| Year |
Citation |
Score |
| 2020 |
Mohan RS, Mejia MP. Environmentally Friendly Organic Chemistry Laboratory Experiments for the Undergraduate Curriculum: A Literature Survey and Assessment Journal of Chemical Education. 97: 943-959. DOI: 10.1021/Acs.Jchemed.9B00753 |
0.325 |
|
| 2015 |
Yoo JS, Laughlin TJ, Krob JJ, Mohan RS. Bismuth(III) bromide catalyzed synthesis of polyhydroquinoline derivatives via the Hantzsch reaction Tetrahedron Letters. DOI: 10.1016/J.Tetlet.2015.04.121 |
0.486 |
|
| 2013 |
Starcevich JT, Laughlin TJ, Mohan RS. Iron(III) tosylate catalyzed synthesis of 3,4-dihydropyrimidin-2(1H)-ones/ thiones via the Biginelli reaction Tetrahedron Letters. 54: 983-985. DOI: 10.1016/J.Tetlet.2012.12.032 |
0.486 |
|
| 2012 |
Krabbe SW, Mohan RS. Environmentally friendly organic synthesis using bismuth(III) compounds. Topics in Current Chemistry. 311: 45-68. PMID 21837557 DOI: 10.1007/128_2011_194 |
0.424 |
|
| 2012 |
Baldwin NJ, Nord AN, O'Donnell BD, Mohan RS. Iron(III) tosylate catalyzed acylation of alcohols, phenols, and aldehydes Tetrahedron Letters. 53: 6946-6949. DOI: 10.1016/J.Tetlet.2012.10.033 |
0.397 |
|
| 2011 |
Bothwell JM, Krabbe SW, Mohan RS. Applications of bismuth(III) compounds in organic synthesis. Chemical Society Reviews. 40: 4649-707. PMID 21589974 DOI: 10.1039/C0Cs00206B |
0.407 |
|
| 2011 |
Bothwell JM, Krabbe SW, Mohan RS. Applications of bismuth(iii) compounds in organic synthesis Chemical Society Reviews. 40: 4649-4707. DOI: 10.1039/c0cs00206b |
0.309 |
|
| 2011 |
Bockman MR, Angeles VV, Martino JM, Vagadia PP, Mohan RS. A mild method for the deprotection of tetrahydropyranyl (THP) ethers catalyzed by iron(III) tosylate Tetrahedron Letters. 52: 6939-6941. DOI: 10.1016/J.Tetlet.2011.10.068 |
0.364 |
|
| 2010 |
Krabbe SW, Spafford MJ, Mohan RS. Bismuth(III) Triflate Catalyzed Allylation of Cyclic Acetals and Dithianes Followed byin situDerivatization to Generate Highly Functionalized Esters Organic Preparations and Procedures International. 42: 363-371. DOI: 10.1080/00304948.2010.495652 |
0.384 |
|
| 2010 |
Podgorski DM, Krabbe SW, Le LN, Sierszulski PR, Mohan RS. Bismuth Compounds in Organic Synthesis: Synthesis of Dioxanes, Dioxepines, and Dioxolanes Catalyzed by Bismuth(III) Triflate Synthesis. 2010: 2771-2775. DOI: 10.1055/S-0030-1258148 |
0.478 |
|
| 2010 |
Krabbe SW, Angeles VV, Mohan RS. Bismuth(III) bromide in organic synthesis. A catalytic method for the allylation of tetrahydrofuranyl and tetrahydropyranyl ethers Tetrahedron Letters. 51: 5643-5645. DOI: 10.1016/J.Tetlet.2010.08.079 |
0.504 |
|
| 2010 |
Olson ME, Carolan JP, Chiodo MV, Lazzara PR, Mohan RS. Iron(III) tosylate-catalyzed deprotection of aromatic acetals in water Tetrahedron Letters. 51: 3969-3971. DOI: 10.1016/J.Tetlet.2010.05.112 |
0.365 |
|
| 2010 |
Bothwell JM, Angeles VV, Carolan JP, Olson ME, Mohan RS. Erratum to “A mild and chemoselective method for the deprotection of tert-butyldimethylsilyl (TBDMS) ethers using iron(III) tosylate as a catalyst” [Tetrahedron Lett. 51 (2010) 1056–1058] Tetrahedron Letters. 51: 3696. DOI: 10.1016/J.Tetlet.2010.05.047 |
0.353 |
|
| 2010 |
Bothwell JM, Angeles VV, Carolan JP, Olson ME, Mohan RS. A mild and chemoselective method for the deprotection of tert-butyldimethylsilyl (TBDMS) ethers using iron(III) tosylate as a catalyst Tetrahedron Letters. 51: 1056-1058. DOI: 10.1016/J.Tetlet.2009.12.076 |
0.384 |
|
| 2009 |
Rogers JL, Ernat JJ, Yung H, Mohan RS. Environmentally friendly organic synthesis using bismuth compounds. Bismuth(III) bromide catalyzed synthesis of substituted tetrahydroquinoline derivatives Catalysis Communications. 10: 625-626. DOI: 10.1016/J.Catcom.2008.11.004 |
0.5 |
|
| 2008 |
Spafford MJ, Christensen JE, Huddle MG, Lacey JR, Mohan RS. Environmentally friendly organic synthesis using bismuth compounds. bismuth trifluoromethanesulfonate-catalyzed allylation of dioxolanes Australian Journal of Chemistry. 61: 419-421. DOI: 10.1071/Ch08109 |
0.503 |
|
| 2008 |
Giarrusso MA, Higham LT, Kreher UP, Mohan RS, Rosamilia AE, Scott JL, Strauss CR. Platform technology for dienone and phenol-formaldehyde architectures Green Chemistry. 10: 842-852. DOI: 10.1039/B802755B |
0.351 |
|
| 2008 |
Christensen JE, Huddle MG, Rogers JL, Yung H, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 7. Rearrangement of trans-Stilbene Oxide with Bismuth Trifluoromethanesulfonate and Other Metal Triflates. A Microscale Green Organic Chemistry Laboratory Experiment Journal of Chemical Education. 85: 1274. DOI: 10.1021/Ed085P1274 |
0.407 |
|
| 2008 |
Bailey AD, Baru AR, Tasche KK, Mohan RS. Environmentally friendly organic synthesis using bismuth compounds: bismuth(III) iodide catalyzed deprotection of acetals in water Tetrahedron Letters. 49: 691-694. DOI: 10.1016/J.Tetlet.2007.11.127 |
0.425 |
|
| 2007 |
Spafford MJ, Anderson ED, Lacey JR, Palma AC, Mohan RS. Iron(III) p-toluenesulfonate catalyzed synthesis of homoallyl ethers from acetals and aldehydes Tetrahedron Letters. 48: 8665-8667. DOI: 10.1016/J.Tetlet.2007.10.026 |
0.438 |
|
| 2006 |
Olivero S, Perriot R, Duñach E, Baru AR, Bell ED, Mohan RS. An environmentally friendly synthesis of functionalized indanes using electrochemical cyclization of ortho-halo-substituted homoallyl ethers and esters Synlett. 2021-2026. DOI: 10.1055/S-2006-948182 |
0.46 |
|
| 2006 |
Bailey AD, Cherney SM, Anzalone PW, Anderson ED, Ernat JJ, Mohan RS. A Convenient Method for in situ Generation of I2 Using CuSO4/NaI and Its Applications to the Deprotection of Acetals, Etherifications and Iodolactonizations. Cheminform. 37. DOI: 10.1055/S-2005-923586 |
0.316 |
|
| 2005 |
Anzalone PW, Baru AR, Danielson EM, Hayes PD, Nguyen MP, Panico AF, Smith RC, Mohan RS. Bismuth compounds in organic synthesis. A one-pot synthesis of homoallyl ethers and homoallyl acetates from aldehydes catalyzed by bismuth triflate. The Journal of Organic Chemistry. 70: 2091-6. PMID 15760192 DOI: 10.1021/Jo048475M |
0.524 |
|
| 2005 |
Ukachukwu VC, Mohan RS, Whalen DL. Kinetic deuterium isotope effects on the reactions of 4-methoxystyrene oxide in water solution Arkivoc. 2006. DOI: 10.3998/Ark.5550190.0007.305 |
0.316 |
|
| 2005 |
Anzalone PW, Mohan RS. Trimethylsilyl trifluoromethanesulfonate catalyzed one-pot method for the conversion of aldehydes to homoallyl ethers in an ionic liquid Synthesis. 2005: 2661-2663. DOI: 10.1055/S-2005-872112 |
0.437 |
|
| 2005 |
Baru AR, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 6. Selective Reduction in Organic Chemistry: Reduction of Aldehydes in the Presence of Esters Using Sodium Borohydride Journal of Chemical Education. 82: 1674-1675. DOI: 10.1021/Ed082P1674 |
0.412 |
|
| 2005 |
Lacey JR, Anzalone PW, Duncan CM, Hackert MJ, Mohan RS. A study of epoxyolefin cyclizations catalyzed by bismuth trifluoromethanesulfonate and other metal triflates Tetrahedron Letters. 46: 8507-8511. DOI: 10.1016/J.Tetlet.2005.10.013 |
0.356 |
|
| 2005 |
Anderson ED, Ernat JJ, Nguyen MP, Palma AC, Mohan RS. Environment friendly organic synthesis using bismuth compounds. An efficient method for carbonyl-ene reactions catalyzed by bismuth triflate Tetrahedron Letters. 46: 7747-7750. DOI: 10.1016/J.Tetlet.2005.09.035 |
0.505 |
|
| 2004 |
Mohan R, Nattier B, Eash K. Deprotection of Ketoximes Using Bismuth(III) Nitrate Pentahydrate Synthesis. 2001. DOI: 10.1055/S-2001-14568 |
0.358 |
|
| 2004 |
Nguyen MP, Arnold JN, Peterson KE, Mohan RS. Environment-friendly organic synthesis using bismuth compounds. Bismuth triflate catalyzed synthesis of substituted 3,4-dihydro-2H-1-benzopyrans Tetrahedron Letters. 45: 9369-9371. DOI: 10.1016/J.Tetlet.2004.10.118 |
0.452 |
|
| 2004 |
Aggen DH, Arnold JN, Hayes PD, Smoter NJ, Mohan RS. Bismuth compounds in organic synthesis. Bismuth nitrate catalyzed chemoselective synthesis of acylals from aromatic aldehydes Tetrahedron. 60: 3675-3679. DOI: 10.1016/j.tet.2004.02.046 |
0.417 |
|
| 2004 |
Aggen DH, Arnold JN, Hayes PD, Smoter NJ, Mohan RS. Bismuth Compounds in Organic Synthesis. Bismuth Nitrate Catalyzed Chemoselective Synthesis of Acylals from Aromatic Aldehydes. Cheminform. 35. DOI: 10.1016/J.Tet.2004.02.046 |
0.511 |
|
| 2003 |
Zerth HM, Leonard NM, Mohan RS. Synthesis of homoallyl ethers via allylation of acetals in ionic liquids catalyzed by trimethylsilyl trifluoromethanesulfonate. Organic Letters. 5: 55-7. PMID 12509889 DOI: 10.1021/Ol0271739 |
0.427 |
|
| 2003 |
Arnold JN, Hayes PD, Kohaus RL, Mohan RS. Bismuth compounds in organic synthesis. Deprotection of ketoximes using bismuth bromide-bismuth triflate Tetrahedron Letters. 44: 105-107. DOI: 10.1016/J.Tetlet.2003.10.031 |
0.418 |
|
| 2003 |
Peterson KE, Smith RC, Mohan RS. Bismuth compounds in organic synthesis. Synthesis of resorcinarenes using bismuth triflate Tetrahedron Letters. 44: 7723-7725. DOI: 10.1016/J.Tetlet.2003.08.093 |
0.48 |
|
| 2003 |
Stephens J, Butler P, Clow C, Oswald M, Smith R, Mohan R. Bismuth Triflate: An Efficient Catalyst for the Formation and Deprotection of Tetrahydropyranyl Ethers European Journal of Organic Chemistry. 2003: 3827-3831. DOI: 10.1002/Ejoc.200300295 |
0.395 |
|
| 2002 |
Leonard NM, Oswald MC, Freiberg DA, Nattier BA, Smith RC, Mohan RS. A simple and versatile method for the synthesis of acetals from aldehydes and ketones using bismuth triflate. The Journal of Organic Chemistry. 67: 5202-7. PMID 12126407 DOI: 10.1021/Jo0258249 |
0.477 |
|
| 2002 |
Carrigan MD, Sarapa D, Smith RC, Wieland LC, Mohan RS. A simple and efficient chemoselective method for the catalytic deprotection of acetals and ketals using bismuth triflate. The Journal of Organic Chemistry. 67: 1027-30. PMID 11856058 DOI: 10.1021/Jo016180S |
0.481 |
|
| 2002 |
Wieland LC, Zerth HM, Mohan RS. Bismuth triflate catalyzed allylation of acetals: A simple and mild method for synthesis of homoallyl ethers Tetrahedron Letters. 43: 4597-4600. DOI: 10.1016/S0040-4039(02)00906-1 |
0.483 |
|
| 2002 |
Leonard NM, Wieland LC, Mohan RS. Applications of bismuth(III) compounds in organic synthesis Tetrahedron. 58: 8373-8397. DOI: 10.1016/S0040-4020(02)01000-1 |
0.381 |
|
| 2001 |
Cabay ME, Ettlie BJ, Tuite AJ, Welday KA, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 5. Stereochemistry of E2 Elimination: Elimination of cis- and trans-2-Methylcyclohexyl Tosylate Journal of Chemical Education. 78: 79. DOI: 10.1021/Ed078P79 |
0.359 |
|
| 2001 |
Centko RS, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 4. Epoxidation of p-Methoxy-trans-β[beta]-methylstyrene: An Exercise in NMR and IR Spectroscopy for Sophomore Organic Laboratories Journal of Chemical Education. 78: 77. DOI: 10.1021/Ed078P77 |
0.397 |
|
| 2001 |
Carrigan MD, Eash KJ, Oswald MC, Mohan RS. An efficient method for the chemoselective synthesis of acylals from aromatic aldehydes using bismuth triflate Tetrahedron Letters. 42: 8133-8135. DOI: 10.1016/S0040-4039(01)01756-7 |
0.483 |
|
| 2001 |
Bhatia KA, Eash KJ, Leonard NM, Oswald MC, Mohan RS. A facile and efficient method for the rearrangement of aryl-substituted epoxides to aldehydes and ketones using bismuth triflate Tetrahedron Letters. 42: 8129-8132. DOI: 10.1016/S0040-4039(01)01519-2 |
0.431 |
|
| 2000 |
Eash KJ, Pulia MS, Wieland LC, Mohan RS. A simple chemoselective method for the deprotection of acetals and ketals using bismuth nitrate pentahydrate The Journal of Organic Chemistry. 65: 8399-401. PMID 11101407 DOI: 10.1021/Jo001202G |
0.347 |
|
| 2000 |
Mohan RS, Gavardinas K, Kyere S, Whalen DL. Spontaneous hydrolysis reactions of cis- and trans-beta-methyl-4-methoxystyrene oxides (Anethole oxides): buildup of trans-anethole oxide as an intermediate in the spontaneous reaction of cis-anethole oxide. The Journal of Organic Chemistry. 65: 1407-13. PMID 10814102 DOI: 10.1021/Jo991521B |
0.368 |
|
| 2000 |
Monk KA, Sarapa D, Mohan RS. Bismuth (III) Acetate: A New Catalyst for Preparation of Azlactones via the Erlenmeyer Synthesis Synthetic Communications. 30: 3167-3170. DOI: 10.1080/00397910008086926 |
0.458 |
|
| 2000 |
Sgariglia EA, Schopp R, Gavardinas K, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 3. Rearrangement of cis- and trans-Stilbene Oxides with Boron Trifluoride Etherate. An Exercise in 1H NMR Spectroscopy for Sophomore Organic Laboratories Journal of Chemical Education. 77: 79. DOI: 10.1021/Ed077P79 |
0.412 |
|
| 2000 |
Anderson AM, Blazek JM, Garg P, Payne BJ, Mohan RS. Bismuth(III) oxide perchlorate promoted rearrangement of epoxides to aldehydes and ketones Tetrahedron Letters. 41: 1527-1530. DOI: 10.1016/S0040-4039(99)02330-8 |
0.398 |
|
| 1999 |
McElveen SR, Gavardinas K, Stamberger JA, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 1. Nitration of Unknown Organic Compounds. An Exercise in 1H NMR and 13C NMR Spectrosopy for Sophomore Organic Laboratories Journal of Chemical Education. 76: 535-535. DOI: 10.1021/Ed076P535 |
0.326 |
|
| 1999 |
Monk KA, Mohan RS. The Hofmann rearrangement using household bleach: Synthesis of 3-nitroaniline Journal of Chemical Education. 76: 1717. DOI: 10.1021/Ed076P1717 |
0.454 |
|
| 1999 |
Shadwick SR, Mohan RS. The Discovery-Oriented Approach to Organic Chemistry. 2. Selectivity in Alcohol Oxidation. An Exercise in 1H NMR Spectroscopy for Sophomore Organic Laboratories Journal of Chemical Education. 76: 1121-1122. DOI: 10.1021/Ed076P1121 |
0.347 |
|
| 1999 |
Tymonko SA, Nattier BA, Mohan RS. Oxidation of benzoins to benzils using bismuth(III) nitrate-copper(II) acetate Tetrahedron Letters. 40: 7657-7659. DOI: 10.1016/S0040-4039(99)01583-X |
0.334 |
|
| 1994 |
Shipley DS, Ross AM, Mohan RS, Whalen DL, Sayer JM, Serve PM, Jerina DM. Solvolysis of (4-Nitrophenoxy)ethylene Oxides The Journal of Organic Chemistry. 59: 977-983. DOI: 10.1021/Jo00084A012 |
0.309 |
|
| 1993 |
Mohan RS, Whalen DL. Acid-catalyzed hydrolysis of cis- and trans-anethole oxides: discrete carbocation intermediates and syn/anti hydration ratios The Journal of Organic Chemistry. 58: 2663-2669. DOI: 10.1021/Jo00062A006 |
0.324 |
|
| 1993 |
Blumenstein JJ, Ukachukwu VC, Mohan RS, Whalen DL. Effects of para-substituents on the mechanisms of solvolysis of styrene oxides The Journal of Organic Chemistry. 58: 924-932. DOI: 10.1021/Jo00056A027 |
0.321 |
|
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