| Year |
Citation |
Score |
| 2021 |
MaBouDi H, Barron AB, Li S, Honkanen M, Loukola OJ, Peng F, Li W, Marshall JAR, Cope A, Vasilaki E, Solvi C. Non-numerical strategies used by bees to solve numerical cognition tasks. Proceedings. Biological Sciences. 288: 20202711. PMID 33593192 DOI: 10.1098/rspb.2020.2711 |
0.4 |
|
| 2020 |
MaBouDi H, Marshall JAR, Barron AB. Honeybees solve a multi-comparison ranking task by probability matching. Proceedings. Biological Sciences. 287: 20201525. PMID 32873200 DOI: 10.1098/rspb.2020.1525 |
0.4 |
|
| 2018 |
Cope AJ, Vasilaki E, Minors D, Sabo C, Marshall JAR, Barron AB. Abstract concept learning in a simple neural network inspired by the insect brain. Plos Computational Biology. 14: e1006435. PMID 30222735 DOI: 10.1371/journal.pcbi.1006435 |
0.4 |
|
| 2017 |
Cope AJ, Sabo C, Vasilaki E, Barron AB, Marshall JA. A computational model of the integration of landmarks and motion in the insect central complex. Plos One. 12: e0172325. PMID 28241061 DOI: 10.1371/journal.pone.0172325 |
0.4 |
|
| 2015 |
Barron AB, Gurney KN, Meah LF, Vasilaki E, Marshall JA. Decision-making and action selection in insects: inspiration from vertebrate-based theories. Frontiers in Behavioral Neuroscience. 9: 216. PMID 26347627 DOI: 10.3389/fnbeh.2015.00216 |
0.4 |
|
| 2013 |
Bruggink LD, Marshall JA. Altered patterns of norovirus GII.b recombinant forms in gastroenteritis outbreaks in Victoria, Australia, 2002-2005 compared to 2006-2011. Journal of Medical Virology. 85: 1433-43. PMID 23765780 DOI: 10.1002/jmv.23633 |
0.01 |
|
| 2012 |
Bruggink LD, Oluwatoyin O, Sameer R, Witlox KJ, Marshall JA. Molecular and epidemiological features of gastroenteritis outbreaks involving genogroup I norovirus in Victoria, Australia, 2002-2010. Journal of Medical Virology. 84: 1437-48. PMID 22825823 DOI: 10.1002/jmv.23342 |
0.01 |
|
| 2010 |
Marshall JA, Griot CA, Chobanian HR, Myers WH. Synthesis of a lactone diastereomer of the cembranolide uprolide D. Organic Letters. 12: 4328-31. PMID 20795632 DOI: 10.1021/ol101776e |
1 |
|
| 2008 |
Marshall JA, Hann RK. A cascade cyclization route to adjacent bistetrahydrofurans from chiral triepoxyfarnesyl bromides. The Journal of Organic Chemistry. 73: 6753-7. PMID 18683983 DOI: 10.1021/jo801188w |
1 |
|
| 2008 |
Marshall JA, Eidam PM. A formal synthesis of the callipeltoside aglycone. Organic Letters. 10: 93-6. PMID 18052287 DOI: 10.1021/ol702024b |
1 |
|
| 2008 |
Marshall JA. Preparation and Addition Reactions of Allylic and Allenic Tin and Indium Reagents Lewis Acids in Organic Synthesis. 453-522. DOI: 10.1002/9783527618309.ch10 |
1 |
|
| 2007 |
Marshall JA. Chiral allylic and allenic metal reagents for organic synthesis. The Journal of Organic Chemistry. 72: 8153-66. PMID 17595141 DOI: 10.1021/jo070787c |
1 |
|
| 2007 |
Marshall JA, Sabatini JJ, Valeriote F. ABC synthesis and antitumor activity of a series of Annonaceous acetogenin analogs with a threo, trans, threo, trans, threo-bis-tetrahydrofuran core unit. Bioorganic & Medicinal Chemistry Letters. 17: 2434-7. PMID 17329102 DOI: 10.1016/j.bmcl.2007.02.033 |
1 |
|
| 2007 |
Marshall JA, Eidam P, Eidam HS. Synthesis of 4-triisopropylsilyl-3-butyn-2-ol by asymmetric transfer hydrogenation Organic Syntheses. 84: 120-128. |
1 |
|
| 2006 |
Marshall JA, Herold M, Eidam HS, Eidam P. Palladium- and copper-catalyzed 1,4-additions of organozinc compounds to conjugated aldehydes. Organic Letters. 8: 5505-8. PMID 17107058 DOI: 10.1021/ol062154a |
1 |
|
| 2006 |
Marshall JA, Mikowski AM. Synthesis of a bistetrahydrofuran C17-C32 fragment of the polyether antibiotic ionomycin. Organic Letters. 8: 4375-8. PMID 16956230 DOI: 10.1021/ol061826u |
1 |
|
| 2006 |
Marshall JA, Sabatini JJ. An outside-in approach to adjacent bistetrahydrofuran annonaceous acetogenins with C2 core symmetry. Total synthesis of asimicin and a C32 analogue. Organic Letters. 8: 3557-60. PMID 16869659 DOI: 10.1021/ol061352z |
1 |
|
| 2006 |
Marshall JA, Eidam P, Eidam HS. (R)- and (S)-4-TIPS-3-butyn-2-ol. Useful precursors of chiral allenylzinc and indium reagents. The Journal of Organic Chemistry. 71: 4840-4. PMID 16776511 DOI: 10.1021/jo060542k |
1 |
|
| 2006 |
Marshall JA, Mikowski AM, Bourbeau MP, Schaaf GM, Valeriote F. Leptostatin: a synthetic hybrid of the cytotoxic polyketides callystatin A and leptomycin B. Bioorganic & Medicinal Chemistry Letters. 16: 320-3. PMID 16271470 DOI: 10.1016/j.bmcl.2005.09.084 |
1 |
|
| 2005 |
Marshall JA, Schaaf G, Nolting A. Synthesis of the C6-C21 segment of amphidinolide E. Organic Letters. 7: 5331-3. PMID 16268571 DOI: 10.1021/ol0523493 |
1 |
|
| 2005 |
Marshall JA, Sabatini JJ. Synthesis of cis- and trans-2,5-disubstituted tetrahydrofurans by a tandem dihydroxylation-SN2 cyclization sequence. Organic Letters. 7: 4819-22. PMID 16235897 DOI: 10.1021/ol051507n |
1 |
|
| 2005 |
Marshall JA, Mulhearn JJ. Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal. Organic Letters. 7: 1593-6. PMID 15816760 DOI: 10.1021/ol050289v |
1 |
|
| 2005 |
Marshall JA, Chobanian H. Lipase-catalyzed resolution of 4-trimethylsilyl-3-butyn-2-ol and conversion of the (R)-enantiomer to (R)-3-butyn-2-yl mesylate and (P)-1-tributylstannyl-1, 2-butadiene Organic Syntheses. 82: 43-54. |
1 |
|
| 2005 |
Marshall JA, Yanik MM, Adams ND, Ellis KC, Chobanian HR. Generation of nonracemic 2-(tbutyldimethylsilyloxy)-3-butynyllithium from (S)ethyl lactate Organic Syntheses. 81. |
1 |
|
| 2004 |
Marshall JA, Eidam P. Diastereoselective additions of chiral vinylzinc reagents to alpha-chiral aldehydes. Organic Letters. 6: 445-8. PMID 14748614 DOI: 10.1021/ol0363568 |
1 |
|
| 2004 |
Marshall JA, Ellis K. Applications of chiral allenylzinc additions and Noyori asymmetric reductions to an enantioselective synthesis of a C3-C13 precursor of the polyketide phosphatase inhibitor cytostatin Tetrahedron Letters. 45: 1351-1353. DOI: 10.1016/j.tetlet.2003.12.067 |
1 |
|
| 2003 |
Marshall JA, Schaaf GM. Total synthesis and structure confirmation of leptofuranin D. The Journal of Organic Chemistry. 68: 7428-32. PMID 12968896 DOI: 10.1021/jo0348930 |
1 |
|
| 2003 |
Marshall JA, Bourbeau MP. Synthesis of enantioenriched propargylic alcohols related to polyketide natural products. A comparison of methodologies. Organic Letters. 5: 3197-9. PMID 12943386 DOI: 10.1021/ol034918h |
1 |
|
| 2003 |
Marshall JA, Chobanian HR. Synthesis of 2,5-disubstituted tetrahydrofurans by stereospecific elimination-cyclization of 1-iodomethyl-1,5-bis-epoxides. Organic Letters. 5: 1931-3. PMID 12762689 DOI: 10.1021/ol034509l |
1 |
|
| 2003 |
Marshall JA, Ellis KC. Total synthesis of (-)- and (+)-membrenone C. Organic Letters. 5: 1729-32. PMID 12735763 DOI: 10.1021/ol034367v |
1 |
|
| 2003 |
Marshall JA, Piettre A, Paige MA, Valeriote F. Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?). The Journal of Organic Chemistry. 68: 1780-5. PMID 12608791 DOI: 10.1021/jo0266137 |
1 |
|
| 2003 |
Marshall JA, Piettre A, Paige MA, Valeriote F. A modular synthesis of annonaceous acetogenins. The Journal of Organic Chemistry. 68: 1771-9. PMID 12608790 DOI: 10.1021/jo026433x |
1 |
|
| 2003 |
Gung BW, Xue X, Knatz N, Marshall JA. Addition of chiral allenylzinc reagent to acetaldehyde: Diastereotopic cyclic transition states with a tetrahedral zinc atom located by ab initio and density functional theory Organometallics. 22: 3158-3163. DOI: 10.1021/om030220w |
1 |
|
| 2003 |
Marshall JA, Bourbeau MP. Directed Pd(0)-catalyzed hydrostannations of internal alkynes Tetrahedron Letters. 44: 1087-1089. DOI: 10.1016/S0040-4039(02)02660-6 |
1 |
|
| 2002 |
Marshall JA, Bourbeau MP. Second-generation synthesis of the polypropionate subunit of callystatin A based on regioselective internal alkyne hydrostannation. Organic Letters. 4: 3931-4. PMID 12599495 DOI: 10.1021/ol026791m |
1 |
|
| 2002 |
Marshall JA, Bourbeau MP. Total synthesis of (-)-callystatin A. The Journal of Organic Chemistry. 67: 2751-4. PMID 11975524 DOI: 10.1021/jo016025d |
1 |
|
| 2002 |
Marshall JA, Adams ND. Total synthesis of bafilomycin V(1): a methanolysis product of the macrolide bafilomycin C(2). The Journal of Organic Chemistry. 67: 733-40. PMID 11856013 DOI: 10.1021/jo015864x |
1 |
|
| 2002 |
Johns BA, Grant CM, Marshall JA, Holson EB, Roush WR. Synthesis and utilization of indium (i) iodide for in situ formation of enantioenriched allenylindium reagents and their addition to aldehydes: (2r,3s,4s)-1-(tertbutyldiphenylsilyloxy)-2,4-dimethyl-5-hexyn-3-ol Organic Syntheses. 79: 59-70. |
1 |
|
| 2001 |
Marshall JA, Chobanian HR, Yanik MM. Coupling of alkynylTMS derivatives with vinylic iodides. An efficient route to 1,3-enynes and dienes. Organic Letters. 3: 4107-10. PMID 11735596 DOI: 10.1021/ol016899m |
1 |
|
| 2001 |
Marshall JA, Van Devender EA. Synthesis of (-)-deoxypukalide, the enantiomer of a degradation product of the furanocembranolide pukalide. The Journal of Organic Chemistry. 66: 8037-41. PMID 11722202 DOI: 10.1021/jo016048s |
1 |
|
| 2001 |
Marshall JA, Schaaf GM. Synthesis of stereopentad analogues of the C14-C22 segment of callystatin A through additions of chiral allenylzinc reagents to stereotriads. The Journal of Organic Chemistry. 66: 7825-31. PMID 11701042 DOI: 10.1021/jo015936k |
1 |
|
| 2001 |
Marshall JA, Chobanian HR, Yanik MM. Lipase-mediated resolution of 4-TMS-3-butyn-2-ol and use of the mesylate derivatives as a precursor to a highly stereoselective chiral allenylindium reagent. Organic Letters. 3: 3369-72. PMID 11594836 DOI: 10.1021/ol016605x |
1 |
|
| 2001 |
Marshall JA, Yanik MM. Synthesis of a C1-C21 subunit of the protein phosphatase inhibitor tautomycin: a formal total synthesis. The Journal of Organic Chemistry. 66: 1373-9. PMID 11312969 DOI: 10.1021/jo0056951 |
1 |
|
| 2001 |
Marshall JA, Gill K. The BF3 and B(C6F5)3-catalyzed 1,3-isomerization of allylic stannanes Journal of Organometallic Chemistry. 624: 294-299. DOI: 10.1016/S0022-328X(01)00642-8 |
1 |
|
| 2001 |
Cossy J, Rasamison C, Pardo DG, Marshall JA. Solid-support synthesis of 1,2-diols and γ-lactones through addition of α-(benzoyloxy)crotylindium reagents to aldehydes Synlett. 629-633. |
1 |
|
| 2000 |
Marshall JA, Chobanian HR. Additions of enantioenriched allenylzinc and indium reagents to lactic aldehyde ethers The Journal of Organic Chemistry. 65: 8357-60. PMID 11101396 |
0.96 |
|
| 2000 |
Marshall JA, Adams ND. Progress toward the total synthesis of bafilomycin A(1): stereoselective synthesis of the C15-C25 subunit by additions of nonracemic allenylzinc reagents to aldehydes. Organic Letters. 2: 2897-900. PMID 10964393 |
1 |
|
| 2000 |
Marshall JA, Yanik MM. Synthesis of beta-hydroxy ketones and vinylsilanes from homopropargylic alcohols by intramolecular hydrosilation Organic Letters. 2: 2173-5. PMID 10891259 |
1 |
|
| 2000 |
Marshall JA, Johns BA. Stereoselective synthesis of C5-C20 and C21-C34 subunits of the core structure of the aplyronines. Applications of enantioselective additions of chiral allenylindium reagents to chiral aldehydes. The Journal of Organic Chemistry. 65: 1501-10. PMID 10814114 DOI: 10.1021/jo991689x |
1 |
|
| 2000 |
Marshall JA, Maxson K. Stereoselective synthesis of stereotriad subunits of polyketides through additions of nonracemic allenylsilanes to (R)- and (S)-2-methyl-3-oxygenated propanals The Journal of Organic Chemistry. 65: 630-3. PMID 10813988 DOI: 10.1021/jo991543y |
1 |
|
| 2000 |
Marshall JA, Gill K, Seletsky BM. Addition of Enantioenriched gamma-Oxygenated Allylic Stannanes to N-Acyl Iminium Intermediates: A New Synthesis of syn-Amino Alcohol Derivatives This research was supported by the National Institute of Allergy and Infectious Diseases (grant R01 AI31422). Angewandte Chemie (International Ed. in English). 39: 953-956. PMID 10760905 DOI: 10.1002/(SICI)1521-3773(20000303)39:5<953::AID-ANIE953>3.0.CO;2-I |
1 |
|
| 2000 |
Marshall JA, Chobanian HR. Additions of enantioenriched alenylzinc and indium reagents to lactic aldehyde ethers Journal of Organic Chemistry. 65: 8357-8360. DOI: 10.1021/jo005658+ |
1 |
|
| 2000 |
Marshall JA. Synthesis and reactions of allylic, allenic, vinylic, and arylmetal reagents from halides and esters via transient organopalladium intermediates Chemical Reviews. 100: 3163-3185. DOI: 10.1021/cr000003u |
1 |
|
| 2000 |
Marshall JA, Zou D. A new synthesis of 3-carboxy-2,5-disubstituted furans and their conversion to 5-vinyl derivatives Tetrahedron Letters. 41: 1347-1350. DOI: 10.1016/S0040-4039(99)02290-X |
1 |
|
| 2000 |
Marshall JA. Rhodium-catalyzed reformatsky-type reaction Chemtracts. 13: 705-707. |
1 |
|
| 2000 |
Marshall JA, Garofalo AW, Hinkle KW. Synthesis of (S,E)-1-(methoxymethoxy)-1-tributylstannyl-2-bytene: (Stannane, tributyl[1-(methoxymethoxy)-2-butenyl]-, [S-(E)]-) Organic Syntheses. 77: 98-105. |
1 |
|
| 2000 |
Marshall JA, Yanik MM. Synthesis of β-hydroxy ketones and vinylsilanes from homopropargylic alcohols by intramolecular hydrosilation Organic Letters. 2: 2173-2175. |
1 |
|
| 2000 |
Marshall JA, Yanik MM. Stereoselective synthesis of substituted ketopyranose subunits of polyketide natural products by intramolecular alkoxycarbonylation of δ- alkynyl alcohols Tetrahedron Letters. 41: 4717-4721. |
1 |
|
| 2000 |
Marshall JA. Umpolung of chiral 2-ethynylaziridines: Indium(I)-mediated stereoselective synthesis of nonracemic 1,3-amino alcohols bearing three chiral centers, catalyzed by palladium(0) Chemtracts. 13: 616-619. |
1 |
|
| 2000 |
Marshall JA. Oxidative transmetalation as a route to allylboronates and in situ allylboranes from allylic halides and alcohols Chemtracts. 13: 612-615. |
1 |
|
| 2000 |
Marshall JA. Pd-catalyzed borylation of aryl halides Chemtracts. 13: 219-222. |
1 |
|
| 1999 |
Marshall JA, Grant CM. Preparation of Chiral Allenylmetal Reagents from Enantioenriched Allenyl Iodides and Propargylic Mesylates. A Comparison of Indium, Bismuth, and Tin Derivatives. The Journal of Organic Chemistry. 64: 8214-8219. PMID 11674739 DOI: 10.1021/jo990938e |
1 |
|
| 1999 |
Marshall JA, Jablonowski JA, Jiang H. Total Synthesis of the Gypsy Moth Pheromones (+)- and (-)-Disparlure from a Single Nonracemic alpha-Silyloxy Allylic Stannane. The Journal of Organic Chemistry. 64: 2152-2154. PMID 11674319 |
1 |
|
| 1999 |
Marshall JA, Jiang H. Total Synthesis of the Cytotoxic Threo, Trans, Erythro, Cis, Threo Annonaceous Acetogenin Trilobin. The Journal of Organic Chemistry. 64: 971-975. PMID 11674171 DOI: 10.1021/jo982057y |
1 |
|
| 1999 |
Marshall JA, Grant CM. Formation of Transient Chiral Allenylindium Reagents from Enantioenriched Propargylic Mesylates through Oxidative Transmetalation. Applications to the Synthesis of Enantioenriched Homopropargylic Alcohols. The Journal of Organic Chemistry. 64: 696-697. PMID 11674133 DOI: 10.1021/jo982255p |
1 |
|
| 1999 |
Marshall JA, Jiang H. Total synthesis of the cytotoxic threo, trans, threo, trans, threo annonaceous acetogenin asimin and its C-10 epimer: unambiguous confirmation of absolute stereochemistry. Journal of Natural Products. 62: 1123-7. PMID 10479317 DOI: 10.1021/np990132+ |
1 |
|
| 1999 |
Marshall JA, Yanik MM. Synthesis of nonracemic β-hydroxy ketones and carbonate derivatives from homopropargylic alcohols through iodolactonization Journal of Organic Chemistry. 64: 3798-3799. DOI: 10.1021/jo990439d |
1 |
|
| 1999 |
Marshall JA, McNulty LM, Zou D. Synthesis of pseudopterane analogues by intramolecular S(E)2' cyclization Journal of Organic Chemistry. 64: 5193-5200. DOI: 10.1021/jo990376z |
1 |
|
| 1999 |
Marshall JA, Fitzgerald RN. Synthesis of a syn,syn,syn,syn-stereopentad precursor of the marine sponge polyketide callystatin A Journal of Organic Chemistry. 64: 4477-4481. DOI: 10.1021/jo9902143 |
1 |
|
| 1999 |
Marshall JA, Jablonowski JA, Jiang H. Total synthesis of the gypsy moth pheromones (+)- and (-)-disparlure from a single nonracemic α-silyloxy allylic stannane Journal of Organic Chemistry. 64: 2152-2154. DOI: 10.1021/jo982353a |
1 |
|
| 1999 |
Marshall JA, Adams ND. Addition of allenylzinc reagents, prepared in situ from nonracemic propargylic mesylates, to aldehydes. A new synthesis of highly enantioenriched homopropargylic alcohols Journal of Organic Chemistry. 64: 5201-5204. DOI: 10.1021/jo9823083 |
1 |
|
| 1999 |
Marshall JA, Sehon CA. Isomerization of β-alkynyl allylic alcohols to furans catalyzed by silver nitrate on silica gel: 2-pentyl-3-methyl-5-heptylfuran Organic Syntheses. 76: 263-269. |
1 |
|
| 1998 |
Marshall JA, Jiang H. Total Synthesis of the Nonadjacent Bis-Tetrahydrofuran Annonaceous Acetogenin Squamostatin-D. The Journal of Organic Chemistry. 63: 7066-7071. PMID 11672333 DOI: 10.1021/jo981103r |
1 |
|
| 1998 |
Marshall JA, Liao J. Stereoselective Total Synthesis of the Pseudopterolide Kallolide A. The Journal of Organic Chemistry. 63: 5962-5970. PMID 11672200 DOI: 10.1021/jo980603h |
1 |
|
| 1998 |
Marshall JA, Lu ZH, Johns BA. Synthesis of Discodermolide Subunits by S(E)2' Addition of Nonracemic Allenylstannanes to Aldehydes. The Journal of Organic Chemistry. 63: 817-823. PMID 11672079 |
0.52 |
|
| 1998 |
Marshall JA, Johns BA. Total synthesis of (+)-discodermolide Journal of Organic Chemistry. 63: 7885-7892. DOI: 10.1021/jo9811423 |
1 |
|
| 1998 |
Marshall JA, Jiang H. Total synthesis of the threo, trans, threo-mono-tetrahydrofuran annonaceous acetogenin longifolicin Tetrahedron Letters. 39: 1493-1496. DOI: 10.1016/S0040-4039(98)00007-0 |
1 |
|
| 1998 |
Marshall JA, Hinkle KW. Total synthesis of the cytotoxic annonaceous acetogenin (30S)-bullanin Tetrahedron Letters. 39: 1303-1306. DOI: 10.1016/S0040-4039(97)10739-0 |
1 |
|
| 1998 |
Marshall JA. Organic chemistry of Bi(III) compounds Chemtracts. 10: 1073-1075. |
1 |
|
| 1998 |
Marshall JA. Stereo- and enantioselective additions of allylic, propargylic, and allenic trihalosilanes to aldehydes Chemtracts. 11: 697-712. |
1 |
|
| 1998 |
Marshall JA, Palovich MR. Enantioselective and Diastereoselective Additions of Allylic Stannanes to Aldehydes Promoted by a Chiral (Acyloxy)borane Catalyst Journal of Organic Chemistry. 63: 4381-4384. |
1 |
|
| 1998 |
Marshall JA, Adams ND. Synthesis of Chiral Enantioenriched Homopropargylic Alcohols from Propargylic Mesylates via Chiral Allenylzinc Intermediates Journal of Organic Chemistry. 63: 3812-3813. |
1 |
|
| 1998 |
Marshall JA, Palovich MR. Synthesis of Stereopentad Subunits of Zincophorin and Rifamycin-S through Use of Chiral Allenyltin Reagents Journal of Organic Chemistry. 63: 3701-3705. |
1 |
|
| 1998 |
Marshall JA, Lu ZH, Johns BA. Synthesis of Discodermolide Subunits by SE2′ Addition of Nonracemic Allenylstannanes to Aldehydes Journal of Organic Chemistry. 63: 817-823. |
1 |
|
| 1998 |
Marshall JA. A novel method for inside selective silylation of 1,2-diols Chemtracts. 11: 828-831. |
1 |
|
| 1998 |
Marshall JA. Catalytic asymmetric allylation of imines via chiral bis-pi- allylpalladium complexes Chemtracts. 11: 855-858. |
1 |
|
| 1997 |
Marshall JA, Sehon CA. Total Synthesis of the Enantiomer of the Furanocembrane Rubifolide. The Journal of Organic Chemistry. 62: 4313-4320. PMID 11671752 DOI: 10.1021/jo970360d |
1 |
|
| 1997 |
Marshall JA, Wolf MA, Wallace EM. Synthetic Routes to Allenic Acids and Esters and Their Stereospecific Conversion to Butenolides. The Journal of Organic Chemistry. 62: 367-371. PMID 11671411 |
1 |
|
| 1997 |
Marshall JA, Hinkle KW. Total synthesis of the Annonaceous acetogenin (+)-asimicin. Development of a new bidirectional strategy Journal of Organic Chemistry. 62: 5989-5995. DOI: 10.1021/jo970423s |
1 |
|
| 1997 |
Marshall JA, Chen M. Total Synthesis of the Annonaceous Acetogenins Asiminocin and Asiminecin by a Bidirectional Approach Journal of Organic Chemistry. 62: 5996-5997. |
1 |
|
| 1997 |
Marshall JA. Direct preparation of allylstannanes from allylic alcohols: Convenient synthesis of β-substituted allylstannanes. Ti IV binolate-catalyzed highly enantioselective additions of β-substituted allylstannanes to aldehydes Chemtracts. 10: 649-652. |
1 |
|
| 1997 |
Marshall JA, Hinkle KW, Hagedorn CE. Recent developments in the synthesis of annonaceous acetogenins Israel Journal of Chemistry. 37: 97-107. |
1 |
|
| 1997 |
Marshall JA, Palovich MR. Comparative Studies on the Synthesis of an anti,syn Stereotriad with Chiral Allenylstannane and Allenylindium Reagents Journal of Organic Chemistry. 62: 6001-6005. |
1 |
|
| 1997 |
Marshall JA. Additions of allylic indium reagents to aldehydes Chemtracts. 10: 481-496. |
1 |
|
| 1996 |
Marshall JA. Chiral Allylic and Allenic Stannanes as Reagents for Asymmetric Synthesis. Chemical Reviews. 96: 31-48. PMID 11848743 |
1 |
|
| 1996 |
Marshall JA, Hinkle KW. Stereoselective S(E)2' Additions of Enantioenriched Allylic Tin and Indium Reagents to Protected Threose and Erythrose Aldehydes: A General Strategy for the Stereocontrolled Synthesis of Precursors to the Eight Diastereomeric Hexoses and Their Enantiomers. The Journal of Organic Chemistry. 61: 9072. PMID 11667908 |
0.92 |
|
| 1996 |
Marshall JA, Garofalo AW. Synthesis of Chiral alpha,delta-Dioxygenated Allylic Stannanes as Reagents for Carbohydrate Synthesis and Homologation. The Journal of Organic Chemistry. 61: 8732-8738. PMID 11667845 |
0.64 |
|
| 1996 |
Marshall JA, Elliott LM. Methyl 2,3,4-Tri-O-benzyl-alpha-D-glucopyranosyl-Derived gamma-Silyloxy Allylic Stannanes as Reagents for S(E)2' Additions to Aldehydes. The Journal of Organic Chemistry. 61: 4611-4616. PMID 11667388 |
0.32 |
|
| 1996 |
Marshall JA, Hinkle KW. An Efficient Bidirectional Approach to the C(2)-Symmetric Stereoisomers of the Bistetrahydrofuran Core of the Acetogenins. The Journal of Organic Chemistry. 61: 4247-4251. PMID 11667322 |
0.92 |
|
| 1996 |
Marshall JA, Jablonowski JA, Welmaker GS. On the Relative Reactivities of Allyl, Crotyl, alpha-Oxygenated Crotyl, gamma-Oxygenated alpha-Methylallyl, and Allenyl Tri-n-butylstannane Reagents in Lewis Acid Promoted Additions to Aldehydes. The Journal of Organic Chemistry. 61: 2904-2907. PMID 11667135 |
0.88 |
|
| 1996 |
Marshall JA, Beaudoin S. Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. The Journal of Organic Chemistry. 61: 581-586. PMID 11666978 DOI: 10.1021/jo9517914 |
1 |
|
| 1996 |
Marshall JA, Bartley GS, Wallace EM. Total synthesis of the pseudopterane (-)-kallolide B, the enantiomer of natural (+)-kallolide B Journal of Organic Chemistry. 61: 5729-5735. DOI: 10.1021/jo960798y |
1 |
|
| 1996 |
Marshall JA, Wolf MA. Amination, aminocarbonylation, and alkoxycarbonylation of allenic/propargylic Pd intermediates derived from nonracemic propargylic mesylates: Synthesis of nonracemic propargyl amines, allenic amides, and butenolides Journal of Organic Chemistry. 61: 3238-3239. DOI: 10.1021/jo960442m |
1 |
|
| 1996 |
Marshall JA, Hinkle KW. An efficient bidirectional approach to the C2-symmetric stereoisomers of the bistetrahydrofuran core of the acetogenins Journal of Organic Chemistry. 61: 4247-4251. DOI: 10.1021/jo9603789 |
1 |
|
| 1996 |
Marshall JA, Garofalo AW. Synthesis of Chiral α,δ-Dioxygenated Allylic Stannanes as Reagents for Carbohydrate Synthesis and Homologation Journal of Organic Chemistry. 61: 8732-8738. |
1 |
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| 1996 |
Marshall JA, Xie S. Observations on an iodocarbonate route to certain 1,3-diols related to the C22-34 subunit of FK-506 Journal of the Brazilian Chemical Society. 7: 225-230. |
1 |
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| 1996 |
Marshall JA, Elliott LM. Methyl 2,3,4-Tri-O-benzyl-α-D-glucopyranosyl-derived γ-silyloxy allylic stannanes as reagents for SE2′ additions to aldehydes Journal of Organic Chemistry. 61: 4611-4616. |
1 |
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| 1996 |
Marshall JA, Jablonowski JA, Welmaker GS. On the relative reactivities of allyl, crotyl, α-oxygenated crotyl, γ-oxygenated α-methylallyl, and allenyl tri-n-butylstannane reagents in Lewis acid promoted additions to aldehydes Journal of Organic Chemistry. 61: 2904-2907. |
1 |
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| 1996 |
Marshall JA, Hinkle KW. Stereoselective SE2′ additions of enantioenriched allylic tin and indium reagents to protected threose and erythrose aldehydes: A general strategy for the stereocontrolled synthesis of precursors to the eight diastereomeric hexoses and their enantiomers Journal of Organic Chemistry. 61: 105-108. |
1 |
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| 1995 |
Marshall JA, Yu RH, Perkins JF. Diastereo- and enantioselective synthesis of allenylcarbinols through SE2′ addition of transient nonracemic propargylic stannanes to aldehydes The Journal of Organic Chemistry. 60: 5550-5555. |
1 |
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| 1995 |
Marshall JA, Wallace EM, Coan PS. Total synthesis of the pseudopterane (±)-kallolide B The Journal of Organic Chemistry. 60: 796-797. |
1 |
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| 1995 |
Marshall JA, Hinkle KW. Synthesis of anti-homoallylic alcohols and monoprotected 1,2-diols through InCl3-promoted addition of allylic stannanes to aldehydes Journal of Organic Chemistry. 60: 1920-1921. |
1 |
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| 1995 |
Marshall JA, Perkins JF, Wolf MA. Synthesis of syn,syn; anti,syn; syn,anti; and anti,anti stereotriads from a single pair of enantiomeric reagents The Journal of Organic Chemistry. 60: 5556-5559. |
1 |
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| 1995 |
Marshall JA, Jablonowski JA, Elliott LM. Interconversion of nonracemic α-OTBS crotyl and γ-OTBS methallyl tri-n-butylstannanes. Additions of the (E)-methallyl isomer to representative aldehydes Journal of Organic Chemistry. 60: 2662-2663. |
1 |
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| 1986 |
Marshall JA, Audia VH, Jenson TM, Guida WC. Jump rope rotation in trans-cycloalkenes Tetrahedron. 42: 1703-1709. DOI: 10.1016/S0040-4020(01)87587-6 |
1 |
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| 1974 |
Marshall JA, Brady SF, Andersen NH. The chemistry of spiro(4.5)decane sesquiterpenes. Fortschritte Der Chemie Organischer Naturstoffe = Progress in the Chemistry of Organic Natural Products. ProgrèS Dans La Chimie Des Substances Organiques Naturelles. 31: 283-376. PMID 4609864 |
0.4 |
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| 1969 |
Marshall JA, Brady SF. Stereochemical relationships in spirovetivane sesquiterpenes: the total synthesis of hinesol. Tetrahedron Letters. 1387-90. PMID 5794433 DOI: 10.1016/S0040-4039(01)87894-1 |
0.4 |
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| 1966 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. VII. The synthesis of (+or-)-8-beta-carbomethoxy-13-oxopodocarpanone, a degradation product of phyllocladene. The Journal of Organic Chemistry. 31: 2526-30. PMID 5917441 DOI: 10.1021/jo01346a023 |
1 |
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| 1962 |
Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. III. The use of trans-Δ6-octalone-1 in the preparation of dicyclic intermediates Journal of Organic Chemistry. 27: 1620-1627. DOI: 10.1021/jo01052a032 |
1 |
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| 1962 |
Ireland RE, Marshall JA. The n-butylthiomethylene blocking group Journal of Organic Chemistry. 27: 1615-1619. DOI: 10.1021/jo01052a031 |
1 |
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| 1962 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. II. The synthesis of dl-6-keto-5,5,9-trimethyl-2-methylene-trans-decalyl-1α-acetic acid and derivatives Journal of Organic Chemistry. 27: 1118-1125. DOI: 10.1021/jo01051a002 |
1 |
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| 1961 |
Church RF, Ireland RE, Marshall JA. A novel approach to a key intermediate in the total synthesis of α-onocerin Tetrahedron Letters. 2: 34-38. DOI: 10.1016/S0040-4039(01)99201-9 |
1 |
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| 1960 |
Church RF, Ireland RE, Marshall JA. The stereospecific total synthesis of d1-8β-carbomethoxy-13-oxopodocarpane, a degradation product of phyllocladene Tetrahedron Letters. 1: 1-4. DOI: 10.1016/S0040-4039(01)99337-2 |
1 |
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| 1959 |
Ireland RE, Marshall JA. The n-butylthiomethylene grouping: A superior blocking group for the alkylation of ketones [12] Journal of the American Chemical Society. 81: 6336-6337. DOI: 10.1021/ja01532a064 |
1 |
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| 1959 |
Ireland RE, Marshall JA. A new synthetic method for the preparation of α-substituted β-ketoesters [4] Journal of the American Chemical Society. 81: 2907-2908. DOI: 10.1021/ja01520a073 |
1 |
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