| Year |
Citation |
Score |
| 2019 |
Kadoya WM, Sierra-Alvarez R, Jagadish B, Wong S, Abrell L, Mash EA, Field JA. Coupling reactions between reduced intermediates of insensitive munitions compound analog 4-nitroanisole. Chemosphere. 222: 789-796. PMID 30739063 DOI: 10.1016/J.Chemosphere.2019.01.163 |
0.311 |
|
| 2017 |
Kadoya WM, Sierra-Alvarez R, Wong S, Abrell L, Mash EA, Field JA. Evidence of anaerobic coupling reactions between reduced intermediates of 4-nitroanisole. Chemosphere. 195: 372-380. PMID 29274576 DOI: 10.1016/J.Chemosphere.2017.12.083 |
0.307 |
|
| 2017 |
Jagadish B, Hurley NR, Mash EA. Solvent-free nitration of electron-rich arenes Synthetic Communications. 47: 2395-2398. DOI: 10.1080/00397911.2017.1378682 |
0.325 |
|
| 2015 |
Dehigaspitiya DC, Anglin BL, Smith KR, Weber CS, Lynch RM, Mash EA. Linear scaffolds for multivalent targeting of melanocortin receptors. Organic & Biomolecular Chemistry. PMID 26461460 DOI: 10.1039/C5Ob01779C |
0.757 |
|
| 2015 |
Dehigaspitiya DC, Navath S, Weber CS, Lynch RM, Mash EA. Synthesis and bioactivity of MSH4 oligomers prepared by an A2 + B2 strategy. Tetrahedron Letters. 56: 3060-3065. PMID 26120211 DOI: 10.1016/J.Tetlet.2014.12.022 |
0.771 |
|
| 2014 |
Jagadish B, Ozumerzifon TJ, Roberts SA, Hall GB, Mash EA, Raghunand N. IMPROVED SYNTHESIS OF 10-(2-ALKYLAMINO-2-OXOETHYL)-1,4,7,10-TETRAAZACYCLODODECANE-1,4,7-TRIACETIC ACID DERIVATIVES BEARING ACID-SENSITIVE LINKERS. Synthetic Communications. 44. PMID 24363464 DOI: 10.1080/00397911.2013.813547 |
0.34 |
|
| 2013 |
Alleti R, Vagner J, Dehigaspitiya DC, Moberg VE, Elshan NG, Tafreshi NK, Brabez N, Weber CS, Lynch RM, Hruby VJ, Gillies RJ, Morse DL, Mash EA. Synthesis and characterization of time-resolved fluorescence probes for evaluation of competitive binding to melanocortin receptors. Bioorganic & Medicinal Chemistry. 21: 5029-38. PMID 23890524 DOI: 10.1016/J.Bmc.2013.06.052 |
0.753 |
|
| 2012 |
Wells KE, Weatherhead RA, Murigi FN, Nichol GS, Carducci MD, Selby HD, Mash EA. Organic crystal engineering with 1,4-piperazine-2,5-diones. 8. Synthesis, crystal packing, and thermochemistry of piperazinediones derived from 2-amino-4,7-dialkoxyindan-2-carboxylic acids Crystal Growth and Design. 12: 5056-5068. DOI: 10.1021/Cg301003P |
0.31 |
|
| 2011 |
Jagadish B, Brickert-Albrecht GL, Nichol GS, Mash EA, Raghunand N. On the Synthesis of 1,4,7-Tris(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane. Tetrahedron Letters. 52: 2058-2061. PMID 21516221 DOI: 10.1016/J.Tetlet.2010.10.074 |
0.327 |
|
| 2010 |
Nichol GS, Murigi FN, Mash EA. A synchrotron study of (2R,5'S)-5'-benzyl-5-bromo-6-methoxyspiro[indane-2,2'-piperazine]-3',6'-dione dimethylformamide solvate. Acta Crystallographica. Section C, Crystal Structure Communications. 66: o302-4. PMID 20522950 DOI: 10.1107/S0108270110017579 |
0.313 |
|
| 2010 |
Murigi FN, Nichol GS, Mash EA. Synthesis of the conformationally constrained tyrosine analogues, (R)- and (S)-5-hydroxy-2-aminoindan-2-carboxylic acids. The Journal of Organic Chemistry. 75: 1293-6. PMID 20095557 DOI: 10.1021/Jo902438S |
0.357 |
|
| 2010 |
MASH EA, GREGG TM, BARON JA. ChemInform Abstract: Diastereoselective Manipulations of Bicyclo[m.1.0]alkane Derivatives. Part 4. Reactions of Nucleophiles with Bicyclo[m.1.0]alk-3-en-2-ones. Cheminform. 29: no-no. DOI: 10.1002/chin.199828091 |
0.685 |
|
| 2010 |
WALLER SC, MASH EA. ChemInform Abstract: Improved Synthesis of 2,2′,3,3′,6,6′-Hexachlorobiphenyl. Cheminform. 29: no-no. DOI: 10.1002/chin.199810103 |
0.714 |
|
| 2010 |
MASH EA, GREGG TM, KACZYNSKI MA. ChemInform Abstract: Diastereoselective Manipulations of Bicyclo(m.1.0)alkane Derivatives. Part 2. Nucleophilic Additions to the Carbonyl Carbons of Bicyclo(m.1. 0)alkan-2-ones. Cheminform. 27: no-no. DOI: 10.1002/chin.199634091 |
0.687 |
|
| 2010 |
MASH EA, NIMKAR SK, DEMOSS SM. ChemInform Abstract: A Synthesis of the 4-Alkylamino-2,4-dideoxy-L-threo-pentopyranose Components of the Calicheamicins and Esperamicins. Cheminform. 27: no-no. DOI: 10.1002/chin.199614247 |
0.785 |
|
| 2009 |
Weatherhead RA, Carducci MD, Mash EA. Synthesis of conformationally constrained diaminodicarboxylic acid derivatives. The Journal of Organic Chemistry. 74: 8773-8. PMID 19848385 DOI: 10.1021/Jo901892D |
0.332 |
|
| 2008 |
Hammaker JR, Mash EA. NOTE: Synthesis and characterization of a poly(acrylamide) with pendant 1,4-piperazine-2,5-dione moieties via post-polymerization cyclization Journal of Macromolecular Science, Part a: Pure and Applied Chemistry. 45: 865-871. DOI: 10.1080/10601320802300842 |
0.313 |
|
| 2008 |
Ntirampebura D, Jagadish B, Nichol GS, Carducci MD, Dawson A, Rajapakshe A, Oliver AG, Clegg W, Harrington RW, Layne L, Margolis JI, Mash EA. Organic crystal engineering with 1,4-piperazine-2,5-diones. 7. Crystal packing of piperazinediones derived from 2-amino-7-nitro-4-methoxyindan-2- carboxylic acid Crystal Growth and Design. 8: 3257-3270. DOI: 10.1021/Cg701240M |
0.322 |
|
| 2006 |
Aavula BR, Ali MA, Mash EA, Bednarczyk D, Wright SH. Synthesis and Fluorescence of N,N,N‐Trimethyl‐2‐[methyl(7‐nitrobenzo[c][l,2,5]oxadiazol‐4‐yl) amino]ethanaminium Iodide, a pH‐Insensitive Reporter of Organic Cation Transport Synthetic Communications. 36: 701-705. DOI: 10.1080/00397910500446597 |
0.333 |
|
| 2005 |
Jones IW, Monguchi Y, Dawson A, Carducci MD, Mash EA. Synthesis of 1,10-dimethylbicyclo[8.8.8]hexacosane and 1,10-dihydroxybicyclo[8.8.8]hexacosane. Organic Letters. 7: 2841-3. PMID 15987150 DOI: 10.1021/Ol050714K |
0.35 |
|
| 2005 |
Monguchi Y, Vagner J, Handl HL, Jana U, Begay LJ, Hruby VJ, Gillies RJ, Mash EA. Design, synthesis, and validation of rigid linkers for bioactive peptides Tetrahedron Letters. 46: 7589-7592. DOI: 10.1016/J.Tetlet.2005.08.151 |
0.315 |
|
| 2005 |
Jagadish B, Iyengar BS, Sólyom AM, Remers WA, Dorr RT, Yu JS, Gupta S, Mash EA. Synthesis of [14C]-imexon Journal of Labelled Compounds and Radiopharmaceuticals. 48: 165-170. DOI: 10.1002/Jlcr.911 |
0.305 |
|
| 2003 |
Kloster RA, Carducci MD, Mash EA. Crystal engineering of a liquid crystalline piperazinedione. Organic Letters. 5: 3683-6. PMID 14507204 DOI: 10.1021/Ol035365D |
0.754 |
|
| 2003 |
Jagadish B, Carducci MD, Bosshard C, Günter P, Margolis JI, Williams LJ, Mash EA. Organic crystal engineering with piperazine-2,5-diones. 4. Crystal packing of piperazinediones derived from 2-amino-7-cyano-4-methoxyindan-2-carboxylic acid Crystal Growth and Design. 3: 811-821. DOI: 10.1021/Cg0340751 |
0.552 |
|
| 2003 |
Jagadish B, Aposhian HV, Mash EA. An efficient synthesis of sodium dimethylarsinate-14C Journal of Labelled Compounds and Radiopharmaceuticals. 46: 373-377. DOI: 10.1002/Jlcr.667 |
0.314 |
|
| 2003 |
Mash EA, Nelson KA, Deusen SV, Hemperly SB. 1,4-Di-O-Alkyl Threitols from Tartaric Acid: 1,4-Di-O-Benzyl-L-Threitol Organic Syntheses. 92-92. DOI: 10.1002/0471264180.Os068.12 |
0.771 |
|
| 2002 |
Li Y, Carter DE, Mash EA. Synthesis and structure of the glutathione conjugate of chloroacetaldehyde Synthetic Communications. 32: 1579-1583. DOI: 10.1081/Scc-120004149 |
0.399 |
|
| 2000 |
Mash EA, Aavula BR. Synthesis of 7-alkoxyquinolines, coumarins, and resorufins Synthetic Communications. 30: 367-375. DOI: 10.1080/00397910008087329 |
0.38 |
|
| 2000 |
Aavula BR, Cui Q, Mash EA. Synthesis of (S)-(-)-β-cuparenone and (S)-(-)-cuparene Tetrahedron Asymmetry. 11: 4681-4686. DOI: 10.1016/S0957-4166(00)00457-2 |
0.378 |
|
| 2000 |
Jagadish B, Williams LJ, Carducci MD, Bosshard C, Mash EA. The crystal packing of a strongly dipolar piperazinedione Tetrahedron Letters. 41: 9483-9487. DOI: 10.1016/S0040-4039(00)01623-3 |
0.528 |
|
| 2000 |
Nimkar KS, Mash EA. Intermolecular and intramolecular reactions of resolved 2-alkoxytetrahydrofuran-3-yl and 2-alkoxytetrahydropyran-3-yl radicals Tetrahedron. 56: 5793-5800. DOI: 10.1016/S0040-4020(00)00547-0 |
0.776 |
|
| 1999 |
Waller SC, He YA, Harlow GR, He YQ, Mash EA, Halpert JR. 2,2',3,3',6,6'-hexachlorobiphenyl hydroxylation by active site mutants of cytochrome P450 2B1 and 2B11. Chemical Research in Toxicology. 12: 690-9. PMID 10458702 DOI: 10.1021/Tx990030J |
0.685 |
|
| 1999 |
Mash EA, Baron JA. Diastereoselective manipulations of bicyclo[m.1.0]alkane derivatives. 6. Stereocontrolled synthesis of tricyclo[m.n.0.0]alkenones Journal of Organic Chemistry. 64: 7412-7418. DOI: 10.1021/Jo990720S |
0.395 |
|
| 1999 |
Williams LJ, Jagadish B, Lyon SR, Kloster RA, Carducci MD, Mash EA. Organic crystal engineering with piperazine-2,5-diones. 1. Crystal packing of piperazinediones derived from substituted 2-aminoindan-2- carboxylic acids Tetrahedron. 55: 14281-14300. DOI: 10.1016/S0040-4020(99)00925-4 |
0.765 |
|
| 1999 |
Williams LJ, Jagadish B, Lansdown MG, Carducci MD, Mash EA. Organic crystal engineering with piperazine-2,5-diones. 2. Crystal packing of weakly dipolar piperazinediones derived from 2-amino-4-bromo-7- methoxyindan-2-carboxylic acid Tetrahedron. 55: 14301-14322. DOI: 10.1016/S0040-4020(99)00924-2 |
0.558 |
|
| 1998 |
Kawabe Y, Spiegelberg C, Schülzgen A, Nabor MF, Jabbour GE, Kippelen B, Mash EA, Allemand PM, Peyghambarian N, Kuwata-Gonokami M, Takeda K. Whispering-gallery-mode oscillation in a polymer microring laser Proceedings of Spie - the International Society For Optical Engineering. 3281: 211-216. DOI: 10.1117/12.305423 |
0.751 |
|
| 1998 |
Li Y, Carter DE, Mash EA. Synthesis of the mono-cysteine disulfide of meso-2,3-dimercaptosuccinic acid Synthetic Communications. 28: 2057-2062. DOI: 10.1080/00397919808007181 |
0.393 |
|
| 1998 |
Shaheen SE, Jabbour GE, Morrell MM, Kawabe Y, Kippelen B, Peyghambarian N, Nabor MF, Schlaf R, Mash EA, Armstrong NR. Bright blue organic light-emitting diode with improved color purity using a LiF/Al cathode Journal of Applied Physics. 84: 2324-2327. DOI: 10.1063/1.368299 |
0.757 |
|
| 1998 |
Schülzgen A, Spiegelberg C, Morrell MM, Mendes SB, Kippelen B, Peyghambarian N, Nabor MF, Mash EA, Allemand PM. Near diffraction-limited laser emission from a polymer in a high finesse planar cavity Applied Physics Letters. 72: 269-271. DOI: 10.1063/1.120709 |
0.754 |
|
| 1998 |
Kawabe Y, Spiegelberg C, Schülzgen A, Nabor MF, Kippelen B, Mash EA, Allemand PM, Kuwata-Gonokami M, Takeda K, Peyghambarian N. Whispering-gallery-mode microring laser using a conjugated polymer Applied Physics Letters. 72: 141-143. DOI: 10.1063/1.120668 |
0.753 |
|
| 1998 |
Mash EA, Baron JA, Gregg TM, Nimkar SK. Diastereoselective manipulations of bicyclo[m.1.0]alkane derivatives. 5. α'-Alkylations of bicycle[m.1.0]alkan-2-ones Tetrahedron. 54: 2669-2682. DOI: 10.1016/S0040-4020(98)83003-2 |
0.785 |
|
| 1998 |
Schulzgen A, Spiegelberg C, Morrell MM, Mendes SB, Nabor MF, Mash EA, Allemand PM, Kippelen B. Vertical-cavity surface-emitting polymer laser Conference On Lasers and Electro-Optics Europe - Technical Digest. 6-7. |
0.748 |
|
| 1997 |
Mash EA, Gregg TM, Baron JA. Diastereoselective Manipulations of Bicyclo[m.1.0]alkane Derivatives. 4. Reactions of Nucleophiles with Bicyclo[m.1.0]alk-3-en-2-ones. The Journal of Organic Chemistry. 62: 8513-8521. PMID 11671994 DOI: 10.1021/Jo971359H |
0.721 |
|
| 1997 |
Mash EA, Kantor LTA, Waller SC. Monobenzylation of 1,n-diols via dibutylstannylene intermediates Synthetic Communications. 27: 507-514. DOI: 10.1080/00397919708006052 |
0.686 |
|
| 1997 |
Waller SC, Mash EA. Improved syntheses of 2,2',3,3',6,6'-hexachlorobiphenyl Organic Preparations and Procedures International. 29: 679-685. DOI: 10.1080/00304949709355248 |
0.693 |
|
| 1997 |
Mash EA, Williams LJ, Pfeiffer SS. Synthesis of ethyl N-(diphenyl)methyl-1,2,3,4- tetrahydroisoquinoline-3-carboxylates Tetrahedron Letters. 38: 6977-6980. DOI: 10.1016/S0040-4039(97)01668-7 |
0.612 |
|
| 1997 |
Mash EA, Nimkar KS, Baron JA. Diastereoselective manipulations of bicyclo[m.1.0] alkane derivatives. 3. Nucleophilic additions to the carbonyl carbon of (1R,8R)-Bicyclo[6.1.0]nonan-2,6-dione 2-(2S,3S)-1,4-Di-O-methyl-1,2,3,4-butane ketal Tetrahedron. 53: 9043-9056. DOI: 10.1016/S0040-4020(97)00615-7 |
0.789 |
|
| 1997 |
Mash EA, Gregg TM, Stahl MT. Development of Molecular Mechanics Torsion Parameters for α,β-Cyclopropyl α′,β′-Enones and Conformational Analysis of Bicyclo[m.1.0]alk-3-en-2-ones Journal of Organic Chemistry. 62: 3715-3721. |
0.767 |
|
| 1996 |
Mash EA, Gregg TM, Kaczynski MA. Diastereoselective Manipulations of Bicyclo[m.1.0]alkane Derivatives. 2. Nucleophilic Additions to the Carbonyl Carbons of Bicyclo[m.1.0]alkan-2-ones(1). The Journal of Organic Chemistry. 61: 2743-2752. PMID 11667108 DOI: 10.1021/Jo951753K |
0.727 |
|
| 1996 |
Mash EA, Gregg TM, Stahl MT, Walters WP. Development of Molecular Mechanics Torsion Parameters for alpha,beta-Cyclopropyl Ketones and Conformational Analysis of Bicyclo[m.1.0]alkan-2-ones. The Journal of Organic Chemistry. 61: 2738-2742. PMID 11667107 DOI: 10.1021/Jo951752S |
0.775 |
|
| 1996 |
Mash EA, Waller SC. Syntheses and spectroscopic characterizations of oxidative metabolites of 4-vinylcyclohexene II diol-epoxides Toxicological and Environmental Chemistry. 57: 153-162. DOI: 10.1080/02772249609358384 |
0.692 |
|
| 1996 |
Mash EA, Gregg TM, Kaczynski MA. Diastereoselective manipulations of bicyclo[m.1.0]alkane derivatives. 2. Nucleophilic additions to the carbonyl carbons of bicyclot[m.1.0]alkan-2-ones Journal of Organic Chemistry. 61: 2743-2752. |
0.681 |
|
| 1996 |
Mash EA, Gregg TM, Stahl MT, Walters WP. Development of molecular mechanics torsion parameters for α,β-cyclopropyl ketones and conformational analysis of bicyclo[m.1.0]alkan-2-ones Journal of Organic Chemistry. 61: 2738-2742. |
0.77 |
|
| 1995 |
Mash EA, Nimkar SK, DeMoss SM. A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins Journal of Carbohydrate Chemistry. 14: 1369-1378. DOI: 10.1080/07328309508005417 |
0.786 |
|
| 1995 |
Mash EA, Gregg TM. Synthesis of the enantiomers of 4-vinylcyclohexene Journal of Organic Chemistry. 60: 6180-6182. DOI: 10.1021/Jo00124A036 |
0.732 |
|
| 1993 |
Mash EA, Nimkar SK. An efficient stereoconvergent synthesis of the 4-ethylamino-2,4-dideoxy-l-threo-pentopyranose component of the calicheamicins and esperamicins Tetrahedron Letters. 34: 385-388. DOI: 10.1016/0040-4039(93)85082-8 |
0.8 |
|
| 1992 |
Mash EA, Arterburn JB, Nimkar SK. Synthesis of a mevinic acid lactone precursor Journal of Carbohydrate Chemistry. 11: 415-424. DOI: 10.1080/07328309208017803 |
0.799 |
|
| 1991 |
Mash EA, Fryling JA, Wexler PA. Structure of an enantiomerically pure tetrahydropyranyl ether Acta Crystallographica Section C: Crystal Structure Communications. 47: 2708-2709. DOI: 10.1107/S0108270191007953 |
0.773 |
|
| 1991 |
Mash EA, Fryling JA. Enantiomerically pure acetals in organic synthesis. 2. Diastereoselective alkylation of enantiomeric lithio alkyl lactyl tetrahydropyranosides and related enolates Journal of Organic Chemistry. 56: 1094-1098. DOI: 10.1021/Jo00003A035 |
0.812 |
|
| 1991 |
Mash EA, Arterburn JB, Fryling JA, Mitchell SH. Enantiomerically pure acetals in organic synthesis. 1. Chromatographic separability of furanoside and pyranoside acetals derived from .alpha.-hydroxy esters Journal of Organic Chemistry. 56: 1088-1093. DOI: 10.1021/Jo00003A034 |
0.805 |
|
| 1991 |
Mash EA, Arterburn JB. Enantiomerically pure acetals in organic synthesis. 3. A synthesis of (R)-mevalonic acid lactone Journal of Organic Chemistry. 56: 885-888. DOI: 10.1021/Jo00002A079 |
0.656 |
|
| 1991 |
Mash EA, Arterburn JB, Fryling JA, Mitchell SH. Enantiomerically pure acetals in organic synthesis. 1. Chromatographic separability of furanoside and pyranoside acetals derived from α-hydroxy esters Journal of Organic Chemistry. 56: 1088-1093. |
0.801 |
|
| 1990 |
Mash EA, Hemperly SB. Mechanistic studies of diastereoselective cyclopropanation via homochiral ketals. 2. Studies with conformationally restricted 2-cyclohexen-1-one ketals Journal of Organic Chemistry. 55: 2055-2060. DOI: 10.1021/Jo00294A017 |
0.78 |
|
| 1990 |
Mash EA, Hemperly SB, Nelson KA, Heidt PC, Van Deusen S. Mechanistic studies of diastereoselective cyclopropanation via homochiral ketals. 1. Dioxolane structural effects Journal of Organic Chemistry. 55: 2045-2055. DOI: 10.1021/Jo00294A016 |
0.76 |
|
| 1990 |
Mash EA, Kaczynski MA, Dolata DP. Diastereoselective manipulations of conformationally restricted enantiomerically pure bicyclo[m.1.0]alkanes. 1. Nucleophilic additions to the carbonyl carbons of bicyclo[m.1.0]alkan-2-ones Tetrahedron Letters. 31: 4565-4568. DOI: 10.1016/S0040-4039(00)97677-9 |
0.324 |
|
| 1990 |
Kilama JJ, Iyengar BS, Remers WA, Mash EA. A new synthetic approach to the C-D ring portion of streptonigrin analogues Journal of Heterocyclic Chemistry. 27: 1437-1440. DOI: 10.1002/Jhet.5570270547 |
0.376 |
|
| 1989 |
Mash EA, Math SK, Arterburn JB. Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation of medium and large ring α,α-unsaturated ketals derived from 1,4-di-O-benzyl-L-threitol Journal of Organic Chemistry. 54: 4951-4953. DOI: 10.1021/Jo00281A044 |
0.794 |
|
| 1989 |
Mash EA, Torok DS. Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation of α,β-unsaturated ketals derived from (S,S)-(-)-hydrobenzoin Journal of Organic Chemistry. 54: 250-253. DOI: 10.1021/Jo00262A054 |
0.364 |
|
| 1989 |
Mash EA, Arterburn JB, Fryling JA. Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors Tetrahedron Letters. 30: 7145-7148. DOI: 10.1016/S0040-4039(01)93919-X |
0.798 |
|
| 1989 |
Mash EA, Math SK, Flann CJ. Homochiral ketals in organic synthesis. Enantioselective synthesis and absolute configuration of (-)-modhephene Tetrahedron. 45: 4945-4950. DOI: 10.1016/S0040-4020(01)81075-9 |
0.79 |
|
| 1988 |
Mash EA, Math SK. Syntheses and Spectroscopic Characterizations of Oxidative Metabolites of 4-Isopropyibiphenyl Toxicological & Environmental Chemistry. 17: 197-213. DOI: 10.1080/02772248809357290 |
0.76 |
|
| 1988 |
Flann CJ, Mash EA. Homochiral ketals in organic synthesis. enantioselective synthesis of (4S,5S)-4,5-dihydroxycyclopent-2-en-1-one isopropylidine ketal Synthetic Communications. 18: 391-402. DOI: 10.1080/00397918808064002 |
0.78 |
|
| 1988 |
Mash EA, Math SK, Flann CJ. Homochiral ketals in organic synthesis. Enantioselective preparation of (+)-modhephene Tetrahedron Letters. 29: 2147-2150. DOI: 10.1016/S0040-4039(00)86695-2 |
0.799 |
|
| 1988 |
Mash EA, Hemperly SB. Homochiral ketals in organic sythesis. Simple chromatographic resolution of diastereomeric α-hydroxycycloalkanone ketals Tetrahedron Letters. 29: 4035-4038. DOI: 10.1016/S0040-4039(00)80410-4 |
0.789 |
|
| 1987 |
Mash EA. Homochiral ketals in organic synthesis. Enantioselective synthesis and absolute configuration of (-)-chokol A Journal of Organic Chemistry. 52: 4142-4143. DOI: 10.1021/Jo00227A044 |
0.378 |
|
| 1987 |
Mash EA, Nelson KA, Heidt PC. Diastereoselective cyclopropanation via homochiral ketals. Dioxolane structural effects Tetrahedron Letters. 28: 1865-1868. DOI: 10.1016/S0040-4039(00)95995-1 |
0.781 |
|
| 1987 |
Mash EA, Nelson KA. Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation of α,β-unsaturated ketals derived from 1,4-D1-O-benzyl-l-threitol Tetrahedron. 43: 679-692. DOI: 10.1016/S0040-4020(01)90002-X |
0.392 |
|
| 1987 |
Mash EA, Fryling JA. Homochiral ketals in organic synthesis. Enantioselective synthesis of (+)-β-eudesmol Journal of Organic Chemistry. 52: 3000-3003. |
0.793 |
|
| 1986 |
Nelson KA, Mash EA. Homochiral ketals in organic synthesis. Enantioselective synthesis of (R)-muscone Journal of Organic Chemistry. 51: 2721-2724. DOI: 10.1021/Jo00364A019 |
0.353 |
|
| 1986 |
Mash EA, Nelson KA. Homochiral ketals in organic synthesis. Enantioselective synthesis of [m.n.1] Propellanones Tetrahedron Letters. 27: 1441-1444. DOI: 10.1016/S0040-4039(00)84280-X |
0.381 |
|
| 1985 |
Mash EA, Nelson KA. Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation Journal of the American Chemical Society. 107: 8256-8258. DOI: 10.1002/Chin.198616105 |
0.352 |
|
| 1981 |
Mash EA, Gurria GM, Poulter CD. Farnesylpyrophosphate synthetase. Evidence for a rigid geranyl cation-pyrophosphate anion pair Journal of the American Chemical Society. 103: 3927-3929. DOI: 10.1002/Chin.198140066 |
0.471 |
|
| 1979 |
Poulter CD, Mash EA, Argyle JC, Muscio OJ, Rilling HC. Farnesyl pyrophosphate synthetase. Mechanistic studies of the 1′-4 coupling reaction in the terpene biosynthetic pathway [13] Journal of the American Chemical Society. 101: 6761-6763. DOI: 10.1021/Ja00516A053 |
0.488 |
|
| 1978 |
Poulter CD, Argyle JC, Mash EA. Farnesyl pyrophosphate synthetase. Mechanistic studies of the 1'-4 coupling reaction with 2-fluorogeranyl pyrophosphate. The Journal of Biological Chemistry. 253: 7227-33. PMID 701246 |
0.44 |
|
| 1977 |
Poulter CD, Argyle JC, Mash EA. Letter: Prenyltransferase. New evidence for an ionization-condensation-elimination mechanism with 2-fluorogeranyl pyrophosphate. Journal of the American Chemical Society. 99: 957-9. PMID 833388 DOI: 10.1021/Ja00445A056 |
0.46 |
|
| 1977 |
Poulter CD, Argyle JC, Mash EA. Formation of Fused, Spiro, and Metacyclophane Rings via Intramolecular Carbanion Attack on Arene- Chromium Complexes Journal of the American Chemical Society. 99: 959-961. DOI: 10.1021/Ja00445A057 |
0.511 |
|
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