| Year |
Citation |
Score |
| 2019 |
Zacuto MJ. Synthesis of Acrylamides via the Doebner-Knoevenagel Condensation. The Journal of Organic Chemistry. PMID 30997800 DOI: 10.1021/acs.joc.9b00450 |
0.482 |
|
| 2017 |
Nielsen MK, Shields BJ, Liu J, Williams MJ, Zacuto MJ, Doyle AG. Mild, Redox-Neutral Formylation of Aryl Chlorides via Photocatalytic Generation of Chlorine Radicals. Angewandte Chemie (International Ed. in English). PMID 28471521 DOI: 10.1002/anie.201702079 |
0.317 |
|
| 2016 |
Mullens P, Cleator E, McLaughlin M, Bishop B, Edwards J, Goodyear A, Andreani T, Jin Y, Kong J, Li H, Williams M, Zacuto M. Two Approaches to the Chemical Development and Large-Scale Preparation of a Pyrimidyl Tetrazole Intermediate Organic Process Research & Development. 20: 1075-1087. DOI: 10.1021/Acs.Oprd.6B00136 |
0.415 |
|
| 2015 |
Chung JYL, Scott JP, Anderson C, Bishop B, Bremeyer N, Cao Y, Chen Q, Dunn R, Kassim A, Lieberman D, Moment AJ, Sheen F, Zacuto M. Evolution of a Manufacturing Route to Omarigliptin, A Long-Acting DPP-4 Inhibitor for the Treatment of Type 2 Diabetes Organic Process Research and Development. 19: 1760-1768. DOI: 10.1021/Acs.Oprd.5B00267 |
0.577 |
|
| 2015 |
Zacuto MJ, Dunn RF, Figus M. ChemInform Abstract: One-Step Synthesis of 1-Chloro-3-arylacetone Derivatives from Arylacetic Acids. Cheminform. 46: no-no. DOI: 10.1002/chin.201512070 |
0.343 |
|
| 2014 |
Xu F, Zacuto MJ, Kohmura Y, Rosen J, Gibb A, Alam M, Scott J, Tschaen D. Asymmetric synthesis of highly functionalized tetrahydropyran DPP-4 inhibitor. Organic Letters. 16: 5422-5. PMID 25269068 DOI: 10.1021/Ol502661G |
0.57 |
|
| 2014 |
Zacuto MJ, Dunn RF, Figus M. One-step synthesis of 1-chloro-3-arylacetone derivatives from arylacetic acids. The Journal of Organic Chemistry. 79: 8917-25. PMID 25184954 DOI: 10.1021/jo5016486 |
0.32 |
|
| 2012 |
Kong J, Chen CY, Balsells-Padros J, Cao Y, Dunn RF, Dolman SJ, Janey J, Li H, Zacuto MJ. Synthesis of the HCV protease inhibitor Vaniprevir (MK-7009) using ring-closing metathesis strategy. The Journal of Organic Chemistry. 77: 3820-8. PMID 22458448 DOI: 10.1021/Jo3001595 |
0.367 |
|
| 2010 |
Xu F, Zacuto M, Yoshikawa N, Desmond R, Hoerrner S, Itoh T, Journet M, Humphrey GR, Cowden C, Strotman N, Devine P. Asymmetric synthesis of telcagepant, a CGRP receptor antagonist for the treatment of migraine. The Journal of Organic Chemistry. 75: 7829-41. PMID 20954694 DOI: 10.1021/Jo101704B |
0.397 |
|
| 2010 |
Xu F, Corley E, Zacuto M, Conlon DA, Pipik B, Humphrey G, Murry J, Tschaen D. Asymmetric synthesis of a potent, aminopiperidine-fused imidazopyridine dipeptidyl peptidase IV inhibitor. The Journal of Organic Chemistry. 75: 1343-53. PMID 20128619 DOI: 10.1021/Jo902573Q |
0.575 |
|
| 2010 |
Zacuto MJ, Tomita D, Pirzada Z, Xu F. Chemoselectivity of the Ru-catalyzed cycloisomerization reaction for the synthesis of dihydropyrans; application to the synthesis of L-forosamine. Organic Letters. 12: 684-7. PMID 20088537 DOI: 10.1021/ol9026667 |
0.508 |
|
| 2009 |
Leighton J, Spletstoser J, Zacuto M. Methodology for the Synthesis of Polyketide Fragments Synfacts. 2009: 0301-0301. DOI: 10.1055/S-0028-1087752 |
0.636 |
|
| 2009 |
Hirner JJ, Zacuto MJ. 7-Chloroquinoline: a versatile intermediate for the synthesis of 7-substituted quinolines Tetrahedron Letters. 50: 4989-4993. DOI: 10.1016/j.tetlet.2009.06.077 |
0.474 |
|
| 2008 |
Spletstoser JT, Zacuto MJ, Leighton JL. Tandem silylformylation - Crotylsilylation/tamao oxidation of internal alkynes: A remarkable example of generating complexity from simplicity Organic Letters. 10: 5593-5596. PMID 19007175 DOI: 10.1021/Ol802489W |
0.663 |
|
| 2007 |
Zacuto MJ, Xu F. One-step RhCl3-catalyzed deprotection of acyclic N-allyl amides. The Journal of Organic Chemistry. 72: 6298-300. PMID 17625881 DOI: 10.1002/chin.200751055 |
0.305 |
|
| 2005 |
Zacuto MJ, Leighton JL. Divergent synthesis of complex polyketide-like macrolides from a simple polyol fragment Organic Letters. 7: 5525-5527. PMID 16288547 DOI: 10.1021/Ol052373G |
0.589 |
|
| 2003 |
Zacuto MJ, O'Malley SJ, Leighton JL. Tandem silylformylation-allyl(crotyl)silylation: A new approach to polyketide synthesis Tetrahedron. 59: 8889-8900. DOI: 10.1016/J.Tet.2003.04.004 |
0.632 |
|
| 2002 |
Zacuto MJ, O'Malley SJ, Leighton JL. Tandem intramolecular silylformylation-crotylsilylation: Highly efficient synthesis of polyketide fragments Journal of the American Chemical Society. 124: 7890-7891. PMID 12095319 DOI: 10.1021/Ja026511Y |
0.629 |
|
| 2000 |
Zacuto MJ, Leighton JL. Tandem intramolecular silylformylation-allylsilylation [15] Journal of the American Chemical Society. 122: 8587-8588. DOI: 10.1021/Ja002425R |
0.646 |
|
| 2000 |
Zacuto MJ, Leighton JL. ChemInform Abstract: Tandem Intramolecular Silylformylation-Allylsilylation. Cheminform. 31: no-no. DOI: 10.1002/chin.200049085 |
0.611 |
|
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