Year |
Citation |
Score |
2022 |
Al Subeh ZY, Li T, Ustoyev A, Obike JC, West PM, Khin M, Burdette JE, Pearce CJ, Oberlies NH, Croatt MP. Semisynthesis of Hypothemycin Analogues Targeting the C8-C9 Diol. Journal of Natural Products. PMID 35834411 DOI: 10.1021/acs.jnatprod.2c00434 |
0.5 |
|
2022 |
Alam K, Li T, Hyatt IFD, Croatt MP. AlCl-catalyzed regioselective intermolecular α or γ mono- or α,γ bis-hydroalkoxylation of allenamides with alcohols. Organic & Biomolecular Chemistry. PMID 35660842 DOI: 10.1039/d2ob00844k |
0.449 |
|
2019 |
Abu Deiab GI, Croatt MP. Synthetic approaches to isocarbacyclin and analogues as potential neuroprotective agents against ischemic stroke. Bioorganic & Medicinal Chemistry. 27: 338-342. PMID 30545734 DOI: 10.1016/J.Bmc.2018.12.010 |
0.43 |
|
2018 |
Al-Huniti MH, Perez MA, Garr MK, Croatt MP. Palladium-Catalyzed Chemoselective Protodecarboxylation of Polyenoic Acids. Organic Letters. PMID 30481039 DOI: 10.1021/Acs.Orglett.8B03016 |
0.465 |
|
2018 |
Al-Huniti MH, Rivera-Chávez J, Colón KL, Stanley JL, Burdette JE, Pearce CJ, Oberlies NH, Croatt MP. Development and Utilization of a Palladium-Catalyzed Dehydration of Primary Amides To Form Nitriles. Organic Letters. PMID 30221526 DOI: 10.1021/Acs.Orglett.8B02422 |
0.479 |
|
2018 |
McPherson KE, Croatt MP, Morehead AT, Sargent AL. DFT Mechanistic Investigation of an Enantioselective Tsuji–Trost Allylation Reaction Organometallics. 37: 3791-3802. DOI: 10.1021/Acs.Organomet.8B00507 |
0.604 |
|
2017 |
Al-Huniti MH, Sullivan ZB, Stanley JL, Carson JA, Hyatt IFD, Hairston AC, Croatt MP. Hypervalent Iodonium Alkynyl Triflate Generated Phenylcyanocarbene and Its Reactivity with Aromatic Systems. The Journal of Organic Chemistry. PMID 28841312 DOI: 10.1021/Acs.Joc.7B01608 |
0.555 |
|
2017 |
Fakhouri L, Cook CD, Al-Huniti MH, Console-Bram LM, Hurst DP, Spano MBS, Nasrallah DJ, Caron MG, Barak LS, Reggio PH, Abood ME, Croatt MP. Design, synthesis and biological evaluation of GPR55 agonists. Bioorganic & Medicinal Chemistry. PMID 28673732 DOI: 10.1016/J.Bmc.2017.06.016 |
0.32 |
|
2017 |
Deiab GI, Al-Huniti MH, Hyatt IF, Nagy EE, Gettys KE, Sayed SS, Joliat CM, Daniel PE, Vummalaneni RM, Morehead AT, Sargent AL, Croatt MP. Decarboxylative and dehydrative coupling of dienoic acids and pentadienyl alcohols to form 1,3,6,8-tetraenes. Beilstein Journal of Organic Chemistry. 13: 384-392. PMID 28382176 DOI: 10.3762/Bjoc.13.41 |
0.43 |
|
2016 |
Meza-Aviña ME, Lingerfelt MA, Console-Bram LM, Gamage TF, Sharir H, Gettys KE, Hurst DP, Kotsikorou E, Shore DM, Caron MG, Rao N, Barak LS, Abood ME, Reggio PH, Croatt MP. Design, synthesis, and analysis of antagonists of GPR55: Piperidine-substituted 1,3,4-oxadiazol-2-ones. Bioorganic & Medicinal Chemistry Letters. PMID 26916440 DOI: 10.1016/J.Bmcl.2016.02.030 |
0.333 |
|
2016 |
Deiab GIA, Croatt MP. Chapter 3 - Step-Economical Synthesis of Clinprost and Analogs Utilizing a Novel Decarboxylation Reaction Strategies and Tactics in Organic Synthesis. 12: 95-117. DOI: 10.1016/B978-0-08-100756-3.00003-0 |
0.628 |
|
2015 |
Dempsey Hyatt IF, Nasrallah DJ, Maxwell MA, Hairston AC, Abdalhameed MM, Croatt MP. Formation and in situ reactions of hypervalent iodonium alkynyl triflates to form cyanocarbenes. Chemical Communications (Cambridge, England). 51: 5287-9. PMID 25558484 DOI: 10.1039/C4Cc08676G |
0.595 |
|
2015 |
Nasrallah DJ, Croatt MP. ChemInform Abstract: Rhodium(I)-Catalyzed [2 + 2 + 2 + 2] Cycloaddition of Diynes to Form Cyclooctatetraenes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201505036 |
0.376 |
|
2014 |
Nasrallah DJ, Croatt MP. Rhodium(I)-catalyzed [2+2+2+2] cycloaddition of diynes to form cyclooctatetraenes European Journal of Organic Chemistry. 2014: 3767-3772. DOI: 10.1002/Ejoc.201402109 |
0.527 |
|
2013 |
Hyatt IF, Nasrallah DJ, Croatt MP. Synthesis of hypervalent iodonium alkynyl triflates for the application of generating cyanocarbenes. Journal of Visualized Experiments : Jove. PMID 24056681 DOI: 10.3791/50886 |
0.551 |
|
2013 |
Althagafy HS, Meza-Aviña ME, Oberlies NH, Croatt MP. Mechanistic study of the biomimetic synthesis of flavonolignan diastereoisomers in milk thistle. The Journal of Organic Chemistry. 78: 7594-600. PMID 23876147 DOI: 10.1021/Jo4011377 |
0.385 |
|
2013 |
Nagy EE, Hyatt IF, Gettys KE, Yeazell ST, Frempong SK, Croatt MP. Sequential Pd(0)-, Rh(I)-, and Ru(II)-catalyzed reactions in a nine-step synthesis of clinprost. Organic Letters. 15: 586-9. PMID 23327495 DOI: 10.1021/Ol303402E |
0.593 |
|
2013 |
Meza-Aviña ME, Patel MK, Croatt MP. Exploring the reactivity of 1,5-disubstituted sulfonyl-triazoles: Thermolysis and Rh(II)-catalyzed synthesis of α-sulfonyl nitriles This article is dedicated to Professor Paul Wender for both his creative contributions to synthetic organic chemistry and untiring mentorship Tetrahedron. 69: 7840-7846. DOI: 10.1016/J.Tet.2013.05.048 |
0.49 |
|
2012 |
Hyatt IF, Croatt MP. Reactions of hypervalent iodonium alkynyl triflates with azides: generation of cyanocarbenes. Angewandte Chemie (International Ed. in English). 51: 7511-4. PMID 22730261 DOI: 10.1002/Anie.201203062 |
0.569 |
|
2012 |
Hyatt IFD, Meza-Aviña ME, Croatt MP. Alkynes and azides: Not just for click reactions Synlett. 23: 2869-2874. DOI: 10.1055/S-0032-1317545 |
0.594 |
|
2012 |
Hyatt IFD, Croatt MP, Banert K, Arnold R, Hagedorn M, Thoss P, Auer AA. Cover Picture: Reactions of Hypervalent Iodonium Alkynyl Triflates with Azides: Generation of Cyanocarbenes / 1-Azido-1-Alkynes: Synthesis and Spectroscopic Characterization of Azidoacetylene (Angew. Chem. Int. Ed. 30/2012) Angewandte Chemie International Edition. 51: 7335-7335. DOI: 10.1002/Anie.201204825 |
0.591 |
|
2011 |
Meza-Aviña ME, Patel MK, Lee CB, Dietz TJ, Croatt MP. Selective formation of 1,5-substituted sulfonyl triazoles using acetylides and sulfonyl azides. Organic Letters. 13: 2984-7. PMID 21612194 DOI: 10.1021/Ol200696Q |
0.599 |
|
2011 |
Croatt MP, Carreira EM. Probing the role of the mycosamine C2'-OH on the activity of amphotericin B. Organic Letters. 13: 1390-3. PMID 21322610 DOI: 10.1021/Ol2000765 |
0.44 |
|
2010 |
Croatt MP, Wender PA. The diene effect: The design, development, and Mechanistic investigation of metal-catalyzed diene-yne, diene-ene, and diene-allene [2+2+1] cycloaddition reactions European Journal of Organic Chemistry. 19-32. DOI: 10.1002/Ejoc.200900929 |
0.703 |
|
2009 |
Wender PA, Croatt MP, Kühn B. Rhodium(I)-catalyzed [2+2], [2+2+2], and [2+2+2+2] cycloadditions of dienes or alkynes with a bis-ene Organometallics. 28: 5841-5844. DOI: 10.1021/Om9007373 |
0.698 |
|
2007 |
Wender PA, Croatt MP, Deschamps NM. C-C bond formation (part 1) by addition reactions: Higher-order cycloadditions Comprehensive Organometallic Chemistry Iii. 10: 603-647. |
0.678 |
|
2006 |
Wender PA, Croatt MP, Deschamps NM. Metal-catalyzed [2+2+1] cycloadditions of 1,3-dienes, allenes, and CO. Angewandte Chemie (International Ed. in English). 45: 2459-62. PMID 16526073 DOI: 10.1002/Anie.200600300 |
0.707 |
|
2006 |
Wender PA, Croatt MP, Witulski B. New reactions and step economy: the total synthesis of (±)-salsolene oxide based on the type II transition metal-catalyzed intramolecular [4+4] cycloaddition Tetrahedron. 62: 7505-7511. DOI: 10.1016/J.Tet.2006.02.085 |
0.594 |
|
2004 |
Wender PA, Croatt MP, Deschamps NM. Rhodium(I)-catalyzed [2+2+1] cycloadditions of 1,3-dienes, alkenes, and CO. Journal of the American Chemical Society. 126: 5948-9. PMID 15137743 DOI: 10.1021/Ja0489487 |
0.701 |
|
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