Year |
Citation |
Score |
2019 |
Galler DJ, Bermudez GC, Parker KA. Multi-gram-scale synthesis of a versatile syn-anti stereotriad by a short and cost-effective route Arkivoc. 2019: 93-102. DOI: 10.24820/Ark.5550190.P010.902 |
0.747 |
|
2019 |
am Ende CW, Parker KA. Development of a 5-exo, 6-exo tandem radical cyclization to access bisabosqual A Tetrahedron. 75: 4255-4260. DOI: 10.1016/J.Tet.2019.05.001 |
0.334 |
|
2017 |
Elliott DC, Beutler JA, Parker KA. Importance of a 4-Alkyl Substituent for Activity in the Englerin Series. Acs Medicinal Chemistry Letters. 8: 746-750. PMID 28740610 DOI: 10.1021/Acsmedchemlett.7B00161 |
0.58 |
|
2016 |
Parker KA, Sampson NS. Precision Synthesis of Alternating Copolymers via Ring-Opening Polymerization of 1-Substituted Cyclobutenes. Accounts of Chemical Research. PMID 26914522 DOI: 10.1021/Acs.Accounts.5B00490 |
0.318 |
|
2015 |
Galler DJ, Parker KA. Five Easy Pieces. The Total Synthesis of Phosphoiodyn A (and Placotylene A). Organic Letters. PMID 26509219 DOI: 10.1021/Acs.Orglett.5B02642 |
0.774 |
|
2015 |
Tan L, Li G, Parker KA, Sampson NS. Ru-Catalyzed Isomerization Provides Access to Alternating Copolymers via Ring-Opening Metathesis Polymerization. Macromolecules. 48: 4793-4800. PMID 26243969 DOI: 10.1021/Acs.Macromol.5B01058 |
0.347 |
|
2015 |
Parker KA, Mindt TL. Regioselective 1,2-addition of organometallic reagents to unprotected juglones Tetrahedron Letters. 56: 3500-3502. DOI: 10.1016/J.Tetlet.2014.12.108 |
0.636 |
|
2014 |
Tan L, Parker KA, Sampson NS. A Bicyclo[4.2.0]octene-Derived Monomer Provides Completely Linear Alternating Copolymers via Alternating Ring-Opening Metathesis Polymerization (AROMP). Macromolecules. 47: 6572-6579. PMID 25328246 DOI: 10.1021/Ma5012039 |
0.344 |
|
2014 |
Parker KA, Lim HN. The mysterious case of the kingianins Strategies and Tactics in Organic Synthesis. 10: 51-78. DOI: 10.1016/B978-0-12-417185-5.00003-X |
0.349 |
|
2013 |
Piao D, Basavapathruni A, Iyidogan P, Dai G, Hinz W, Ray AS, Murakami E, Feng JY, You F, Dutschman GE, Austin DJ, Parker KA, Anderson KS. Bifunctional inhibition of HIV-1 reverse transcriptase: a first step in designing a bifunctional triphosphate. Bioorganic & Medicinal Chemistry Letters. 23: 1511-8. PMID 23380374 DOI: 10.1016/J.Bmcl.2012.12.015 |
0.587 |
|
2013 |
Piao D, Basavapathruni A, Iyidogan P, Dai G, Hinz W, Ray AS, Murakami E, Feng JY, You F, Dutschman GE, Austin DJ, Parker KA, Anderson KS. Bifunctional inhibition of HIV-1 reverse transcriptase: a first step in designing a bifunctional triphosphate. Bioorganic & Medicinal Chemistry Letters. 23: 1511-8. PMID 23380374 DOI: 10.1016/J.Bmcl.2012.12.015 |
0.587 |
|
2013 |
Lim HN, Parker KA. Total synthesis of kingianin A. Organic Letters. 15: 398-401. PMID 23273168 DOI: 10.1021/Ol303388K |
0.301 |
|
2013 |
Lim HN, Parker KA. Total synthesis of kingianin A. Organic Letters. 15: 398-401. PMID 23273168 DOI: 10.1021/Ol303388K |
0.301 |
|
2013 |
am Ende CW, Zhou Z, Parker KA. Total synthesis of (±)-bisabosqual A. Journal of the American Chemical Society. 135: 582-5. PMID 23268693 DOI: 10.1021/Ja3108577 |
0.505 |
|
2013 |
am Ende CW, Zhou Z, Parker KA. Total synthesis of (±)-bisabosqual A. Journal of the American Chemical Society. 135: 582-5. PMID 23268693 DOI: 10.1021/Ja3108577 |
0.505 |
|
2012 |
Lee J, Parker KA. A formal synthesis of (-)-englerin A by relay ring closing metathesis and transannular etherification. Organic Letters. 14: 2682-5. PMID 22564056 DOI: 10.1021/Ol3007524 |
0.668 |
|
2012 |
Lee J, Parker KA. A formal synthesis of (-)-englerin A by relay ring closing metathesis and transannular etherification. Organic Letters. 14: 2682-5. PMID 22564056 DOI: 10.1021/Ol3007524 |
0.668 |
|
2012 |
Tafrova JI, Pinkas-Sarafova A, Stolarzewicz E, Parker KA, Simon M. UVA/B exposure promotes the biosynthesis of dehydroretinol in cultured human keratinocytes. Molecular and Cellular Biochemistry. 364: 351-61. PMID 22307745 DOI: 10.1007/S11010-012-1237-7 |
0.724 |
|
2012 |
Tafrova JI, Pinkas-Sarafova A, Stolarzewicz E, Parker KA, Simon M. UVA/B exposure promotes the biosynthesis of dehydroretinol in cultured human keratinocytes. Molecular and Cellular Biochemistry. 364: 351-61. PMID 22307745 DOI: 10.1007/S11010-012-1237-7 |
0.724 |
|
2012 |
Kim K, Lauher JW, Parker KA. Asymmetric induction in 8Ï€ electrocyclizations. Design of a removable chiral auxiliary. Organic Letters. 14: 138-41. PMID 22146007 DOI: 10.1021/Ol202932X |
0.47 |
|
2012 |
Kim K, Lauher JW, Parker KA. Asymmetric induction in 8Ï€ electrocyclizations. Design of a removable chiral auxiliary. Organic Letters. 14: 138-41. PMID 22146007 DOI: 10.1021/Ol202932X |
0.47 |
|
2011 |
Parker KA, Mindt TL. Convergent Synthesis of 2H-Chromenes - a Formal [3+3] Cycloaddition by a One-pot, Three-Step Cascade. Tetrahedron. 67: 9779-9786. PMID 22259219 DOI: 10.1016/J.Tet.2011.09.068 |
0.635 |
|
2011 |
Parker KA, Mindt TL. Convergent Synthesis of 2H-Chromenes - a Formal [3+3] Cycloaddition by a One-pot, Three-Step Cascade. Tetrahedron. 67: 9779-9786. PMID 22259219 DOI: 10.1016/J.Tet.2011.09.068 |
0.635 |
|
2011 |
Parker KA, Denton RW. Iodoolefinic polypropionate building blocks from vinyl silanes with control of geometry by solvent and by neighboring group participation Tetrahedron Letters. 52: 2115-2116. DOI: 10.1016/J.Tetlet.2010.11.001 |
0.316 |
|
2009 |
Song A, Parker KA, Sampson NS. Synthesis of copolymers by alternating ROMP (AROMP). Journal of the American Chemical Society. 131: 3444-5. PMID 19275253 DOI: 10.1021/Ja809661K |
0.404 |
|
2008 |
Xie Q, Denton RW, Parker KA. A relay ring-closing metathesis synthesis of dihydrooxasilines, precursors of (Z)-iodo olefins. Organic Letters. 10: 5345-8. PMID 19006314 DOI: 10.1021/Ol802063H |
0.379 |
|
2008 |
Parker KA, Xie Q. Asymmetric catalysis route to anti,anti stereotriads, illustrated by applications. Organic Letters. 10: 1349-52. PMID 18314993 DOI: 10.1021/Ol702989G |
0.373 |
|
2008 |
Cao H, Parker KA. Short synthesis of the C1-C14 stretch of discodermolide from building blocks prepared by asymmetric catalysis. Organic Letters. 10: 1353-6. PMID 18311989 DOI: 10.1021/Ol7029933 |
0.556 |
|
2007 |
Parker KA, Wang P. Deconstruction-reconstruction strategy for accessing valuable polyketides. Preparation of the C15-C24 stereopentad of discodermolide. Organic Letters. 9: 4793-6. PMID 17924640 DOI: 10.1021/Ol702144U |
0.376 |
|
2006 |
Parker KA, Wang Z. Cleavable chiral auxiliaries in 8pi (8pi, 6pi) electrocyclizations. Organic Letters. 8: 3553-6. PMID 16869658 DOI: 10.1021/Ol061328L |
0.336 |
|
2006 |
Parker KA, Cao H. Scalable, catalytic asymmetric synthesis of syn, anti stereotriad building blocks for polypropionate antibiotics. Organic Letters. 8: 3541-4. PMID 16869655 DOI: 10.1021/Ol0612612 |
0.572 |
|
2006 |
Parker KA, Mindt TL, Koh YH. TESOTf-induced rearrangement of quinols. Efficient construction of the fully functionalized carbon skeleton of the griseusins by a divergent-reconvergent approach. Organic Letters. 8: 1759-62. PMID 16623544 DOI: 10.1021/Ol060206Q |
0.665 |
|
2006 |
Parker KA, Fokas D. Enantioselective synthesis of (-)-dihydrocodeinone: a short formal synthesis of (-)-morphine. The Journal of Organic Chemistry. 71: 449-55. PMID 16408951 DOI: 10.1021/Jo0513008 |
0.432 |
|
2006 |
Parker K, Cao H. Asymmetric Synthesis of syn-anti Stereotriad Building Blocks Synfacts. 2006: 1022-1022. DOI: 10.1055/S-2006-949287 |
0.538 |
|
2005 |
Parker KA, Chang W. Regioselectivity of rhodium nitrene insertion. Syntheses of protected glycals of l-daunosamine, d-saccharosamine, and l-ristosamine. Organic Letters. 7: 1785-8. PMID 15844906 DOI: 10.1021/Ol050356L |
0.541 |
|
2005 |
Parker KA, Su D. The “Reverse Polarity” Approach to Ravidomycin. Aryl C-Aminoglycosides from a Lithiated Aminoglycal. Cheminform. 36. DOI: 10.1081/Car-200059957 |
0.362 |
|
2005 |
Parker KA, Su DS. Models for the synthesis of pluramycin antibiotics. Rearrangement of mono-protected aminoglycal-substituted cyclohexadienediols Journal of Carbohydrate Chemistry. 24: 199-208. DOI: 10.1081/Car-200059936 |
0.397 |
|
2005 |
Parker KA, Lim Y-. Total Synthesis of (-)-SNF4435 C and (+)-SNF4435 D Synfacts. 2005: 8-8. DOI: 10.1055/S-2005-865345 |
0.326 |
|
2004 |
Parker KA, Lim YH. The total synthesis of (-)-SNF4435 C and (+)-SNF4435 D. Journal of the American Chemical Society. 126: 15968-9. PMID 15584723 DOI: 10.1021/Ja044733L |
0.357 |
|
2004 |
Parker KA, Katsoulis IA. A strategy for exploiting the pseudosymmetry of the C1-C13 stretch of discodermolide. Organic Letters. 6: 1413-6. PMID 15101755 DOI: 10.1021/Ol049735P |
0.741 |
|
2004 |
Parker KA, Lim YH. "Endo" and "exo" bicyclo[4.2.0]-octadiene isomers from the electrocyclization of fully substituted tetraene models for SNF 4435C and D. control of stereochemistry by choice of a functionalized substituent. Organic Letters. 6: 161-4. PMID 14723518 DOI: 10.1021/Ol036048+ |
0.363 |
|
2003 |
Parker KA, Chang W. A synthesis of L-vancosamine derivatives from non-carbohydrate precursors by a short sequence based on the Marshall, McDonald, and Du Bois reactions. Organic Letters. 5: 3891-3. PMID 14535736 DOI: 10.1021/Ol035479P |
0.602 |
|
2002 |
Parker KA, Mindt TL. Heterocycle annulation of enolizable vinyl quinone imides. Dihydroquinolines and quinolines from thermal 6pi-electrocyclizations and indoles from photochemical cyclizations. Organic Letters. 4: 4265-8. PMID 12443074 DOI: 10.1021/Ol026849X |
0.647 |
|
2002 |
Mural RJ, Adams MD, Myers EW, Smith HO, Miklos GL, Wides R, Halpern A, Li PW, Sutton GG, Nadeau J, Salzberg SL, Holt RA, Kodira CD, Lu F, Chen L, ... ... Parker KA, et al. A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome. Science (New York, N.Y.). 296: 1661-71. PMID 12040188 DOI: 10.1126/Science.1069193 |
0.492 |
|
2001 |
Parker KA, Mindt TL. Electrocyclic ring closure of the enols of vinyl quinones. A 2H-chromene synthesis. Organic Letters. 3: 3875-8. PMID 11720558 DOI: 10.1021/Ol0167199 |
0.662 |
|
2000 |
Parker KA, Georges AT. Reductive aromatization of quinols: synthesis of the C-arylglycoside nucleus of the papulacandins and chaetiacandin. Organic Letters. 2: 497-9. PMID 10814360 DOI: 10.1021/Ol991346L |
0.723 |
|
2000 |
Parker KA, Ding QJ. A general approach to angucyclines: Synthesis of hatomarubigin A, rubiginone B2, antibiotic X-1488E, 6-hydroxytetrangulol, and tetrangulol Tetrahedron. 56: 10249-10254. DOI: 10.1016/S0040-4020(00)00869-3 |
0.374 |
|
2000 |
Parker KA, Ding QJ. Relative reactivities of aminoglycosides and their synthetic equivalents in the C-glycosylation of aromatics. Synthesis of the pseudoaglycone (D-C-glycoside) of the benzanthrins Tetrahedron. 56: 10255-10261. DOI: 10.1016/S0040-4020(00)00868-1 |
0.372 |
|
1997 |
Parker KA, Dermatakis A. Enantioselective Synthesis of the Enyne A-Ring Synthon of the 1α-Hydroxy Vitamins D The Journal of Organic Chemistry. 62: 6692-6696. DOI: 10.1021/Jo970957T |
0.334 |
|
1996 |
Parker KA, Su DS. Synthesis of C-aryl furanosides by the 'reverse polarity' strategy Journal of Organic Chemistry. 61: 2191-2194. DOI: 10.1021/Jo951344O |
0.351 |
|
1995 |
Parker KA, Resnick L. The First Total Synthesis Of A Pyripyropene-Type Acat Inhibitor, ()-Geri-Bp001 Journal of Organic Chemistry. 60: 5726-5728. DOI: 10.1021/Jo00122A074 |
0.314 |
|
1995 |
Parker KA, Coburn CA, Koh Y. Reductive and Nonreductive Aromatization of Quinol Ketal Glycals. Models for the Preparation of C-Aryl Glycoside Natural Products The Journal of Organic Chemistry. 60: 2938-2941. DOI: 10.1021/Jo00114A057 |
0.336 |
|
1994 |
Parker KA. Novel methods for the synthesis of C-aryl glycoside natural products Pure and Applied Chemistry. 66: 2135-2138. DOI: 10.1351/Pac199466102135 |
0.398 |
|
1994 |
Parker KA, Fokas D. The radical cyclization approach to morphine. Models for highly oxygenated ring-III synthons Journal of Organic Chemistry. 59: 3933-3938. DOI: 10.1021/Jo00093A027 |
0.345 |
|
1994 |
Parker KA, Fokas D. Stereochemistry of radical cyclizations to side-chain olefinic bonds. An approach to control of the C-9 center of morphine Journal of Organic Chemistry. 59: 3927-3932. DOI: 10.1021/Jo00093A026 |
0.323 |
|
1994 |
Parker KA, Koh YH. Methodology for the regiospecific synthesis of bis C-aryl glycosides. Models for kidamycins Journal of the American Chemical Society. 116: 11149-11150. DOI: 10.1021/Ja00103A037 |
0.387 |
|
1992 |
Parker KA, Coburn CA, Johnson PD, Aristoff P. Reductive aromatization of quinols. New convenient methods for the regiospecific synthesis of p-hydroxy C-aryl glycals Journal of Organic Chemistry. 57: 5547-5550. DOI: 10.1021/Jo00046A049 |
0.366 |
|
1992 |
Parker KA, Kim HJ. A short stereospecific synthesis of (dl)-lycoramine. Control of relative stereochemistry by dipole effects The Journal of Organic Chemistry. 57: 752-755. DOI: 10.1021/Jo00028A066 |
0.342 |
|
1992 |
Parker KA, Coburn CA. Regioselectivity in intramolecular nucleophilic aromatic substitution. Synthesis of the potent anti HIV-I 8-halo TIBO analogs Journal of Organic Chemistry. 57: 97-100. DOI: 10.1021/Jo00027A019 |
0.353 |
|
1992 |
Parker KA, Fokas D. Convergent synthesis of (±)-dihydroisocodeine in 11 steps by the tandem radical cyclization strategy. A formal total synthesis of [±)-morphine Journal of the American Chemical Society. 114: 9688-9689. DOI: 10.1021/Ja00050A075 |
0.304 |
|
1991 |
Parker KA, Coburn CA. A four-step synthesis of TIBO R82150 Journal of Organic Chemistry. 56: 4600-4601. DOI: 10.1021/Jo00015A007 |
0.325 |
|
1991 |
Parker KA, Coburn CA. A strategy for the convergent synthesis of gilvocarcins via chromium carbene benzannulation. 1-O-Methyldefucogilvocarcin V in seven steps The Journal of Organic Chemistry. 56: 1666-1668. DOI: 10.1021/Jo00004A058 |
0.307 |
|
1991 |
Parker KA, Coburn CA. Reductive aromatization of quinol ketals: a new synthesis of C-aryl glycosides Journal of the American Chemical Society. 113: 8516-8518. DOI: 10.1021/Ja00022A046 |
0.398 |
|
1988 |
Parker KA, Meschwitz SM. Short stereoselective synthesis of L-nogalose. Carbohydrate Research. 172: 319-26. PMID 3370651 DOI: 10.1016/S0008-6215(00)90867-X |
0.312 |
|
1988 |
Parker KA, Casteel DA. Isoquinoline quinones. Preparation of saframycin intermediates and a total synthesis of mimosamycin The Journal of Organic Chemistry. 53: 2847-2850. DOI: 10.1021/Jo00247A038 |
0.437 |
|
1987 |
Parker KA, Spero DM, Koziski KA. Evaluation of some preparations of trialkoxyphthalic acid derivatives The Journal of Organic Chemistry. 52: 183-188. DOI: 10.1021/Jo00378A005 |
0.339 |
|
1986 |
Parker KA, Farmar JG. A stereocontrolled synthesis of dl-biflora-4,10(19),15-triene The Journal of Organic Chemistry. 51: 4023-4028. DOI: 10.1021/Jo00371A020 |
0.41 |
|
1986 |
Parker KA, Spero DM, Inman KC. Aryl radical-initiated cyclizations: Effect of aryl substituents on ring-size Tetrahedron Letters. 27: 2833-2836. DOI: 10.1016/S0040-4039(00)84654-7 |
0.337 |
|
1986 |
Parker KA, Breault GA. Strategies and intermediates for fredericamycin a synthesis: A 3-substituted 9-alkoxy cyclopenta(g)isoquinoline-1,8(2H)-dione Tetrahedron Letters. 27: 3835-3838. DOI: 10.1016/S0040-4039(00)83892-7 |
0.427 |
|
1985 |
Parker KA, Koziski KA, Breault G. Synthesis of 2,2-disubstituted 4,9-dihydroxy-1h-benz(f)indene-1,3(2h)diones. a model sequence for the synthesis of fredericamycin Tetrahedron Letters. 26: 2181-2182. DOI: 10.1016/S0040-4039(00)98956-1 |
0.309 |
|
1985 |
Parker KA, Farmar JG. Regioselectivity in the claisen rearrangement of bis-allylic alcohols: Electronic and steric effects of C-4 substituents Tetrahedron Letters. 26: 3655-3658. DOI: 10.1016/S0040-4039(00)89215-1 |
0.354 |
|
1984 |
Parker KA, Cohen ID, Padwa A, Dent W. Cycloadditions of non-stabilized azomethine ylides and quinones synthesis of the Reniera isoindole Tetrahedron Letters. 25: 4917-4920. DOI: 10.1016/S0040-4039(01)91258-4 |
0.395 |
|
1984 |
Parker KA, Cohen ID, Babine RE. Approaches to the isoquinoline quinone antibiotics. Additions of an amino acid derivative to a quinone monoacetal Tetrahedron Letters. 25: 3543-3546. DOI: 10.1016/S0040-4039(01)91071-8 |
0.426 |
|
1983 |
Parker KA, O'Fee R. Halonium-initiated cyclizations of allylic urethanes: stereo- and regioselectivity in functionalizing the olefinic bond Journal of the American Chemical Society. 105: 654-655. DOI: 10.1021/Ja00341A073 |
0.324 |
|
1982 |
Parker KA, Petraitis JJ, Kosley RW, Buchwald SL. Reactions of propargyl alcohols with amide acetals The Journal of Organic Chemistry. 47: 389-398. DOI: 10.1021/Jo00342A002 |
0.437 |
|
1982 |
Parker KA, Iqbal T. New approaches to the synthesis of vitamin D metabolites. 1. Stereocontrol in the intramolecular Diels-Alder reaction The Journal of Organic Chemistry. 47: 337-342. DOI: 10.1021/Jo00341A031 |
0.351 |
|
1982 |
Parker KA, Babine RE. Revision of the assignment of relative stereochemistry in sibirosamine: synthesis of methyl n-tosyl α-d-disirosaminopyranoside Tetrahedron Letters. 23: 1763-1766. DOI: 10.1016/S0040-4039(00)86735-0 |
0.314 |
|
1981 |
Parker KA, Sworin ME. Assignment of regiochemistry to substituted naphthoquinones by chemical and spectroscopic method; amino-, hydroxy-, and bromojuglone derivatives The Journal of Organic Chemistry. 46: 3218-3223. DOI: 10.1021/Jo00329A014 |
0.324 |
|
1981 |
Parker KA, Petraitis JJ. Synthesis of ansamycins: An approach to the naphthoquinone portion of the rifamycins and streptovaricins Tetrahedron Letters. 22: 397-400. DOI: 10.1016/0040-4039(81)80109-8 |
0.397 |
|
1980 |
Parker KA, Kallmerten J. Approaches to anthracyclines. 1. Conjugate aroylation of .alpha.,.beta.-unsaturated esters The Journal of Organic Chemistry. 45: 2614-2620. DOI: 10.1021/Jo01301A015 |
0.639 |
|
1980 |
Parker KA, Kang S. Regiospecific nucleophilic aromatic substitution: conjugate addition of active methylene compounds to quinone monoacetals and aromatization of the adducts Journal of Organic Chemistry. 45: 1218-1224. DOI: 10.1021/Jo01295A010 |
0.323 |
|
1980 |
Parker KA, Iqbal T. Approaches to anthracyclines: efficient syntheses of substituted naphthylacetonitriles The Journal of Organic Chemistry. 45: 1149-1151. DOI: 10.1021/Jo01294A045 |
0.341 |
|
1980 |
Parker KA, Kallmerten J. Efficient, regiospecific synthesis of anthracycline intermediates: total synthesis of daunomycin Journal of the American Chemical Society. 102: 5881-5886. DOI: 10.1002/Chin.198048313 |
0.719 |
|
1980 |
Parker KA, Kallmerten J. Approaches to anthracyclines. 2. Regiospecific annulative quinone synthesis The Journal of Organic Chemistry. 45: 2620-2625. DOI: 10.1002/Chin.198047186 |
0.702 |
|
1980 |
PARKER KA, KALLMERTEN J. ChemInform Abstract: APPROACHES TO ANTHRACYCLINES. 1. CONJUGATE AROYLATION OF α,β-UNSATURATED ESTERS Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198047134 |
0.653 |
|
1980 |
Parker KA, Kang S-. Regiospecific Nucleophilic Aromatic Substitution: Conjugate Addition Of Active Methylene Compounds To Quinone Monoacetals And Aromatization Of The Adducts Cheminform. 11. DOI: 10.1002/Chin.198029198 |
0.323 |
|
1979 |
Parker KA, Andrade JR. Studies on the synthesis of .alpha.-functionalized quinols: synthesis of jacaranone The Journal of Organic Chemistry. 44: 3964-3966. DOI: 10.1021/Jo01336A046 |
0.347 |
|
1979 |
Parker KA, Fedynyshyn TH. Synthesis of anhydrosibiromycinone: a new method for the direct synthesis of pyrrolo-1,4-benzodiazepin-5-ones Tetrahedron Letters. 20: 1657-1660. DOI: 10.1016/S0040-4039(01)93616-0 |
0.419 |
|
1979 |
Parker KA, Kallmerten JL. Regiospecific synthesis of linear quinone systems: efficient convergent synthesis of anthracycline intermediates Tetrahedron Letters. 20: 1197-1200. DOI: 10.1016/S0040-4039(01)86101-3 |
0.374 |
|
1978 |
Parker KA, Adamchuk MR. Intramolecular Diels-Alder reactions of the furan diene Tetrahedron Letters. 19: 1689-1692. DOI: 10.1016/S0040-4039(01)94641-6 |
0.332 |
|
1977 |
Parker KA, Petraitis JJ. A general synthesis of tertiary allenic amides: the reaction of propargyl alcohols with diethylformamide acetals Tetrahedron Letters. 18: 4561-4564. DOI: 10.1016/S0040-4039(01)83568-1 |
0.345 |
|
1977 |
PARKER KA, KOSLEY RWJ, BUCHWALD SL, PETRAITIS JJ. ChemInform Abstract: THE REACTION OF TERTIARY ETHYNYL ALCOHOLS WITH FORMAMIDE ACETALS- FORMATION OF DIENAMINES AND ENAMINE ORTHOFORMATES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197705164 |
0.371 |
|
1976 |
Parker KA, Kosley RW, Buchwald SL, Petraitis JJ. The reaction of tertiary ethynyl alcohols with formamide acetals: formation of dienamines and enamine orthoformates Journal of the American Chemical Society. 98: 7104-7105. DOI: 10.1021/Ja00438A074 |
0.441 |
|
1976 |
Parker KA, Kosley RW. The amide acetal condensation of propargyl alcohols: synthesis of γ-keto esters and silyl allenes under mild conditions Tetrahedron Letters. 17: 341-344. DOI: 10.1016/S0040-4039(00)93726-2 |
0.388 |
|
1975 |
Parker KA, Gibbons EG. A direct synthesis of primary amides from grignard reagents Tetrahedron Letters. 16: 981-984. DOI: 10.1016/S0040-4039(00)72622-0 |
0.398 |
|
1975 |
Parker KA, Kosley RW. Stereoselective synthesis of functionalized olefins: The orthoester claisen rearrangement of alkynyl allylic alcohols Tetrahedron Letters. 16: 691-694. DOI: 10.1016/S0040-4039(00)71957-5 |
0.335 |
|
1974 |
PARKER KA, JOHNSON WS. ChemInform Abstract: STUDY OF NOENZYMIC BIOGENETIC LIKE OLEFINIC CYCLIZATION, THE SYNTHESIS AND CYCLIZATION OF 4-(TRANS,TRANS-7,12-DIMETHYL-3,7,11-TRIDECATRIENYL)-3-METHYL-2-CYCLOHEXEN-1-OL AND ITS ALLYLIC ISOMER Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197426177 |
0.563 |
|
1973 |
Stork G, Gardner JO, Beckman RK, Parker KA. Haloketal cyclization. General method for the synthesis of functionalized cis bicyclic ketones Journal of the American Chemical Society. 95: 2014-2016. DOI: 10.1021/Ja00787A052 |
0.553 |
|
1973 |
STORK G, GARDNER JO, BOECKMAN RKJ, PARKER KA. ChemInform Abstract: CYCLISIERUNG VON HALOGENKETALEN, ALLGEMEINE METHODE ZUR SYNTH. VON FUNKTIONALISIERTEN CIS-BICYCLISCHEN KETONEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197322156 |
0.459 |
|
1971 |
Harding KE, Parker KA. Synthesis of 4-(alkenyl)-3-methyl-2-cyclohexen-1-ones Tetrahedron Letters. 12: 1633-1636. DOI: 10.1016/S0040-4039(01)87420-7 |
0.614 |
|
1969 |
Parker KA, Johnson WS. Synthesis of dendrolasin Tetrahedron Letters. 10: 1329-1332. DOI: 10.1016/S0040-4039(01)87877-1 |
0.504 |
|
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