Year |
Citation |
Score |
2020 |
Ali AIM, O'Donnell MJ, Scott WL, Samaritoni JG. A solid-phase synthetic route to N-acylated α-alkyl-d,l-homoserine lactones Tetrahedron Letters. 61: 152328. DOI: 10.1016/J.Tetlet.2020.152328 |
0.36 |
|
2019 |
O'Donnell MJ. Corrigendum to “Benzophenone Schiff bases of glycine derivatives: Versatile starting materials for the synthesis of amino acids and their derivatives” [Tetrahedron 75 (2019) 3667–3696] Tetrahedron. 75: 130460. DOI: 10.1016/J.Tet.2019.07.018 |
0.474 |
|
2019 |
O'Donnell MJ. Benzophenone Schiff bases of glycine derivatives: Versatile starting materials for the synthesis of amino acids and their derivatives Tetrahedron. 75: 3667-3696. DOI: 10.1016/J.Tet.2019.03.029 |
0.556 |
|
2016 |
Zhou Z, Scott WL, O'Donnell MJ. Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations. Molecules (Basel, Switzerland). 21. PMID 26999079 DOI: 10.3390/molecules21030350 |
0.334 |
|
2014 |
Samaritoni JG, Copes AT, Crews DK, Glos C, Thompson AL, Wilson C, O'Donnell MJ, Scott WL. Unexpected hydrolytic instability of N-acylated amino acid amides and peptides. The Journal of Organic Chemistry. 79: 3140-51. PMID 24617596 DOI: 10.1021/jo500273f |
0.347 |
|
2010 |
Scott WL, Zhou Z, Zajdel P, Paw?owski M, O'Donnell MJ. Solid-phase synthetic route to multiple derivatives of a fundamental peptide unit. Molecules (Basel, Switzerland). 15: 4961-83. PMID 20657403 DOI: 10.3390/molecules15074961 |
0.348 |
|
2010 |
O'Donnell MJ. ChemInform Abstract: The Preparation of Optically Active α-Amino Acids from the Benzophenone Imines of Glycine Derivatives Cheminform. 32: no-no. DOI: 10.1002/chin.200138280 |
0.379 |
|
2010 |
O'DONNELL MJ, DELGADO F, HOSTETTLER C, SCHWESINGER R. ChemInform Abstract: An Efficient Homogeneous Catalytic Enantioselective Synthesis of α-Amino Acid Derivatives. Cheminform. 30: no-no. DOI: 10.1002/chin.199908219 |
0.437 |
|
2010 |
O'DONNELL MJ, ESIKOVA IA, MI A, SHULLENBERGER DF, WU S. ChemInform Abstract: Amino Acid and Peptide Synthesis Using Phase-Transfer Catalysis Cheminform. 28: no-no. DOI: 10.1002/chin.199736299 |
0.345 |
|
2010 |
O'DONNELL MJ, LI M, BENNETT WD, GROTE T. ChemInform Abstract: Synthesis of β,γ-Unsaturated Amino Acid Derivatives by Alkyne Carbometalation-Palladium-Catalyzed Coupling with 2-Aza-π- allyl Palladium Complexes. Cheminform. 26: no-no. DOI: 10.1002/chin.199519201 |
0.374 |
|
2010 |
O'DONNELL MJ, WU S. ChemInform Abstract: A Catalytic Enantioselective Synthesis of α-Methyl Amino Acid Derivatives by Phase-Transfer Catalysis. Cheminform. 23: no-no. DOI: 10.1002/chin.199239274 |
0.424 |
|
2010 |
O'DONNELL MJ, COOK GK, RUSTERHOLZ DB. ChemInform Abstract: Oxygen Alkylation of Schiff Base Derivatives of Amino Acids. Cheminform. 23: no-no. DOI: 10.1002/chin.199219289 |
0.349 |
|
2010 |
O'DONNELL MJ, YANG X, LI M. ChemInform Abstract: 2-Aza-π-allylpalladium Complexes for the Synthesis of β- Carboxyaspartic Acid (ASA) Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199132233 |
0.323 |
|
2009 |
Scott WL, Zhou Z, Martynow JG, O'Donnell MJ. Solid-phase synthesis of amino- and carboxyl-functionalized unnatural alpha-amino acid amides. Organic Letters. 11: 3558-61. PMID 19624149 DOI: 10.1021/ol901279v |
0.336 |
|
2009 |
Green JE, Bender DM, Jackson S, O'Donnell MJ, McCarthy JR. ChemInform Abstract: Mitsunobu Approach to the Synthesis of Optically Active α,α-Disubstituted Amino Acids. Cheminform. 40. DOI: 10.1002/chin.200926061 |
0.336 |
|
2007 |
Scott WL, Martynow JG, Huffman JC, O'Donnell MJ. Solid-phase synthesis of multiple classes of peptidomimetics from versatile resin-bound aldehyde intermediates. Journal of the American Chemical Society. 129: 7077-88. PMID 17503818 DOI: 10.1021/Ja069188Y |
0.411 |
|
2007 |
Ramachandran PV, Madhi S, O'Donnell MJ. Synthesis of fluorinated glutamic acid derivatives via vinylalumination Journal of Fluorine Chemistry. 128: 78-83. DOI: 10.1016/j.jfluchem.2006.10.003 |
0.385 |
|
2006 |
Ruiz-Sanchez E, O'Donnell MJ. Characterization of salicylate uptake across the basolateral membrane of the malpighian tubules of Drosophila melanogaster. Journal of Insect Physiology. 52: 920-8. PMID 16934829 DOI: 10.1016/j.jinsphys.2006.05.013 |
0.326 |
|
2006 |
O'Donnell MJ, Keeton JD, Van Khau V, Bollinger JC. The regioselective α-alkylation of the benzophenone imine of glycinamide, alaninamide, and related derivatives Canadian Journal of Chemistry. 84: 1301-1312. DOI: 10.1139/V06-088 |
0.318 |
|
2005 |
Ramachandran PV, Madhi S, Bland-Berry L, Ram Reddy MV, O'Donnell MJ. Catalytic enantioselective synthesis of glutamic acid derivatives via tandem conjugate addition-elimination of activated allylic acetates under chiral PTC conditions. Journal of the American Chemical Society. 127: 13450-1. PMID 16190680 DOI: 10.1021/Ja052638M |
0.484 |
|
2005 |
Alsina J, Scott WL, O'Donnell MJ. Solid-phase synthesis of α-substituted proline hydantoins and analogs Tetrahedron Letters. 46: 3131-3135. DOI: 10.1016/j.tetlet.2005.01.163 |
0.367 |
|
2004 |
O'Donnell MJ. The enantioselective synthesis of alpha-amino acids by phase-transfer catalysis with achiral Schiff base esters. Accounts of Chemical Research. 37: 506-17. PMID 15311949 DOI: 10.1021/Ar0300625 |
0.474 |
|
2004 |
Scott WL, Alsina J, Kennedy JH, O'Donnell MJ. Solid-phase synthesis of constrained terminal and internal lactam peptidomimetics. Organic Letters. 6: 1629-32. PMID 15128253 DOI: 10.1021/Ol049547Z |
0.435 |
|
2004 |
O'Donnell MJ, Scott WL. Unnatural Amino Acid and Peptide Synthesis (UPS) Cheminform. 35. DOI: 10.1002/CHIN.200416268 |
0.325 |
|
2003 |
O'Donnell MJ, Cooper JT, Mader MM. Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of beta-substituted alpha-amino acid derivatives. Journal of the American Chemical Society. 125: 2370-1. PMID 12603106 DOI: 10.1021/Ja0298794 |
0.674 |
|
2003 |
Scott WL, Alsina J, O'Donnell MJ. The manual and automated solid-phase synthesis of α-substituted prolines and homologues Journal of Combinatorial Chemistry. 5: 684-692. DOI: 10.1021/Cc030037Q |
0.509 |
|
2003 |
O'Donnell MJ, Alsina J, Scott WL. Solid-phase synthesis and utilization of side-chain reactive unnatural amino acids Tetrahedron Letters. 44: 8403-8406. DOI: 10.1016/J.Tetlet.2003.09.119 |
0.503 |
|
2002 |
O'Donnell MJ, Drew MD, Cooper JT, Delgado F, Zhou C. The enantioselective synthesis of alpha-amino acid derivatives via organoboranes. Journal of the American Chemical Society. 124: 9348-9. PMID 12167010 DOI: 10.1021/Ja017522E |
0.672 |
|
2002 |
Scott WL, O'Donnell MJ, Delgado F, Alsina J. A solid-phase synthetic route to unnatural amino acids with diverse side-chain substitutions. The Journal of Organic Chemistry. 67: 2960-9. PMID 11975553 DOI: 10.1021/Jo016236I |
0.487 |
|
2001 |
O'Donnell MJ, Delgado F, Domı́nguez E, de Blas J, Scott WL. Enantioselective solution- and solid-phase synthesis of glutamic acid derivatives via Michael addition reactions Tetrahedron: Asymmetry. 12: 821-828. DOI: 10.1016/S0957-4166(01)00116-1 |
0.463 |
|
2001 |
Scott WL, Delgado F, Lobb K, Pottorf RS, O'Donnell MJ. Solid-phase synthesis of amino amides and peptide amides with unnatural side chains Tetrahedron Letters. 42: 2073-2076. DOI: 10.1016/S0040-4039(01)00090-9 |
0.435 |
|
2001 |
O'Donnell MJ, Delgado F. Enantiomeric enrichment of α-amino acid derivatives: recrystallization of N-Fmoc α-amino acid tert-butyl esters Tetrahedron. 57: 6641-6650. DOI: 10.1016/S0040-4020(01)00554-3 |
0.521 |
|
2000 |
O'Donnell MJ, Drew MD, Pottorf RS, Scott WL. UPS on Weinreb resin: a facile solid-phase route to aldehyde and ketone derivatives of "unnatural" amino acids and peptides. Journal of Combinatorial Chemistry. 2: 172-81. PMID 10757096 DOI: 10.1021/cc990071y |
0.349 |
|
1999 |
O'Donnell MJ, Delgado F, Drew MD, Pottorf RS, Zhou C, Scott WL. Solid-phase synthesis of unnatural α-amino acid derivatives using a resin-bound glycine cation equivalent Tetrahedron Letters. 40: 5831-5835. DOI: 10.1016/S0040-4039(99)01101-6 |
0.532 |
|
1999 |
O'Donnell MJ, Delgado F, Pottorf RS. Enantioselective solid-phase synthesis of α-amino acid derivatives Tetrahedron. 55: 6347-6362. DOI: 10.1016/S0040-4020(99)00211-2 |
0.538 |
|
1998 |
O'Donnell MJ, Delgado F, Hostettler C, Schwesinger R. An efficient homogeneous catalytic enantioselective synthesis of α-amino acid derivatives Tetrahedron Letters. 39: 8775-8778. DOI: 10.1016/S0040-4039(98)01995-9 |
0.508 |
|
1998 |
Domínguez E, O'Donnell MJ, Scott WL. Solid-phase synthesis of substituted glutamic acid derivatives via Michael addition reactions Tetrahedron Letters. 39: 2167-2170. DOI: 10.1016/S0040-4039(98)00165-8 |
0.515 |
|
1997 |
O'Donnell MJ, Chen N, Zhou C, Murray A, Kubiak CP, Yang F, Stanley GG. Efficient Catalytic Enantioselective Reaction of a Glycine Cation Equivalent with Malonate AnionsviaPalladium Catalysis The Journal of Organic Chemistry. 62: 3962-3975. DOI: 10.1021/Jo961869W |
0.422 |
|
1997 |
Griffith DL, O'Donnell MJ, Pottorf RS, Scott WL, Porco JA. Tandem UPS: Sequential mono- and dialkylation of resin-bound glycine via automated synthesis Tetrahedron Letters. 38: 8821-8824. DOI: 10.1016/S0040-4039(97)10484-1 |
0.526 |
|
1997 |
O'Donnell MJ, Lugar CW, Pottorf RS, Zhou C, Scott WL, Cwi CL. Solid-phase synthesis of unnatural amino acids using unactivated alkyl halides Tetrahedron Letters. 38: 7163-7166. DOI: 10.1016/S0040-4039(97)01762-0 |
0.485 |
|
1997 |
Scott WL, Zhou C, Fang Z, O'Donnell MJ. The solid phase synthesis of α,α-disubstituted unnatural amino acids and peptides (di-UPS) Tetrahedron Letters. 38: 3695-3698. DOI: 10.1016/S0040-4039(97)00715-6 |
0.486 |
|
1996 |
O'Donnell MJ, Zhou C, Chen N. Preparation of optically active β-carboxyaspartic acid derivatives via Pd(0)-catalyzed asymmetric substitution of Schiff base acetates Tetrahedron-Asymmetry. 7: 621-624. DOI: 10.1016/0957-4166(96)00048-1 |
0.428 |
|
1995 |
O'Donnell MJ, Zhou C, Mi A, Chen N, Kyle JA, Andersson PG. Palladium-catalyzed reaction of a malonate anion with a glycine cation equivalent: Bis-phosphine ligands and in situ catalyst formation Tetrahedron Letters. 36: 4205-4208. DOI: 10.1016/0040-4039(95)00795-E |
0.328 |
|
1994 |
O'Donnell MJ, Li M, Bennett WD, Grote T. Synthesis of β,γ-unsaturated amino acid derivatives by alkyne carbometalation-palladium catalyzed coupling with 2-aza-π-allyl palladium complexes Tetrahedron Letters. 35: 9383-9386. DOI: 10.1016/S0040-4039(00)78548-0 |
0.478 |
|
1994 |
O'Donnell MJ, Lawley LK, Pushpavanam PB, Burger A, Bordwell FG, Zhang XM. Preparation of an α-aminophosphonate cation equivalent and its reaction with organoboranes Tetrahedron Letters. 35: 6421-6424. DOI: 10.1016/S0040-4039(00)78235-9 |
0.407 |
|
1994 |
O'Donnell MJ, Wu S, Huffman JC. A new active catalyst species for enantioselective alkylation by phase-transfer catalysis Tetrahedron. 50: 4507-4518. DOI: 10.1016/S0040-4020(01)89382-0 |
0.382 |
|
1992 |
O'Donnell MJ, Wu S. A catalytic enantioselective synthesis of α-methyl amino acid derivatives by phase-transfer catalysis Tetrahedron: Asymmetry. 3: 591-594. DOI: 10.1016/S0957-4166(00)82288-0 |
0.522 |
|
1991 |
O'Donnell MJ, Cook GK, Rusterholz DB. Oxygen Alkylation of Schiff Base Derivatives of Amino Acids Synthesis. 1991: 989-993. DOI: 10.1055/S-1991-26625 |
0.429 |
|
1990 |
O'Donnell MJ, Yang X, Li M. 2-aza-π-allylpalladium complexes for the synthesis of β-carboxyaspartic acid (asa) derivatives Tetrahedron Letters. 31: 5135-5138. DOI: 10.1016/S0040-4039(00)97824-9 |
0.473 |
|
1990 |
O'Donnell MJ, Arasappan A, Hornback WJ, Huffman JC. Preparation and Wittig reactions of an α-keto amino acid derivative Tetrahedron Letters. 31: 157-160. DOI: 10.1016/S0040-4039(00)94358-2 |
0.451 |
|
1990 |
O'DONNELL MJ, ARASAPPAN A, HORNBACK WJ, HUFFMAN JC. ChemInform Abstract: Preparation and Wittig Reactions of an α-Keto Amino Acid Derivative. Cheminform. 21. DOI: 10.1002/chin.199035111 |
0.441 |
|
1990 |
O'DONNELL MJ, BENNETT WD, JACOBSEN WN, MA Y. ChemInform Abstract: Phenylation of Amino Acid Derivatives (I), (IV): A New Route to α-Phenyl-α-Substituted Amino Acids (III), (V). Cheminform. 21. DOI: 10.1002/chin.199009321 |
0.398 |
|
1989 |
O'donnell MJ, Rusterholz DB. Synthetic of α-Methylhistidine by Catalytic Phase-Transfer Alkylations Synthetic Communications. 19: 1157-1165. DOI: 10.1080/00397918908054518 |
0.411 |
|
1989 |
O'Donnell MJ, Bennett WD, Wu S. The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis Journal of the American Chemical Society. 111: 2353-2355. DOI: 10.1021/Ja00188A089 |
0.465 |
|
1989 |
O'Donnell MJ, Bennett WD, Jacobsen WN, Ma Y. Phenylation of amino acid derivatives: A new route to α-phenyl-α-substituted amino acids Tetrahedron Letters. 30: 3913-3914. DOI: 10.1016/S0040-4039(00)99282-7 |
0.498 |
|
1989 |
O'DONNELL MJ, BENNETT WD, WU S. ChemInform Abstract: The Stereoselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis. Cheminform. 20. DOI: 10.1002/chin.198926289 |
0.411 |
|
1989 |
O'DONNELL MJ, BENNETT WD, BRUDER WA, JACOBSEN WN, KNUTH K, LECLEF B, POLT RL, BORDWELL FG, MROZACK SR, CRIPE TA. ChemInform Abstract: Acidities of Glycine Schiff Bases and Alkylation of Their Conjugate Bases. Cheminform. 20. DOI: 10.1002/chin.198912054 |
0.372 |
|
1989 |
O'DONNELL MJ, BENNETT WD. ChemInform Abstract: Synthesis of Amino Acids by Reaction of an Electrophilic Glycine Cation Equivalent with Neutral Carbon Nucleophiles. Cheminform. 20. DOI: 10.1002/chin.198901132 |
0.4 |
|
1988 |
O'Donnell MJ, Bennett WD, Bruder WA, Jacobsen WN, Knuth K, LeClef B, Polt RL, Bordwell FG, Mrozack SR, Cripe TA. Acidities of glycine Schiff bases and alkylation of their conjugate bases Journal of the American Chemical Society. 110: 8520-8525. DOI: 10.1021/ja00233a031 |
0.358 |
|
1988 |
O'Donnell MJ, Bennett WD, Bruder WA, Jacobsen WN, Knuth K, LeClef B, Polt RL, Bordwell FG, Mrozack SR, Cripe TA. Acidities of glycine Schiff bases and alkylation of their conjugate bases Journal of the American Chemical Society. 110: 8520-8525. DOI: 10.1021/Ja00233A031 |
0.367 |
|
1988 |
O'Donnell MJ, Bennett WD. The synthesis of amino acids by reaction of an electrophilic glycine cation equivalent with neutral carbon nucleophiles Tetrahedron. 44: 5389-5401. DOI: 10.1016/S0040-4020(01)86045-2 |
0.395 |
|
1987 |
McCarthy JR, Barney CL, O'Donnell MJ, Huffman JC. New pathway for the reaction of difluorocarbene with imines Journal of the Chemical Society, Chemical Communications. 469-470. DOI: 10.1039/C39870000469 |
0.313 |
|
1985 |
O'Donnell MJ, Falmagne J. The synthesis of amino acids via organoboranes Journal of the Chemical Society, Chemical Communications. 1168-1169. DOI: 10.1039/C39850001168 |
0.513 |
|
1985 |
O'Donnell MJ, Barney CL, McCarthy JR. A convenient synthesis of erythro- and threo-3-fluorophenyl- alanine from a protected glycine synthon Tetrahedron Letters. 26: 3067-3070. DOI: 10.1016/S0040-4039(00)98620-9 |
0.306 |
|
1985 |
O'Donnell MJ, Bennett WD, Polt RL. Preparation of an electrophilic glycine cation equivalent and its reaction with heteroatom nucleophiles Tetrahedron Letters. 26: 695-698. DOI: 10.1016/S0040-4039(00)89111-X |
0.467 |
|
1985 |
O'Donnell MJ, Falmagne JB. The synthesis of amino acids by reaction of an electrophilic glycine cation equivalent with carbon nucleophiles Tetrahedron Letters. 26: 699-702. DOI: 10.1016/S0040-4020(01)86045-2 |
0.517 |
|
1985 |
O'DONNELL MJ, FALMAGNE J. ChemInform Abstract: THE SYNTHESIS OF AMINO ACIDS VIA ORGANOBORANES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198551142 |
0.501 |
|
1985 |
O'DONNELL MJ, BENNETT WD, POLT RL, FALMAGNE J. ChemInform Abstract: Preparation of an Electrophilic Glycine Cation Equivalent and Its Reaction with Heteroatom Nucleophiles. The Synthesis of Amino Acids by Reaction of an Electrophilic Glycine Cation Equivalent with Carbon Nucleophiles. Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198525356 |
0.475 |
|
1985 |
O'DONNELL MJ, BRUDER WA, DAUGHERTY BW, LIU D, WOJCIECHOWSKI K. ChemInform Abstract: NITROGEN ALKYLATION OF SCHIFF BASES AND AMIDINES AS A ROUTE TO N-ALKYL AMINO ACIDS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198501157 |
0.373 |
|
1984 |
O'Donnell MJ, Wojciechowski K, Ghosez L, Navarro M, Sainte F, Antoine J. Alkylation of Protected α-Amino Acid Derivatives in the Presence of Potassium Carbonate Synthesis. 1984: 313-315. DOI: 10.1055/S-1984-30822 |
0.47 |
|
1984 |
O'Donnell MJ, Bruder WA, Eckrich TM, Shullenberger DF, Staten GS. Simple Syntheses of the Amino Acids: 1-Aminocyclopropane-1-carboxylic Acid, Cycloleucine and 2,6-Diaminopimelic Acid Synthesis. 1984: 127-128. DOI: 10.1055/S-1984-30749 |
0.401 |
|
1984 |
O'Donnell MJ, Bruder WA, Daugherty BW, Liu D, Wojciechowski K. Nitrogen Alkylation of schiff bases and amidines as a route to N-alkyl amino acids Tetrahedron Letters. 25: 3651-3654. DOI: 10.1016/0040-4039(84)80096-9 |
0.481 |
|
1984 |
O'DONNELL MJ, WOJCIECHOWSKI K, GHOSEZ L, NAVARRO M, SAINTE F, ANTOINE J. ChemInform Abstract: ALKYLATION OF PROTECTED α-AMINO ACID DERIVATIVES IN THE PRESENCE OF POTASSIUM CARBONATE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198436148 |
0.381 |
|
1984 |
O'DONNELL MJ, BRUDER WA, ECKRICH TM, SHULLENBERGER DF, STATEN GS. ChemInform Abstract: SIMPLE SYNTHESES OF THE AMINO ACIDS: 1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID, CYCLOLEUCINE AND 2,6-DIAMINOPIMELIC ACID Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198426325 |
0.384 |
|
1983 |
O'DONNELL MJ, LECLEF B, RUSTERHOLZ D, GHOSEZ L, ANTOINE J, NAVARRO M. ChemInform Abstract: α-METHYL AMINO ACIDS BY CATALYTIC PHASE-TRANSFER ALKYLATIONS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198308157 |
0.383 |
|
1983 |
GHOSEZ L, ANTOINE J, DEFFENSE E, NAVARRO M, LIBERT V, O'DONNELL MJ, BRUDER WA, WILLEY K, WOJCIECHOWSKI K. ChemInform Abstract: SYNTHESIS OF AMINO ACIDS. ALKYLATION OF ALDIMINE AND KETIMINE DERIVATIVES OF GLYCINE ETHYL ESTER UNDER VARIOUS PHASE-TRANSFER CONDITIONS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198308156 |
0.425 |
|
1982 |
O'Donnell MJ, Polt RL. A mild and efficient route to Schiff base derivatives of amino acids The Journal of Organic Chemistry. 47: 2663-2666. DOI: 10.1021/jo00134a030 |
0.39 |
|
1982 |
O'Donnell MJ, LeClef B, Rusterholz DB, Ghosez L, Antoine JP, Navarro M. α-methyl amino acids by catalytic phase-transfer alkylations Tetrahedron Letters. 23: 4259-4262. DOI: 10.1016/S0040-4039(00)88719-5 |
0.45 |
|
1982 |
Ghosez L, Antoine JP, Deffense E, Navarro M, Libert V, O'Donnell MJ, Bruder WA, Willey K, Wojciechowski K. Synthesis of amino acids. Alkylation of aldimine and ketimine derivatives of glycine ethyl ester under various phase-transfer conditions Tetrahedron Letters. 23: 4255-4258. DOI: 10.1016/S0040-4039(00)88718-3 |
0.404 |
|
1982 |
O'DONNELL MJ, POLT RL. ChemInform Abstract: A MILD AND EFFICIENT ROUTE TO SCHIFF BASE DERIVATIVES OF AMINO ACIDS Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198251347 |
0.402 |
|
1982 |
O'Donnell MJ, Polt RL. A mild and efficient route to Schiff base derivatives of amino acids Journal of Organic Chemistry. 47: 2663-2666. DOI: 10.1002/Chin.198251347 |
0.48 |
|
1980 |
WIBERG KB, O'DONNELL MJ. ChemInform Abstract: PREPARATION AND DIELS-ALDER REACTIONS OF THE (N)(1,4)NAPHTHALENOPHANES. ISOLATION OF A PADDLANE DERIVATIVE CONTAINING THE TRICYCLO(14.2.2.21,6)DOCOSANE RING SYSTEM Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198005213 |
0.342 |
|
1979 |
Wiberg KB, O'Donnell MJ. Preparation and Diels-Alder reactions of the [n](1,4)naphthalenophanes. Isolation of a paddlane derivative containing the tricyclo[14.2.2.21,6]docosane ring system Journal of the American Chemical Society. 101: 6660-6666. DOI: 10.1021/Ja00516A029 |
0.332 |
|
1979 |
O'DONNELL MJ, ECKRICH TM. ChemInform Abstract: THE SYNTHESIS OF AMINO ACID DERIVATIVES BY CATALYTIC PHASE-TRANSFER ALKYLATIONS Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197917358 |
0.424 |
|
1978 |
O'Donnell MJ, Boniece JM, Earp SE. The synthesis of amino acids by phase-transfer reactions Tetrahedron Letters. 19: 2641-2644. DOI: 10.1016/S0040-4039(01)91563-1 |
0.484 |
|
1978 |
O'Donnell MJ, Eckrich TM. The synthesis of amino acid derivatives by catalytic phase-transfer alkylations Tetrahedron Letters. 19: 4625-4628. DOI: 10.1016/S0040-4039(01)85688-4 |
0.52 |
|
1978 |
O'DONNELL MJ, BONIECE JM, EARP SE. ChemInform Abstract: THE SYNTHESIS OF AMINO ACIDS BY PHASE-TRANSFER REACTIONS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197846174 |
0.404 |
|
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