| Year |
Citation |
Score |
| 2016 |
Wada K, Sakai M, Kawashima H, Ogawa N, Kobayashi Y. Efficient Synthesis of Anastrephin via the Allylic Substitution for Quaternary Carbon Construction Synlett. 27: 1428-1432. DOI: 10.1055/s-0035-1561576 |
0.332 |
|
| 2012 |
Paudel A, Hamamoto H, Kobayashi Y, Yokoshima S, Fukuyama T, Sekimizu K. Identification of novel deoxyribofuranosyl indole antimicrobial agents. The Journal of Antibiotics. 65: 53-7. PMID 22167161 DOI: 10.1038/Ja.2011.110 |
0.674 |
|
| 2010 |
Gilley CB, Buller MJ, Kobayashi Y. ChemInform Abstract: Synthesis of Proteasome Inhibitor Omuralide Featuring Stereocontrolled Ugi Reaction and Novel Convertible Isocyanide Cheminform. 41. DOI: 10.1002/chin.201018239 |
0.789 |
|
| 2010 |
Kobayashi Y, Fujimoto T, Fukuyama T. ChemInform Abstract: Stereocontrolled Total Synthesis of (+)-K252a. Cheminform. 30: no-no. DOI: 10.1002/chin.199944247 |
0.566 |
|
| 2009 |
Isaacson J, Kobayashi Y. An Ugi reaction in the total synthesis of (-)-dysibetaine. Angewandte Chemie (International Ed. in English). 48: 1845-8. PMID 19173271 DOI: 10.1002/anie.200805709 |
0.392 |
|
| 2009 |
Gilley CB, Buller MJ, Kobayashi Y. Synthesis of proteasome inhibitor omuralide featuring stereocontrolled Ugi reaction and novel convertible isocyanide Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 67: 1183-1193. DOI: 10.5059/Yukigoseikyokaishi.67.1183 |
0.815 |
|
| 2009 |
Vamos M, Kobayashi Y. Propellane as a conformational device for the stabilization of the β-lactone of salinosporamide A Tetrahedron. 65: 5899-5903. DOI: 10.1016/J.Tet.2009.05.085 |
0.797 |
|
| 2009 |
Gilley CB, Buller MJ, Kobayashi Y. ChemInform Abstract: Synthesis of Functionalized Pyroglutamic Acids. Part 2. The Stereoselective Condensation of Multifunctional Groups with Chiral Levulinic Acids. Cheminform. 40. DOI: 10.1002/chin.200904102 |
0.796 |
|
| 2009 |
Buller MJ, Gilley CB, Nguyen B, Olshansky L, Fraga B, Kobayashi Y. ChemInform Abstract: Synthesis of Functionalized Pyroglutamic Acids. Part 1. The Synthetic Utility of N-Acylindole and the Ugi Reaction with a Chiral Levulinic Acid. Cheminform. 40. DOI: 10.1002/chin.200904101 |
0.81 |
|
| 2008 |
Nguyen TX, Kobayashi Y. Synthesis of the common propellane core structure of the hasubanan alkaloids. The Journal of Organic Chemistry. 73: 5536-41. PMID 18549291 DOI: 10.1021/Jo800793S |
0.45 |
|
| 2008 |
Gilley CB, Kobayashi Y. 2-nitrophenyl isocyanide as a versatile convertible isocyanide: rapid access to a fused gamma-lactam beta-lactone bicycle. The Journal of Organic Chemistry. 73: 4198-204. PMID 18459807 DOI: 10.1021/Jo800486K |
0.772 |
|
| 2008 |
Vamos M, Kobayashi Y. Scalable preparation of both enantiomers of 2-(1-hydroxy-2-oxocyclohexyl)acetic acid. The Journal of Organic Chemistry. 73: 3938-41. PMID 18416575 DOI: 10.1021/Jo8000904 |
0.799 |
|
| 2008 |
Isaacson J, Loo M, Kobayashi Y. Total synthesis of (+/-)-dysibetaine. Organic Letters. 10: 1461-3. PMID 18318540 DOI: 10.1021/Ol800245M |
0.499 |
|
| 2008 |
Gilley CB, Buller MJ, Kobayashi Y. Synthesis of functionalized pyroglutamic acids, part 2: The stereoselective condensation of multifunctional groups with chiral levulinic acids Synlett. 2249-2252. DOI: 10.1055/S-2008-1078211 |
0.81 |
|
| 2008 |
Buller MJ, Gilley CB, Nguyen B, Olshansky L, Fraga B, Kobayashi Y. Synthesis of functionalized pyroglutamic acids, part 1: The synthetic utility of N-acylindole and the ugi reaction with a chiral levulinic acid Synlett. 2244-2248. DOI: 10.1055/S-2008-1078173 |
0.812 |
|
| 2008 |
Kobayashi Y, Born S. A Stable Synthetic Equivalent
of 2,3-Dihydropyridine Synlett. 2008: 2479-2482. DOI: 10.1055/S-2008-1078056 |
0.793 |
|
| 2008 |
Kobayashi Y, Born S, Bacani G, Olson E. Microwave-Assisted Intramolecular
Diels-Alder Reaction towards the Total Synthesis of Symbioimine Synlett. 2008: 2877-2881. DOI: 10.1055/S-0028-1083501 |
0.793 |
|
| 2008 |
Gilley CB, Kobayashi Y. ChemInform Abstract: 2-Nitrophenyl Isocyanide as a Versatile Convertible Isocyanide: Rapid Access to a Fused γ-Lactam β-Lactone Bicycle. Cheminform. 39. DOI: 10.1002/chin.200841120 |
0.733 |
|
| 2007 |
Gilley CB, Buller MJ, Kobayashi Y. New entry to convertible isocyanides for the Ugi reaction and its application to the stereocontrolled formal total synthesis of the proteasome inhibitor omuralide. Organic Letters. 9: 3631-4. PMID 17672474 DOI: 10.1021/Ol701446Y |
0.805 |
|
| 2007 |
Isaacson J, Gilley CB, Kobayashi Y. Expeditious access to unprotected racemic pyroglutamic acids. The Journal of Organic Chemistry. 72: 3913-6. PMID 17417909 DOI: 10.1021/Jo0700225 |
0.801 |
|
| 2007 |
Buller MJ, Cook TG, Kobayashi Y. Versatile Synthesis of 2,2-Disubstituted Indolinones via Protected Indolones Generated by One-Pot Multi-Oxidation of 2-Substituted Indoles. Cheminform. 38. DOI: 10.3987/Com-06-S(K)39 |
0.7 |
|
| 2007 |
Vamos M, Ozboya K, Kobayashi Y. Synthesis of bicyclic pyroglutamic acid featuring the ugi reaction and a unique stereoisomerization at the angular position by Grob fragmentation followed by a transannular ketene [2+2] cycloaddition reaction Synlett. 1595-1599. DOI: 10.1055/S-2007-982538 |
0.814 |
|
| 2003 |
Higashibayashi S, Czechtizky W, Kobayashi Y, Kishi Y. Universal NMR databases for contiguous polyols. Journal of the American Chemical Society. 125: 14379-93. PMID 14624586 DOI: 10.1021/Ja0375481 |
0.553 |
|
| 2003 |
Kobayashi Y, Czechtizky W, Kishi Y. Complete stereochemistry of tetrafibricin. Organic Letters. 5: 93-6. PMID 12509899 DOI: 10.1021/Ol0272895 |
0.597 |
|
| 2003 |
Kobayashi Y, Hayashi N, Kishi Y. Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: Scope and limitation Tetrahedron Letters. 44: 7489-7491. DOI: 10.1016/J.Tetlet.2003.08.022 |
0.567 |
|
| 2002 |
Kobayashi Y, Hayashi N, Kishi Y. Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols. Organic Letters. 4: 411-4. PMID 11820892 DOI: 10.1021/Ol0171160 |
0.583 |
|
| 2001 |
Kobayashi Y, Tan CH, Kishi Y. Toward creation of a universal NMR database for stereochemical assignment: complete structure of the desertomycin/oasomycin class of natural products. Journal of the American Chemical Society. 123: 2076-8. PMID 11456839 DOI: 10.1021/Ja004154Q |
0.652 |
|
| 2001 |
Kobayashi Y, Hayashi N, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: NMR desymmetrization of meso compounds. Organic Letters. 3: 2253-5. PMID 11440592 DOI: 10.1021/Ol010110Q |
0.595 |
|
| 2001 |
Hayashi N, Kobayashi Y, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: scope and limitation. Organic Letters. 3: 2249-52. PMID 11440591 DOI: 10.1021/Ol010109R |
0.619 |
|
| 2001 |
Kobayashi Y, Hayashi N, Tan CH, Kishi Y. Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept. Organic Letters. 3: 2245-8. PMID 11440590 DOI: 10.1021/Ol010108Z |
0.685 |
|
| 2000 |
Kobayashi Y, Tan CH, Kishi Y. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Prediction. Angewandte Chemie (International Ed. in English). 39: 4279-4281. PMID 29711895 DOI: 10.1002/1521-3773(20001201)39:23<4279::Aid-Anie4279>3.0.Co;2-R |
0.591 |
|
| 2000 |
Tan CH, Kobayashi Y, Kishi Y. Stereochemical Assignment of the C21-C38 Portion of the Desertomycin/Oasomycin Class of Natural Products by Using Universal NMR Databases: Proof. Angewandte Chemie (International Ed. in English). 39: 4282-4284. PMID 29711890 DOI: 10.1002/1521-3773(20001201)39:23<4282::AID-ANIE4282>3.0.CO;2-U |
0.536 |
|
| 2000 |
Numano F, Kishi Y, Tanaka A, Ohkawara M, Kakuta T, Kobayashi Y. Inflammation and atherosclerosis. Atherosclerotic lesions in Takayasu arteritis. Annals of the New York Academy of Sciences. 902: 65-76. PMID 10865826 |
0.489 |
|
| 2000 |
Kobayashi Y, Tan CH, Kishi Y. Toward creation of a universal NMR database for stereochemical assignment: The case of 1,3,5-trisubstituted acyclic systems Helvetica Chimica Acta. 83: 2562-2571. DOI: 10.1002/1522-2675(20000906)83:9<2562::Aid-Hlca2562>3.0.Co;2-Z |
0.67 |
|
| 2000 |
Tan CH, Kobayashi Y, Kishi Y. Stereochemical assignment of the C21 - C38 portion of the desertomycin/oasomycin class of natural products by using universal NMR databases: Proof Angewandte Chemie - International Edition. 39: 4282-4284. DOI: 10.1002/1521-3773(20001201)39:23<4282::AID-ANIE4282>3.0.CO;2-U |
0.439 |
|
| 2000 |
Kobayashi Y, Tan CH, Kishi Y. Stereochemical assignment of the C21-C38 portion of the desertomycin/oasomycin class of natural products by using universal NMR databases: Prediction Angewandte Chemie - International Edition. 39: 4279-4281. DOI: 10.1002/1521-3773(20001201)39:23<4279::AID-ANIE4279>3.0.CO;2-R |
0.434 |
|
| 1999 |
Lee J, Kobayashi Y, Tezuka K, Kishi Y. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: proof of concept. Organic Letters. 1: 2181-4. PMID 10836073 DOI: 10.1021/Ol990379Y |
0.611 |
|
| 1999 |
Kobayashi Y, Lee J, Tezuka K, Kishi Y. Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: the case of two contiguous propionate units. Organic Letters. 1: 2177-80. PMID 10836072 DOI: 10.1021/Ol9903786 |
0.601 |
|
| 1999 |
Kobayashi Y, Fujimoto T, Fukuyama T. Stereocontrolled Total Synthesis of (+)-K252a Journal of the American Chemical Society. 121: 6501-6502. DOI: 10.1021/Ja990909L |
0.718 |
|
| 1998 |
Moncada G, Kobayashi Y, Kaneko E, Nishiwaki Y, Kishi Y, Numano F. Subclavian steal syndrome secondary to Takayasu arteritis. International Journal of Cardiology. 66: S231-6. PMID 9951824 |
0.495 |
|
| 1998 |
Moncada G, Kobayashi Y, Maruyama Y, Kato T, Noda M, Kakuta T, Kishi Y, Numano F. Long-term patency of an aorta-aortic graft bypass in a patient with Takayasu arteritis. Internal Medicine (Tokyo, Japan). 37: 934-9. PMID 9868955 |
0.482 |
|
| 1998 |
Kobayashi Y, Fukuyama T. Development of a novel indole synthesis and its application to natural products synthesis Journal of Heterocyclic Chemistry. 35: 1043-1056. DOI: 10.1002/Jhet.5570350504 |
0.632 |
|
| 1996 |
Numano F, Kobayashi Y, Maruyama Y, Kakuta T, Miyata T, Kishi Y. Takayasu arteritis: clinical characteristics and the role of genetic factors in its pathogenesis. Vascular Medicine (London, England). 1: 227-33. PMID 9546941 |
0.471 |
|
| 1973 |
Kobayashi Y, Komiya I, Utsuno Y, Kishi Y, Hayashi Y. [Symposium. Our methods in public health nursing]. [Hokenfu Zasshi] the Japanese Journal For Public Health Nurse. 29: 698-711. PMID 4491700 |
0.472 |
|
| 1973 |
Kobayashi Y, Komiya I, Utsuno Y, Kishi Y, Hayashi Y. [Symposium. Our methods in public health nursing activities]. [Hokenfu Zasshi] the Japanese Journal For Public Health Nurse. 29: 774-83. PMID 4491179 |
0.472 |
|
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