Year |
Citation |
Score |
2010 |
KIESSLING AJ, MCCLURE CK. ChemInform Abstract: Conversion of Amides to Esters with Meerwein′s Reagent. Application to the Synthesis of a Carfentanil Precursor. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199726124 |
0.418 |
|
2010 |
MCCLURE CK, HANSEN KB. ChemInform Abstract: Diels-Alder Reactivity of a Ketovinylphosphonate with Cyclopentadiene and Furan. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199628212 |
0.369 |
|
2010 |
MCCLURE CK, JUNG K, GROTE CW, HANSEN K. ChemInform Abstract: Pentacovalent Phosphorus in Organic Synthesis: A New Route to Substituted Phosphonates Cheminform. 24: no-no. DOI: 10.1002/CHIN.199334211 |
0.313 |
|
2010 |
MCCLURE CK, GROTE CW, RHEINGOLD AL. ChemInform Abstract: Novel and Efficient Synthesis of Uracil Phosphonate Derivatives via Pentacovalent Oxaphospholenes. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199327234 |
0.337 |
|
2010 |
MCCLURE CK, JUNG K. ChemInform Abstract: Pentacovalent Oxaphosphorane Chemistry in Organic Synthesis: A New Route to Substituted Phosphonates. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199133226 |
0.326 |
|
2009 |
Jones TN, McClure CK. Synthesis of 4-ethoxy-2,3-dihydropyridinium tetrafluoroborate salts and 4-ethoxy-2,3-dihydropyridines Synlett. 1289-1290. DOI: 10.1055/s-0028-1088136 |
0.368 |
|
2009 |
Jones TN, McClure CK. ChemInform Abstract: Synthesis of 4-Ethoxy-2,3-dihydropyridinium Tetrafluoroborate Salts and 4-Ethoxy-2,3-dihydropyridines. Cheminform. 40. DOI: 10.1002/chin.200939141 |
0.39 |
|
2003 |
McClure CK, Link JS. 2-azabicyclo[2.2.2]octa-3,5-dione via a nitrile Diels-Alder reaction. The Journal of Organic Chemistry. 68: 8256-7. PMID 14535813 DOI: 10.1021/Jo034961I |
0.777 |
|
2003 |
McClure CK, Kiessling AJ, Link JS. Oxa-di-pi-methane photochemical rearrangement of quinuclidinones. Synthesis of pyrrolizidinones. Organic Letters. 5: 3811-3. PMID 14535716 DOI: 10.1021/Ol035202P |
0.698 |
|
2003 |
McClure CK, Kiessling AJ, Link JS. Oxa-di-π-methane Photochemical Rearrangement of Quinuclidinones. Synthesis of Pyrrolizidinones Organic Letters. 5: 3811-3813. DOI: 10.1021/ol035202p |
0.684 |
|
1999 |
Mcclure CK, Cai B, Spangler LH. Investigations of the Reaction of Pentacovalent Oxaphosphlenes with Isocyanates. Synthetic and Mechanistic Aspects Phosphorus, Sulfur, and Silicon and the Related Elements. 144: 709-712. DOI: 10.1080/10426509908546343 |
0.373 |
|
1999 |
Jung K, Lee M, McClure CK. Synthesis of Acyclic γ-Amino Mono-or Bisphosphonates Via Pentacovalent Oxaphosphorane Chemistry Phosphorus, Sulfur, and Silicon and the Related Elements. 147: 141-141. DOI: 10.1080/10426509908053551 |
0.317 |
|
1998 |
McClure CK, Kiessling AJ, Link JS. Formation of a carbon-nitrogen bond via a 5-exo-trig radical cyclization onto the nitrogen of an imidate ester Tetrahedron. 54: 7121-7126. DOI: 10.1016/S0040-4020(98)00351-2 |
0.674 |
|
1996 |
McClure C, Hansen K, Herzog K, Link J, Arnold F. Diels-Alder Reactivity of a Keto Vinylphosphonate. Empirical and Theoretical Observations. Application to the Syntheses of Phosphonate Analogues of Myo-Inositol Phosphorus, Sulfur, and Silicon and the Related Elements. 109: 333-336. DOI: 10.1080/10426509608046266 |
0.754 |
|
1996 |
McClure CK, Chenault HK. Chemoenzymatic Synthesis of an Enantiomerically Pure Lactone: A Three-Step Synthesis for Undergraduate Organic Chemistry Laboratory Journal of Chemical Education. 73: 467. DOI: 10.1021/ED073P467 |
0.338 |
|
1996 |
McClure CK, Herzog KJ, Bruch MD. Structure determination of the Diels-Alder product of a ketovinylphosphonate with E-1-acetoxy-1,3-butadiene Tetrahedron Letters. 37: 2153-2156. DOI: 10.1016/0040-4039(96)00236-5 |
0.316 |
|
1996 |
McClure CK, Hansen KB. Diels-Alder reactivity of a ketovinylphosphonate with cyclopentadiene and furan Tetrahedron Letters. 37: 2149-2152. DOI: 10.1016/0040-4039(96)00235-3 |
0.346 |
|
1991 |
McClure CK, Jung KY. Pentacovalent oxaphosphorane chemistry in organic synthesis: a new route to substituted phosphonates The Journal of Organic Chemistry. 56: 867-871. DOI: 10.1021/JO00002A072 |
0.308 |
|
1990 |
Paterson I, Goodman JM, Anne Lister M, Schumann RC, McClure CK, Norcross RD. Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: the use of enol diisopinocampheylborinates Tetrahedron. 46: 4663-4684. DOI: 10.1016/S0040-4020(01)85588-5 |
0.711 |
|
1990 |
PATERSON I, GOODMAN JM, LISTER MA, SCHUMANN RC, MCCLURE CK, NORCROSS RD. ChemInform Abstract: Enantio- and Diastereoselective Aldol Reactions of Achiral Ethyl and Methyl Ketones with Aldehydes: The Use of Enol Diisopinocampheylborinates. Cheminform. 21. DOI: 10.1002/CHIN.199044102 |
0.704 |
|
1989 |
Paterson I, McClure CK, Schumann RC. A short asymmetric synthesis of a C19–C27 segment of rifamycin S. Kinetic resolution in the aldol reactions of ethylketones using chiral boron reagents Tetrahedron Letters. 30: 1293-1296. DOI: 10.1016/S0040-4039(00)72740-7 |
0.584 |
|
1989 |
PATERSON I, MCCLURE CK, SCHUMANN RC. ChemInform Abstract: A Short Asymmetric Synthesis of a C19-C27 Segment (V) of Rifamycin S. Kinetic Resolution in the Aldol Reactions of Ethyl Ketones (.+-.)-(I) Using Chiral Boron Reagents. Cheminform. 20. DOI: 10.1002/CHIN.198938090 |
0.527 |
|
1987 |
Paterson I, McClure CK. Studies in macrolide synthesis: aldol condensations of chiral ethylketones via boron enolates Tetrahedron Letters. 28: 1229-1232. DOI: 10.1016/S0040-4039(00)95333-4 |
0.535 |
|
1987 |
PATERSON I, MCCLURE CK. ChemInform Abstract: Studies in Macrolide Synthesis: Aldol Condensations of Chiral Ethylketones via Boron Enolates. Cheminform. 18. DOI: 10.1002/CHIN.198735099 |
0.561 |
|
1987 |
PATERSON I, LISTER MA, MCCLURE CK. ChemInform Abstract: Enantioselective Aldol Condensations: The Use of Ketone Boron Enolates with Chiral Ligands Attached to Boron. Cheminform. 18. DOI: 10.1002/CHIN.198710132 |
0.486 |
|
1987 |
Vedejs E, Dent WH, Gapinski DM, McClure CK. Local conformer effects in unsaturated lactones Journal of the American Chemical Society. 109: 5437-5446. |
0.436 |
|
1986 |
Paterson I, Lister M, McClure CK. Enantioselective aldol condensations: The use of ketone boron enolates with chiral ligands attached to boron. Tetrahedron Letters. 27: 4787-4790. DOI: 10.1016/S0040-4039(00)85065-0 |
0.525 |
|
1986 |
VEDEJS E, EBERLEIN TH, MAZUR DJ, MCCLURE CK, PERRY DA, RUGGERI R, SCHWARTZ E, STULTS JS, VARIE DL, WILDE RG, WITTENBERGER S. ChemInform Abstract: Thioaldehyde Diels-Alder Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198649084 |
0.406 |
|
1986 |
VEDEJS E, MCCLURE CK. ChemInform Abstract: Hyperconjugative Effects of Allylic Substituents Are Not Important in Osmylations. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198626133 |
0.317 |
|
1986 |
Vedejs E, McClure CK. Hyperconjugative effects of allylic substituents are not important in osmylations Journal of the American Chemical Society. 108: 1094-1096. |
0.543 |
|
1986 |
Vedejs E, Eberlein TH, Mazur DJ, McClure CK, Perry DA, Ruggeri R, Schwartz E, Stults JS, Varie DL, Wilde RG, Wittenberger S. Thioaldehyde Diels-Alder reactions Journal of Organic Chemistry. 51: 1556-1562. |
0.745 |
|
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