, M Bergdahl Organic Letters 6 (1), 107-110, 2004 | 31 | 2004 |
| Stereoselective conjugate addition of TMSI-activated butylcopper to 1-(R)-endo-(1-naphthyl) bornyl crotonate M Bergdahl, M Nilsson, T Olsson Journal of organometallic chemistry 391 (2), C19-C22, 1990 | 30 | 1990 |
| Stereocontrolled synthesis of the spirocyclic alkaloid (±)-nitramine D Tanner, HH Ming, M Bergdahl Tetrahedron letters 29 (49), 6493-6495, 1988 | 30 | 1988 |
| The Remarkable Ability of Lithium Ion To Reverse the Stereoselectivity in the Conjugate Addition of Li[BuCuI] to a Chiral N-Crotonyl-2-oxazolidinone J Dambacher, M Bergdahl Organic Letters 5 (19), 3539-3541, 2003 | 25 | 2003 |
| Synthesis of macrocyclic lactam/lactone derivatives having antimicrobial activity P Helquist, M Bergdahl, R Hett, AR Gangloff, M Demillequand, M Cottard, ... Pure and applied chemistry 66 (10-11), 2063-2066, 1994 | 20 | 1994 |
| Employing the simple monosilylcopper reagent, Li [PhMe 2 SiCuI], in 1, 4-addition reactions J Dambacher, M Bergdahl Chemical communications, 144-145, 2003 | 16 | 2003 |
| Further insight into the asymmetric vinylogous Mukaiyama aldol reaction (VMAR); application to the synthesis of the C27–C45 segment of lagunamide A BA Banasik, L Wang, A Kanner, BM Bergdahl Tetrahedron 72 (19), 2481-2490, 2016 | 15 | 2016 |
