| Year |
Citation |
Score |
| 2017 |
Bronner S, Lee D, Bacauanu V, Cyr P. A Novel Cascade Benzyne Nucleophilic Addition/Fries Rearrangement for Entry into 2,3-Disubstituted Phenols Synlett. 28: e2-e2. DOI: 10.1055/s-0036-1589495 |
0.332 |
|
| 2014 |
Bronner SM, Herbert MB, Patel PR, Marx VM, Grubbs RH. Ru-Based Z-Selective Metathesis Catalysts with Modified Cyclometalated Carbene Ligands. Chemical Science (Royal Society of Chemistry : 2010). 5: 4091-4098. PMID 25346842 DOI: 10.1039/C4Sc01541J |
0.328 |
|
| 2014 |
Nathel NF, Shah TK, Bronner SM, Garg NK. Total syntheses of indolactam alkaloids (-)-indolactam V, (-)-pendolmycin, (-)-lyngbyatoxin A, and (-)-teleocidin A-2. Chemical Science (Royal Society of Chemistry : 2010). 5: 2184-2190. PMID 24839542 DOI: 10.1039/C4Sc00256C |
0.632 |
|
| 2014 |
Bronner SM, Grubbs RH. Formal Anti-Markovnikov Hydroamination of Terminal Olefins. Chemical Science (Royal Society of Chemistry : 2010). 5. PMID 24327829 DOI: 10.1039/C3Sc51897C |
0.496 |
|
| 2014 |
Fine Nathel NF, Shah TK, Bronner SM, Garg NK. ChemInform Abstract: Total Syntheses of Indolactam Alkaloids (-)-Indolactam V (Ia), (-)-Pendolmycin (Ib), (-)-Lyngbyatoxin A (Ic), and (-)-Teleocidin A-2 (Id). Cheminform. 45: no-no. DOI: 10.1002/chin.201443203 |
0.526 |
|
| 2014 |
Bronner SM, Grubbs RH. ChemInform Abstract: Formal anti-Markovnikov Hydroamination of Terminal Olefins. Cheminform. 45: no-no. DOI: 10.1002/chin.201427063 |
0.332 |
|
| 2012 |
Bronner SM, Mackey JL, Houk KN, Garg NK. Steric effects compete with aryne distortion to control regioselectivities of nucleophilic additions to 3-silylarynes. Journal of the American Chemical Society. 134: 13966-9. PMID 22876797 DOI: 10.1021/Ja306723R |
0.539 |
|
| 2012 |
Goetz AE, Bronner SM, Cisneros JD, Melamed JM, Paton RS, Houk KN, Garg NK. An efficient computational model to predict the synthetic utility of heterocyclic arynes. Angewandte Chemie (International Ed. in English). 51: 2758-62. PMID 22307724 DOI: 10.1002/Anie.201108863 |
0.626 |
|
| 2011 |
Bronner SM, Goetz AE, Garg NK. Overturning indolyne regioselectivities and synthesis of indolactam V. Journal of the American Chemical Society. 133: 3832-5. PMID 21351773 DOI: 10.1021/Ja200437G |
0.682 |
|
| 2011 |
Bronner SM, Goetz AE, Garg NK. Understanding and modulating indolyne regioselectivities Synlett. 2599-2604. DOI: 10.1055/S-0031-1289561 |
0.656 |
|
| 2011 |
Bronner SM, Im GJ, Garg NK. ChemInform Abstract: Indoles and Indolizidines in Natural Product Synthesis Cheminform. 43: no-no. DOI: 10.1002/chin.201201250 |
0.5 |
|
| 2011 |
Bronner SM, Im GYJ, Garg NK. Indoles and Indolizidines Heterocycles in Natural Product Synthesis. 221-265. DOI: 10.1002/9783527634880.ch7 |
0.502 |
|
| 2010 |
Im GY, Bronner SM, Goetz AE, Paton RS, Cheong PH, Houk KN, Garg NK. Indolyne experimental and computational studies: synthetic applications and origins of selectivities of nucleophilic additions. Journal of the American Chemical Society. 132: 17933-44. PMID 21114321 DOI: 10.1021/Ja1086485 |
0.681 |
|
| 2010 |
Cheong PH, Paton RS, Bronner SM, Im GY, Garg NK, Houk KN. Indolyne and aryne distortions and nucleophilic regioselectivites. Journal of the American Chemical Society. 132: 1267-9. PMID 20058924 DOI: 10.1021/Ja9098643 |
0.522 |
|
| 2010 |
Bronner S, Garg NK. Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoro-methanesulfonate: A versatile precursor to o-benzyne (The Journal of Organic Chemistry (2009) 74 (8842) DOI: 10.1021/jo9020166) Journal of Organic Chemistry. 75: 1330. DOI: 10.1021/jo9025513 |
0.475 |
|
| 2009 |
Bronner SM, Garg NK. Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate: a versatile precursor to o-benzyne. The Journal of Organic Chemistry. 74: 8842-3. PMID 19852458 DOI: 10.1021/Jo9020166 |
0.497 |
|
| 2009 |
Bronner SM, Bahnck KB, Garg NK. Indolynes as electrophilic indole surrogates: fundamental reactivity and synthetic applications. Organic Letters. 11: 1007-10. PMID 19178159 DOI: 10.1021/Ol802958A |
0.554 |
|
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