| Year |
Citation |
Score |
| 2023 |
Shiina I, Iizumi T, Taniguchi S, Sugimoto M, Shimazaki T, Yamai YS, Ogawa G, Yamada T, Shinohara S, Kageyama Y, Kuboki T, Suwa Y, Yonekura K, Ito K, Toyoyama K, et al. Total Synthesis of the Sesquiterpene (-)-Merrillianin. Organic Letters. PMID 38160411 DOI: 10.1021/acs.orglett.3c03877 |
0.311 |
|
| 2023 |
Murata T, Tsutsui H, Yoshida T, Kubota H, Hiraishi S, Natsukawa H, Suzuki Y, Hiraga D, Mori T, Maekawa Y, Tateyama S, Toyoyama K, Ito K, Suzuki K, Yonekura K, ... ... Shiina I, et al. First Total Synthesis of Tanzawaic Acid B. Acs Omega. 8: 27703-27709. PMID 37546667 DOI: 10.1021/acsomega.3c03634 |
0.333 |
|
| 2019 |
Shiina I, Miesch M, Peter C, Geoffroy P, Murata T, Tonoi T. Diastereo–/Enantioselective Diels–Alder Synthesis of 14β-Hydroxysteroid Scaffolds: A Combined Experimental and DFT Study Heterocycles. 99: 1251. DOI: 10.3987/Com-18-S(F)99 |
0.371 |
|
| 2018 |
Murata T, Kuboki T, Ishikawa R, Saito T, Taguchi S, Takeuchi K, Hatano E, Shimonaka M, Shiina I. Total Synthesis of Violaceoid A and (-)- and (+)-Violaceoid B. Journal of Natural Products. PMID 30375869 DOI: 10.1021/Acs.Jnatprod.8B00215 |
0.398 |
|
| 2018 |
Murata T, Kawanishi T, Sekiguchi A, Ishikawa R, Ono K, Nakata K, Shiina I. Kinetic Resolution of Racemic 2-Hydroxyamides Using a Diphenylacetyl Component as an Acyl Source and a Chiral Acyl-Transfer Catalyst. Molecules (Basel, Switzerland). 23. PMID 30103468 DOI: 10.3390/Molecules23082003 |
0.403 |
|
| 2018 |
Tonoi T, Inohana T, Sato T, Yoshida T, Shiina I. Total Synthesis and Antimicrobial Activities of All Stereoisomers of (16Z,20E)-Eushearilide and (16E,20E)-Eushearilide. The Journal of Organic Chemistry. PMID 29847953 DOI: 10.1021/Acs.Joc.8B00774 |
0.336 |
|
| 2017 |
Tonoi T, Yoshinaga Y, Fujishiro M, Mameda K, Kato T, Shibamoto K, Shiina I. Asymmetric Total Synthesis of (-)-Astakolactin and Confirmation of Its Stereostructure. Journal of Natural Products. PMID 28767241 DOI: 10.1021/Acs.Jnatprod.7B00368 |
0.427 |
|
| 2017 |
Shiina I, Umezaki Y, Murata T, Suzuki K, Tonoi T. Asymmetric Total Synthesis of (+)-Coprophilin Synthesis. 50: 1301-1306. DOI: 10.1055/S-0036-1591866 |
0.473 |
|
| 2017 |
Yamada A, Nakata K, Shiina I. Acylative kinetic resolution of racemic aromatic β-hydroxy esters catalyzed by chiral nucleophilic N -(1-arylethyl)benzoguanidines Tetrahedron: Asymmetry. 28: 516-521. DOI: 10.1016/J.Tetasy.2017.03.005 |
0.369 |
|
| 2016 |
Tonoi T, Kawahara R, Inohana T, Shiina I. Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifungal activity. The Journal of Antibiotics. PMID 26814670 DOI: 10.1038/Ja.2015.146 |
0.444 |
|
| 2015 |
Tokumaru E, Tengeiji A, Nakahara T, Shiina I. Nonenzymatic, enantioconvergent dynamic kinetic resolution (DKR) of racemic 2-(1H-pyrrol-1-yl)alkanoic acids as α-amino acid equivalents Chemistry Letters. 44: 1768-1770. DOI: 10.1246/Cl.150826 |
0.37 |
|
| 2014 |
Tonoi T, Mameda K, Fujishiro M, Yoshinaga Y, Shiina I. Total synthesis of the proposed structure of astakolactin. Beilstein Journal of Organic Chemistry. 10: 2421-7. PMID 25383112 DOI: 10.3762/Bjoc.10.252 |
0.403 |
|
| 2014 |
Shiina I. Asymmetric Mukaiyama aldol reactions using chiral diamine-coordinated Sn(II) triflate: development and application to natural product synthesis. Chemical Record (New York, N.Y.). 14: 144-83. PMID 24734309 DOI: 10.1002/Tcr.201300022 |
0.464 |
|
| 2014 |
Shiina I, Nakata K. Development of kinetic resolution of racemic alcohols and carboxylic acids accompanied with dehydration condensation Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 72: 919-928. DOI: 10.5059/Yukigoseikyokaishi.72.919 |
0.346 |
|
| 2014 |
Shiina I. An adventurous synthetic journey with MNBA from its reaction chemistry to the total synthesis of natural products Bulletin of the Chemical Society of Japan. 87: 196-233. DOI: 10.1246/Bcsj.20130216 |
0.477 |
|
| 2013 |
Shiina I, Ono K, Nakahara T. Kinetic resolution of racemic α-hydroxyphosphonates by asymmetric esterification using achiral carboxylic acids with pivalic anhydride and a chiral acyl-transfer catalyst. Chemical Communications (Cambridge, England). 49: 10700-2. PMID 24100408 DOI: 10.1039/C3Cc44293D |
0.412 |
|
| 2013 |
Nakata K, Gotoh K, Ono K, Futami K, Shiina I. Kinetic resolution of racemic 2-hydroxy-γ-butyrolactones by asymmetric esterification using diphenylacetic acid with pivalic anhydride and a chiral acyl-transfer catalyst. Organic Letters. 15: 1170-3. PMID 23461674 DOI: 10.1021/Ol303453J |
0.462 |
|
| 2013 |
Shiina I, Umezaki Y, Ohashi Y, Yamazaki Y, Dan S, Yamori T. Total synthesis of AMF-26, an antitumor agent for inhibition of the Golgi system, targeting ADP-ribosylation factor 1. Journal of Medicinal Chemistry. 56: 150-9. PMID 23214926 DOI: 10.1021/Jm301695C |
0.406 |
|
| 2012 |
Tengeiji A, Shiina I. A new method for production of chiral 2-aryl-2-fluoropropanoic acids using an effective kinetic resolution of racemic 2-aryl-2-fluoropropanoic acids. Molecules (Basel, Switzerland). 17: 7356-78. PMID 22699569 DOI: 10.3390/Molecules17067356 |
0.489 |
|
| 2012 |
Shiina I, Umezaki Y, Kuroda N, Iizumi T, Nagai S, Katoh T. MNBA-mediated β-lactone formation: mechanistic studies and application for the asymmetric total synthesis of tetrahydrolipstatin. The Journal of Organic Chemistry. 77: 4885-901. PMID 22553899 DOI: 10.1021/Jo300139R |
0.422 |
|
| 2012 |
Tengeiji A, Nakata K, Ono K, Shiina I. A new method for production of chiral 2-aryloxypropanoic acids using effective kinetic resolution of racemic 2-aryloxycarboxylic acids Heterocycles. 86: 1227-1252. DOI: 10.3987/Com-12-S(N)79 |
0.384 |
|
| 2012 |
Shiina I, Ono K, Nakata K. Non-enzymatic dynamic kinetic resolution of racemic α-arylalkanoic acids: An advanced asymmetric synthesis of chiral nonsteroidal anti-inflammatory drugs (NSAIDs) Catalysis Science and Technology. 2: 2200-2205. DOI: 10.1039/C2Cy20329D |
0.462 |
|
| 2012 |
Shiina I, Nakata K, Ono K, Mukaiyama T. Kinetic resolution of racemic secondary benzylic alcohols by the enantioselective esterification using pyridine-3-carboxylic anhydride (3-PCA) with chiral acyl-transfer catalysts Helvetica Chimica Acta. 95: 1891-1911. DOI: 10.1002/Hlca.201200434 |
0.584 |
|
| 2011 |
Nakata K, Shiina I. (R)-(+)-N-methylbenzoguanidine ((R)-NMBG) catalyzed kinetic resolution of racemic secondary benzylic alcohols with free carboxylic acids by asymmetric esterification. Organic & Biomolecular Chemistry. 9: 7092-6. PMID 21887445 DOI: 10.1039/C1Ob05736G |
0.418 |
|
| 2011 |
Shiina I, Ono K, Nakata K. Kinetic resolution of racemic 1-heteroarylalkanols by asymmetric esterification using diphenylacetic acid with pivalic anhydride and a chiral acyl-transfer catalyst Chemistry Letters. 40: 147-149. DOI: 10.1246/Cl.2011.147 |
0.426 |
|
| 2011 |
Nakata K, Sekiguchi A, Shiina I. A convenient method for the kinetic resolution of racemic 2-hydroxyalkanoates using diphenylacetic anhydride (DPHAA) and a chiral acyl-transfer catalyst Tetrahedron Asymmetry. 22: 1610-1619. DOI: 10.1016/J.Tetasy.2011.08.018 |
0.382 |
|
| 2010 |
Shiina I, Nakata K, Ono K, Onda YS, Itagaki M. Kinetic resolution of racemic alpha-arylalkanoic acids with achiral alcohols via the asymmetric esterification using carboxylic anhydrides and acyl-transfer catalysts. Journal of the American Chemical Society. 132: 11629-41. PMID 20681552 DOI: 10.1021/Ja103490H |
0.456 |
|
| 2010 |
Shiina I, Nakata K, Ono K, Sugimoto M, Sekiguchi A. Kinetic resolution of the racemic 2-hydroxyalkanoates using the enantioselective mixed-anhydride method with pivalic anhydride and a chiral acyl-transfer catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 167-72. PMID 19904780 DOI: 10.1002/Chem.200902257 |
0.418 |
|
| 2010 |
Nakata K, Ono K, Shiina I. Kinetic resolution of the racemic 1-(aryloxazol-2-YL)carbinols with achiral carboxylic acids by asymmetric esterification: A new method for the preparation of chiral 1,2-amino alcohols Heterocycles. 82: 1171-1180. DOI: 10.3987/Com-10-S(E)120 |
0.423 |
|
| 2010 |
Nakata K, Shiina I. An effective kinetic resolution of racemic secondary benzylic alcohols using 3-pyridinecarboxylic anhydride and a chiral acyl-transfer catalyst in the absence of tertiary amine Heterocycles. 80: 169-175. DOI: 10.3987/Com-09-S(S)43 |
0.45 |
|
| 2010 |
Nakata K, Sano Y, Shiina I. Synthesis of lasofoxifene, nafoxidine and their positional isomers via the novel three-component coupling reaction Molecules. 15: 6773-6794. DOI: 10.3390/Molecules15106773 |
0.457 |
|
| 2010 |
Nakata K, Onda YS, Ono K, Shiina I. An effective kinetic resolution of racemic α-arylpropanoic acids, α-arylbutanoic acids, and β-substituted-α-arylpropanoic acids with bis(9-phenanthryl)methanol as a new achiral nucleophile in the asymmetric esterification using carboxylic anhydrides and the acyl-transfer catalyst Tetrahedron Letters. 51: 5666-5669. DOI: 10.1016/J.Tetlet.2010.08.008 |
0.45 |
|
| 2010 |
Mukaiyama T, Kagayama A, Igarashi K, Shiina I. ChemInform Abstract: Diastereoselective Aldol Reaction of α-Bromo Ketones with Aliphatic Aldehydes by Using Titanium(II) Chloride and Copper. Cheminform. 31: no-no. DOI: 10.1002/chin.200016028 |
0.47 |
|
| 2010 |
SAITOH K, SHIINA I, MUKAIYAMA T. ChemInform Abstract: O,O′-Di(2-pyridyl) Thiocarbonate as an Efficient Reagent for the Preparation of Carboxylic Esters from Highly Hindered Alcohols. Cheminform. 29: no-no. DOI: 10.1002/chin.199848056 |
0.401 |
|
| 2010 |
SHIINA I, SAITOH K, FRECHARD-ORTUNO I, MUKAIYAMA T. ChemInform Abstract: Total Asymmetric Synthesis of Taxol by Dehydration Condensation Between 7-TES Baccatin III and Protected N-Benzoylphenylisoserines Prepared by Enantioselective Aldol Reaction. Cheminform. 29: no-no. DOI: 10.1002/chin.199822130 |
0.511 |
|
| 2010 |
MUKAIYAMA T, IZUMI J, SHIINA I. ChemInform Abstract: New and Efficient Method for the Preparation of Medium-Sized Lactones from the Corresponding ω-Hydroxycarboxylic Acids. Cheminform. 28: no-no. DOI: 10.1002/chin.199733214 |
0.431 |
|
| 2010 |
SHIINA I, IWADARE H, SAITOH M, OHKAWA N, NISHIMURA T, MUKAIYAMA T. ChemInform Abstract: An Asymmetric Synthesis of the Fully Functionalized AB Ring System of 12-Demethyltaxol via Successive Stereoselective Allylation and Intramolecular Aldol Reactions. Cheminform. 27: no-no. DOI: 10.1002/chin.199605210 |
0.376 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, KIMURA K, AKIYAMA Y, IWADARE H. ChemInform Abstract: Synthesis of AB Ring Model System of Taxol via Allylation of 8- Membered Ring Compound and Intramolecular Aldol Condensation. Cheminform. 26: no-no. DOI: 10.1002/chin.199533213 |
0.418 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, SAKATA K, EMURA T, SETO K, SAITOH M. ChemInform Abstract: A Novel Approach to the Synthesis of Taxol. A Synthesis of Optically Active 3,7-Dibenzyloxy-4,8-di-t-butyl-dimethylsiloxy-5,5-dimethyl-6-p- methoxybenzyloxy-2-octanone by Way of Stereoselective Aldol Reactions. Cheminform. 26: no-no. DOI: 10.1002/chin.199533211 |
0.324 |
|
| 2010 |
IZUMI J, SHIINA I, MUKAIYAMA T. ChemInform Abstract: An Efficient Esterification Reaction Between Equimolar Amounts of Free Carboxylic Acids and Alcohols by the Combined Use of Octamethylcyclotetrasiloxane and a Catalytic Amount of Titanium(IV) Chloride Tris(trifluoromethanesulfonate). Cheminform. 26: no-no. DOI: 10.1002/chin.199529090 |
0.33 |
|
| 2010 |
SHIINA I, MIYASHITA M, NAGAI M, MUKAIYAMA T. ChemInform Abstract: An Effective Method for Formylation of Weakly Nucleophilic Anilines and Indole. Cheminform. 26: no-no. DOI: 10.1002/chin.199528073 |
0.399 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, UCHIRO H, KOBAYASHI S. ChemInform Abstract: Diastereo- and Enantioselective Synthesis of syn- and anti-1,2-Diol Units by Asymmetric Aldol Reactions. Cheminform. 25: no-no. DOI: 10.1002/chin.199444059 |
0.377 |
|
| 2010 |
MUKAIYAMA T, IZUMI J, MIYASHITA M, SHIINA I. ChemInform Abstract: Facile Synthesis of Lactones from Silyl ω-Siloxycarboxylates Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amounts of Active Lewis Acid. Cheminform. 25: no-no. DOI: 10.1002/chin.199415217 |
0.338 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, IZUMI J, KOBAYASHI S. ChemInform Abstract: Enantioselective Synthesis of the α-Hydroxy-α-methyl-β-hydroxy Units via Asymmetric Aldol Reaction. Cheminform. 24: no-no. DOI: 10.1002/chin.199350074 |
0.475 |
|
| 2010 |
SHIINA I, MUKAIYAMA T. ChemInform Abstract: The Esterification Reaction Between Silyl Derivatives of Carboxylic Acids and Alcohols by the Promotion of a Catalytic Amount of Lewis Acid. Cheminform. 24: no-no. DOI: 10.1002/chin.199342115 |
0.336 |
|
| 2010 |
MIYASHITA M, SHIINA I, MIYOSHI S, MUKAIYAMA T. ChemInform Abstract: A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid. Cheminform. 24: no-no. DOI: 10.1002/chin.199339136 |
0.365 |
|
| 2010 |
KOBAYASHI S, UCHIRO H, SHIINA I, MUKAIYAMA T. ChemInform Abstract: Catalytic Asymmetric Aldol-Type Reaction Using a Chiral Tin(II) Lewis Acid. Cheminform. 24: no-no. DOI: 10.1002/chin.199325059 |
0.358 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, KOBAYASHI S. ChemInform Abstract: Highly Enantioselective Synthesis of syn-α,β-Dihydroxy Thioesters by the Asymmetric Aldol Reaction Using a Chiral Tin(II) Lewis Acid. Cheminform. 23: no-no. DOI: 10.1002/chin.199247055 |
0.41 |
|
| 2010 |
MUKAIYAMA T, SHIINA I, KOBAYASHI S. ChemInform Abstract: A Convenient and Versatile Route for the Stereoselective Synthesis of Monosaccharides via Key Chiral Synthons Prepared from Achiral Sources. Cheminform. 23: no-no. DOI: 10.1002/chin.199206273 |
0.469 |
|
| 2010 |
MUKAIYAMA T, UCHIRO H, SHIINA I, KOBAYASHI S. ChemInform Abstract: Facile Synthesis of Optically Active anti-α,β-Dihydroxy Ester Derivatives. Cheminform. 22: no-no. DOI: 10.1002/chin.199151141 |
0.435 |
|
| 2009 |
Shiina I, Katoh T, Nagai S, Hashizume M. Evaluation of the efficiency of the macrolactonization using MNBA in the synthesis of erythromycin A aglycon. Chemical Record (New York, N.Y.). 9: 305-20. PMID 20041452 DOI: 10.1002/Tcr.200900017 |
0.496 |
|
| 2009 |
Shiina I, Fukui H. Chemistry and structural determination of botcinolides, botcinins, and botcinic acids. Chemical Communications (Cambridge, England). 385-400. PMID 19137164 DOI: 10.1039/B814375G |
0.369 |
|
| 2009 |
Fukui H, Shiina I. Total synthesis of botcinolides and botcinins; Determination of the structure of natural products isolated from botrytis cinerea Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 67: 628-642. DOI: 10.5059/Yukigoseikyokaishi.67.628 |
0.363 |
|
| 2009 |
Shiina I, Nakata K, Sugimoto M, Onda YS, Iizumi T, Ono K. 2,2-disubstituted propionic anhydrides: Effective coupling reagents for the kinetic resolution of secondary benzylic alcohols using BTM Heterocycles. 77: 801-810. DOI: 10.3987/Com-08-S(F)75 |
0.426 |
|
| 2009 |
Fukui H, Tsuji K, Umezaki Y, Shiina I. Total synthesis and the confirmation of the revised structures of botcinins A and B Heterocycles. 79: 403-410. DOI: 10.3987/Com-08-S(D)52 |
0.328 |
|
| 2009 |
Shiina I, Iizumi T, Yamai YS, Kawakita YI, Yokoyama K, Yamada YK. Erratum: Enantioselective aldol reaction of tetrasubstituted ketene silyl acetals with achiral aldehydes for the construction of asymmetric tertiary alcohols: An application for the divergent total syntheses of buergerinins F and G (Synthesis 2009 (2915)) Synthesis. DOI: 10.1055/S-0029-1216966 |
0.428 |
|
| 2009 |
Shiina I, Iizumi T, Yamai YS, Kawakita YI, Yokoyama K, Yamada YK. Enantioselective aldol reaction of tetrasubstituted ketene silyl acetals with achiral aldehydes for the construction of asymmetric tertiary alcohols: An application for the divergent total syntheses of buergerinins F and G Synthesis. 2915-2926. DOI: 10.1055/S-0029-1216922 |
0.474 |
|
| 2008 |
Fukui H, Shiina I. Asymmetric total synthesis of botcinins C, D, and F. Organic Letters. 10: 3153-6. PMID 18549237 DOI: 10.1021/Ol801066Y |
0.397 |
|
| 2008 |
Shiina I, Ushiyama H, Yamada YK, Kawakita Y, Nakata K. 4-(Dimethylamino)pyridine N-oxide (DMAPO): an effective nucleophilic catalyst in the peptide coupling reaction with 2-methyl-6-nitrobenzoic anhydride. Chemistry, An Asian Journal. 3: 454-61. PMID 18219641 DOI: 10.1002/Asia.200700305 |
0.44 |
|
| 2008 |
Shiina I, Sasaki A, Kikuchi T, Fukui H. Total synthesis of 2-hydroxytetracosanolide and 2-hydroxy-24-oxooctacosanolide by using an effective lactonization. Chemistry, An Asian Journal. 3: 462-72. PMID 18203212 DOI: 10.1002/Asia.200700304 |
0.412 |
|
| 2008 |
Shiina I, Miyao R. 2,6-Dimethyl-4-nitrobenzoic anhydride (DMNBA): An effective coupling reagent for the synthesis of carboxylic esters and lactones Heterocycles. 76: 1313-1328. DOI: 10.3987/Com-08-S(N)96 |
0.493 |
|
| 2008 |
Fukui H, Hitomi S, Suzuki Rs, Ikeda T, Umezaki Y, Tsuji K, Shiina I. Asymmetric total synthesis of botcinic acid and its derivatives: synthetic revision of the structure of botcinolides Tetrahedron Letters. 49: 6514-6517. DOI: 10.1016/J.Tetlet.2008.08.108 |
0.382 |
|
| 2008 |
Shiina I, Nakata K, Onda YS. Kinetic resolution of racemic carboxylic acids using achiral alcohols by the promotion of benzoic anhydrides and tetramisole derivatives: Production of chiral nonsteroidal anti-inflammatory drugs and their esters European Journal of Organic Chemistry. 5887-5890. DOI: 10.1002/Ejoc.200800942 |
0.477 |
|
| 2007 |
Shiina I, Fukui H, Sasaki A. Synthesis of lactones using substituted benzoic anhydride as a coupling reagent. Nature Protocols. 2: 2312-7. PMID 17947971 DOI: 10.1038/Nprot.2007.316 |
0.483 |
|
| 2007 |
Shiina I, Sano Y, Nakata K, Suzuki M, Yokoyama T, Sasaki A, Orikasa T, Miyamoto T, Ikekita M, Nagahara Y, Hasome Y. An expeditious synthesis of tamoxifen, a representative SERM (selective estrogen receptor modulator), via the three-component coupling reaction among aromatic aldehyde, cinnamyltrimethylsilane, and beta-chlorophenetole. Bioorganic & Medicinal Chemistry. 15: 7599-617. PMID 17904372 DOI: 10.1016/J.Bmc.2007.09.008 |
0.467 |
|
| 2007 |
Shiina I, Sano Y, Nakata K, Kikuchi T, Sasaki A, Ikekita M, Hasome Y. Synthesis of the new pseudo-symmetrical tamoxifen derivatives and their anti-tumor activity. Bioorganic & Medicinal Chemistry Letters. 17: 2421-4. PMID 17346960 DOI: 10.1016/J.Bmcl.2007.02.037 |
0.363 |
|
| 2007 |
Shiina I. Total synthesis of natural 8- and 9-membered lactones: recent advancements in medium-sized ring formation. Chemical Reviews. 107: 239-73. PMID 17212476 DOI: 10.1021/Cr050045O |
0.353 |
|
| 2007 |
Sano Y, Nakata K, Otoyama T, Umeda S, Shiina I. An expeditious synthesis of lasofoxifene and nafoxidine via the novel three-component coupling reaction Chemistry Letters. 36: 40-41. DOI: 10.1246/Cl.2007.40 |
0.427 |
|
| 2007 |
Shiina I, Nakata K. The first asymmetric esterification of free carboxylic acids with racemic alcohols using benzoic anhydrides and tetramisole derivatives: an application to the kinetic resolution of secondary benzylic alcohols Tetrahedron Letters. 48: 8314-8317. DOI: 10.1016/J.Tetlet.2007.09.135 |
0.447 |
|
| 2006 |
Shiina I, Takasuna YJ, Suzuki RS, Oshiumi H, Komiyama Y, Hitomi S, Fukui H. Stereoselective total synthesis of the proposed structure of 2-epibotcinolide. Organic Letters. 8: 5279-82. PMID 17078697 DOI: 10.1021/Ol062058+ |
0.484 |
|
| 2006 |
Shiina I, Kikuchi T, Sasaki A. The first total synthesis of (-) and (+)-2-hydroxy-24-oxooctacosanolide using an effective lactonization. Organic Letters. 8: 4955-8. PMID 17020345 DOI: 10.1021/Ol062011O |
0.428 |
|
| 2006 |
Sano Y, Shiina I. Short-step synthesis of droloxifene via the three-component coupling reaction among aromatic aldehyde, cinnamyltrimethylsilane, and β-chlorophenetole Tetrahedron Letters. 47: 1631-1635. DOI: 10.1016/J.Tetlet.2005.12.117 |
0.434 |
|
| 2006 |
Shiina I, Hashizume M. Synthesis of (9E)-isoambrettolide, a macrocyclic musk compound, using the effective lactonization promoted by symmetric benzoic anhydrides with basic catalysts Tetrahedron. 62: 7934-7939. DOI: 10.1016/J.Tet.2006.04.077 |
0.446 |
|
| 2005 |
Shoji M, Uno T, Kakeya H, Onose R, Shiina I, Osada H, Hayashi Y. Enantio- and diastereoselective total synthesis of EI-1941-1, -2, and -3, inhibitors of interleukin-1beta converting enzyme, and biological properties of their derivatives. The Journal of Organic Chemistry. 70: 9905-15. PMID 16292821 DOI: 10.1021/Jo0516436 |
0.368 |
|
| 2005 |
Shiina I, Yamai YS, Shimazaki T. Enantioselective synthesis of the optically active alpha-methylene-beta-hydroxy esters, equivalent compounds to Morita-Baylis-Hillman adducts, using successive asymmetric aldol reaction and oxidative deselenization. The Journal of Organic Chemistry. 70: 8103-6. PMID 16277334 DOI: 10.1021/Jo051276Y |
0.445 |
|
| 2005 |
Shiina I, Hashizume M, Yamai YS, Oshiumi H, Shimazaki T, Takasuna YJ, Ibuka R. Enantioselective total synthesis of octalactin a using asymmetric aldol reactions and a rapid lactonization to form a medium-sized ring. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 6601-8. PMID 16118824 DOI: 10.1002/Chem.200500417 |
0.486 |
|
| 2005 |
Shiina I, Kawakita Y, Ibuka R, Yokoyama K, Yamai YS. Total synthesis of buergerinin F via effective construction of the asymmetric quaternary carbons using an enantioselective aldol reaction. Chemical Communications (Cambridge, England). 4062-4. PMID 16091800 DOI: 10.1039/B507401K |
0.445 |
|
| 2005 |
Shiina I. An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones - Powerful and convenient mixed anhydride methods promoted by Lewis acids or basic catalysts Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 63: 2-17. DOI: 10.5059/Yukigoseikyokaishi.63.2 |
0.496 |
|
| 2005 |
Hayashi Y, Urushima T, Shoji M, Uchimaru T, Shiina I. The direct, enantioselective, one-pot, three-component, cross-Mannich reaction of aldehydes: The reason for the higher reactivity of aldimine versus aldehyde in proline-mediated Mannich and aldol reactions Advanced Synthesis and Catalysis. 347: 1595-1604. DOI: 10.1002/Adsc.200505190 |
0.421 |
|
| 2004 |
Shiina I, Kubota M, Oshiumi H, Hashizume M. An effective use of benzoic anhydride and its derivatives for the synthesis of carboxylic esters and lactones: a powerful and convenient mixed anhydride method promoted by basic catalysts. The Journal of Organic Chemistry. 69: 1822-30. PMID 15058924 DOI: 10.1021/Jo030367X |
0.521 |
|
| 2004 |
Shoji M, Imai H, Shiina I, Kakeya H, Osada H, Hayashi Y. Different reaction modes for the oxidative dimerization of epoxyquinols and epoxyquinones. Importance of intermolecular hydrogen-bonding. The Journal of Organic Chemistry. 69: 1548-56. PMID 14987010 DOI: 10.1021/Jo0355303 |
0.359 |
|
| 2004 |
Shiina I, Suzuki M, Yokoyama K. Short-step synthesis of tamoxifen and its derivatives via the three-component coupling reaction and migration of the double bond Tetrahedron Letters. 45: 965-967. DOI: 10.1016/J.Tetlet.2003.11.119 |
0.446 |
|
| 2004 |
Shiina I, Oshiumi H, Hashizume M, Yamai YS, Ibuka R. Asymmetric total synthesis of octalactin B using a new and rapid lactonization Tetrahedron Letters. 45: 543-547. DOI: 10.1016/J.Tetlet.2003.10.213 |
0.49 |
|
| 2004 |
Shiina I, Kawakita YI. The effective use of substituted benzoic anhydrides for the synthesis of carboxamides Tetrahedron. 60: 4729-4733. DOI: 10.1016/J.Tet.2004.03.066 |
0.461 |
|
| 2004 |
Shiina I. An effective method for the synthesis of carboxylic esters and lactones using substituted benzoic anhydrides with Lewis acid catalysts Tetrahedron. 60: 1587-1599. DOI: 10.1016/J.Tet.2003.12.013 |
0.498 |
|
| 2003 |
Shoji M, Kishida S, Kodera Y, Shiina I, Kakeya H, Osada H, Hayashi Y. Reaction modes of oxidative dimerization of epoxycyclohexenols Tetrahedron Letters. 44: 7205-7207. DOI: 10.1016/S0040-4039(03)01781-7 |
0.307 |
|
| 2003 |
Shiina I, Kawakita YI. A new method for the synthesis of carboxamides and peptides using 1,1′-carbonyldioxydi[2(1H)-pyridone] (CDOP) in the absence of basic promoters Tetrahedron Letters. 44: 1951-1955. DOI: 10.1016/S0040-4039(03)00063-7 |
0.417 |
|
| 2002 |
Shiina I, Ibuka R, Kubota M. A new condensation reaction for the synthesis of carboxylic esters from nearly equimolar amounts of carboxylic acids and alcohols using 2-methyl-6-nitrobenzoic anhydride Chemistry Letters. 286-287. DOI: 10.1246/Cl.2002.286 |
0.463 |
|
| 2002 |
Shiina I, Konishi K, Kuramoto Ys. Enantioselective alkylation of aldehydes with diethylzinc using a new catalyst system, ((R)-thiolan-2-yl)diphenylmethanol and metal alkoxides Chemistry Letters. 164-165. DOI: 10.1246/Cl.2002.164 |
0.346 |
|
| 2002 |
Shiina I, Kubota M, Ibuka R. A novel and efficient macrolactonization of ω-hydroxycarboxylic acids using 2-methyl-6-nitrobenzoic anhydride (MNBA) Tetrahedron Letters. 43: 7535-7539. DOI: 10.1016/S0040-4039(02)01819-1 |
0.498 |
|
| 2002 |
Shiina I, Suzuki M. The catalytic Friedel-Crafts alkylation reaction of aromatic compounds with benzyl or allyl silyl ethers using Cl2Si(OTf)2 or Hf(OTf)4 Tetrahedron Letters. 43: 6391-6394. DOI: 10.1016/S0040-4039(02)01376-X |
0.484 |
|
| 2002 |
Shiina I, Suzuki M, Yokoyama K. A convenient method for the synthesis of 4,4-diarylbut-1-enes via the successive allylation of aromatic aldehydes and the Friedel-Crafts alkylation reaction of aromatic nucleophiles with the intermediary benzyl silyl ethers using HfCl4 or Cl2Si(OTf)2 Tetrahedron Letters. 43: 6395-6398. DOI: 10.1016/S0040-4039(02)01374-6 |
0.484 |
|
| 2002 |
Shiina I, Nagasue H. [1,3] Sigmatropic rearrangement of ketene silyl acetals derived from benzyl α-substituted propanoates Tetrahedron Letters. 43: 5837-5840. DOI: 10.1016/S0040-4039(02)01168-1 |
0.471 |
|
| 2001 |
Arai H, Shiina I, Mukaiyama T. A convenient method for the preparation of unsymmetrical bis-aldols by way of sequential two aldol reactions Chemistry Letters. 118-119. DOI: 10.1246/Cl.2001.118 |
0.475 |
|
| 2001 |
Arai H, Shiina I, Mukaiyama T. A Convenient Method for the Preparation of Unsymmetrical Bis-Aldols by Way of Sequential Two Aldol Reactions Chemistry Letters. 30: 118-119. DOI: 10.1246/cl.2001.118 |
0.472 |
|
| 2001 |
Shiina I, Shibata J, Ibuka R, Imai Y, Mukaiyama T. An effective method for the preparation of chiral polyoxy 8-membered ring enone corresponding to the B ring of taxol Bulletin of the Chemical Society of Japan. 74: 113-122. DOI: 10.1246/Bcsj.74.113 |
0.337 |
|
| 2001 |
Shiina I, Ibuka R. Enantioselective synthesis of β-hydroxy-α-methyl-α-methylthio esters as precursors of anti-vic-hydroxymethyl units Tetrahedron Letters. 42: 6303-6306. DOI: 10.1016/S0040-4039(01)01238-2 |
0.467 |
|
| 2001 |
Shiina I, Shibata J, Ibuka R, Imai Y, Mukaiyama T. ChemInform Abstract: An Effective Method for the Preparation of Chiral Polyoxy 8-Membered Ring Enone Corresponding to the B Ring of Taxol. Cheminform. 32: no-no. DOI: 10.1002/chin.200117191 |
0.422 |
|
| 2001 |
Shiina I, Suenaga Y, Nakano M, Mukaiyama T. ChemInform Abstract: A Convenient Method for the Preparations of Carboxamides and Peptides by Using Di(2-pyridyl) Carbonate and O,O′-Di(2-pyridyl) Thiocarbonate as Dehydrating Reagents. Cheminform. 32: no-no. DOI: 10.1002/chin.200115070 |
0.332 |
|
| 2001 |
Shiina I, Imai Y, Suzuki M, Yanagisawa M, Mukaiyama T. ChemInform Abstract: Direct and Selective Syntheses of α,α-Dichloroethyl Ketones or Their Ethyl Trimethylsilyl Mixed Acetals by the Reactions of Methoxymethyl or Ethyl Carboxylates with 1,1-Dichloroethyllithium in the Presence of Chlorotrimethylsilane. Cheminform. 32: no-no. DOI: 10.1002/chin.200103068 |
0.473 |
|
| 2000 |
Shiina I, Fujisawa H, Ishii T, Fukuda Y. Stereoselective total synthesis of cephalosporolide D Heterocycles. 52: 1105-1123. DOI: 10.3987/Com-99-S85 |
0.334 |
|
| 2000 |
Mukaiyama T, Arai H, Shiina I. A new method for the synthesis of unsymmetrical bis-aldols by the samarium(II) iodide-mediated aldol reaction of aldehydes with aryl or alkyl oxiranyl ketones Chemistry Letters. 580-581. DOI: 10.1246/Cl.2000.580 |
0.49 |
|
| 2000 |
Shiina I, Imai Y, Kagayama A, Mukaiyama T. A direct and selective syntheses of α,α-dichloro-and α-chloro-ethyl ketones by the reaction of alkyl carboxylates with 1,1-dichloroethyllithium Chemistry Letters. 190-191. DOI: 10.1246/Cl.2000.190 |
0.404 |
|
| 2000 |
Shiina I, Imai Y, Suzuki M, Yanagisawa M, Mukaiyama T. Direct and selective syntheses of α,α-dichloroethyl ketones or their ethyl trimethylsilyl mixed acetals by the reactions of methoxymethyl or ethyl carboxylates with 1,1-dichloroethyllithium in the presence of chlorotrimethylsilane Chemistry Letters. 1062-1063. DOI: 10.1246/Cl.2000.1062 |
0.459 |
|
| 2000 |
Shiina I, Suenaga Y, Nakano M, Mukaiyama T. A convenient method for the preparations of carboxamides and peptides by using di(2-pyridyl) carbonate and O,O′-di(2-pyridyl) thiocarbonate as dehydrating reagents Bulletin of the Chemical Society of Japan. 73: 2811-2818. DOI: 10.1246/Bcsj.73.2811 |
0.422 |
|
| 2000 |
Kagayama A, Igarashi K, Shiina I, Mukaiyama T. Diastereoselective aldol and reformatsky reactions of α-halo carbonyl compounds and aldehydes mediated by Titanium(II) Chloride Bulletin of the Chemical Society of Japan. 73: 2579-2585. DOI: 10.1246/Bcsj.73.2579 |
0.467 |
|
| 2000 |
Shiina I, Saitoh K, Nakano M, Suenaga Y, Mukaiyama T. A facile synthesis of carboxamides by dehydration condensation between free carboxylic acids and amines using O,O′-DI(2-pyridyl) thiocarbonate as a coupling reagent Collection of Czechoslovak Chemical Communications. 65: 621-630. DOI: 10.1135/Cccc20000621 |
0.42 |
|
| 2000 |
Mukaiyama T, Arai H, Shiina I. ChemInform Abstract: A New Method for the Synthesis of Unsymmetrical Bis-Aldols by the Samarium(II) Iodide-Mediated Aldol Reaction of Aldehydes with Aryl or Alkyl Oxiranyl Ketones. Cheminform. 31: no-no. DOI: 10.1002/chin.200039078 |
0.522 |
|
| 2000 |
Shiina I, Saitoh K, Nakano M, Suenaga Y, Mukaiyama T. ChemInform Abstract: A Facile Synthesis of Carboxamides by Dehydration Condensation Between Free Carboxylic Acids and Amines Using O,O′-Di(2-pyridyl) Thiocarbonate as a Coupling Reagent. Cheminform. 31: no-no. DOI: 10.1002/chin.200038073 |
0.458 |
|
| 1999 |
Mukaiyama T, Shibata J, Shimamura T, Shiina I. Diethylaluminum ethoxide mediated crossed aldol reaction of enol esters with carbonyl compounds Chemistry Letters. 951-952. DOI: 10.1246/Cl.1999.951 |
0.456 |
|
| 1999 |
Iwadare H, Sakoh H, Arai H, Shiina I, Mukaiyama T. Synthesis of 18-demethyltaxoid via stereoselective allylation and intramolecular aldol condensation reactions Chemistry Letters. 817-818. DOI: 10.1246/Cl.1999.817 |
0.426 |
|
| 1999 |
Shibata J, Shiina I, Mukaiyama T. Diethylaluminum ethoxide mediated stereoselective Diels-Alder reaction of α,β-unsaturated ketones and acetoxy-1,3-butadienes as diene components Chemistry Letters. 313-314. DOI: 10.1246/Cl.1999.313 |
0.482 |
|
| 1999 |
Shibata J, Shiina I, Mukaiyama T. Diethylaluminum Ethoxide Mediated Stereoselective Diels-Alder Reaction ofα,β-unsaturated Ketones and Acetoxy-1,3-butadienes as Diene Components Chemistry Letters. 28: 313-314. DOI: 10.1246/cl.1999.313 |
0.454 |
|
| 1999 |
Mukaiyama T, Kagayama A, Igarashi K, Shiina I. Diastereoselective aldol reaction of α-bromo ketones with aliphatic aldehydes by using titanium(II) chloride and copper Chemistry Letters. 1157-1158. DOI: 10.1246/Cl.1999.1157 |
0.458 |
|
| 1999 |
Shiina I, Shibata J, Imai Y, Ibuka R, Fujisawa H, Hachiya I, Mukaiyama T. An effective method for the preparation of optically active polyoxy 8-membered ring enone corresponding to the B ring of taxol Chemistry Letters. 1145-1146. DOI: 10.1246/Cl.1999.1145 |
0.479 |
|
| 1999 |
Mukaiyama T, Shiina I, Iwadare H, Saitoh M, Nishimura T, Ohkawa N, Sakoh H, Nishimura K, Tani Y, Hasegawa M, Yamada K, Saitoh K. Asymmetric Total Synthesis of TaxolR Chemistry: a European Journal. 5: 121-161. DOI: 10.1002/(Sici)1521-3765(19990104)5:1<121::Aid-Chem121>3.3.Co;2-F |
0.528 |
|
| 1999 |
Mukaiyama T, Shiina I, Iwadare H, Saitoh M, Nishimura T, Ohkawa N, Sakoh H, Nishimura K, Tani Y, Hasegawa M, Yamada K, Saitoh K. Asymmetric Total Synthesis of Taxol\R Chemistry: a European Journal. 5: 121-161. DOI: 10.1002/(Sici)1521-3765(19990104)5:1<121::Aid-Chem121>3.0.Co;2-O |
0.547 |
|
| 1999 |
Mukaiyama T, Shiina I, Iwadare H, Saitoh M, Nishimura T, Ohkawa N, Sakoh H, Nishimura K, Tani YI, Hasegawa M, Yamada K, Saitoh K. Asymmetric total synthesis of Taxol Chemistry - a European Journal. 5: 121-161. |
0.319 |
|
| 1998 |
Shiina I, Fukuda Y, Ishii T, Fujisawa H, Mukaiyama T. Determination of Relative and Absolute Stereochemistry of Cephalosporolide D and Its Enantioselective Total Synthesis Chemistry Letters. 27: 831-832. DOI: 10.1246/Cl.1998.831 |
0.448 |
|
| 1998 |
Saitoh K, Shiina I, Mukaiyama T. O,O′-di(2-pyridyl) thiocarbonate as an efficient reagent for the preparation of carboxylic esters from highly hindered alcohols Chemistry Letters. 679-680. DOI: 10.1246/Cl.1998.679 |
0.386 |
|
| 1998 |
Shiina I, Saitoh K, Fréchard-Ortuno I, Mukaiyama T. Total asymmetric synthesis of taxol by dehydration condensation between 7-TES baccatin III and protected N-benzoylphenylisoserines prepared by enantioselective aldol reaction Chemistry Letters. 3-4. DOI: 10.1246/Cl.1998.3 |
0.471 |
|
| 1998 |
Mukaiyama T, Kagayama A, Shiina I. Efficient method for pinacol coupling of aromatic and aliphatic ketones by using titanium(II) chloride and zinc in the presence of pivalonitrile Chemistry Letters. 1107-1108. DOI: 10.1246/Cl.1998.1107 |
0.418 |
|
| 1998 |
Shiina I, Iwadare H, Sakoh H, Hasegawa M, Tani YI, Mukaiyama T. A new method for the synthesis of baccatin III Chemistry Letters. 1-2. DOI: 10.1246/Cl.1998.1 |
0.344 |
|
| 1997 |
Shiina I, Nishimura T, Ohkawa N, Sakoh H, Nishimura K, Saitoh K, Mukaiyama T. An asymmetric synthesis of the ABC ring system of 8-demethyltaxoids from optically active 8-membered ring compound via intramolecular aldol and pinacol coupling reactions Chemistry Letters. 419-420. DOI: 10.1246/Cl.1997.419 |
0.414 |
|
| 1997 |
Mukaiyama T, Izumi J, Shiina I. New and Efficient Method for the Preparation of Medium-sized Lactones from the Correspondingω-Hydroxycarboxylic Acids Chemistry Letters. 1997: 187-188. DOI: 10.1246/Cl.1997.187 |
0.522 |
|
| 1997 |
Shiina I, Iwadare H, Sakoh H, Tani YI, Hasegawa M, Saitoh K, Mukaiyama T. Stereocontrolled synthesis of the BC ring system of Taxol Chemistry Letters. 1139-1140. DOI: 10.1246/Cl.1997.1139 |
0.425 |
|
| 1997 |
Mukaiyama T, Shiina I, Iwadare H, Sakoh H, Tani YI, Hasegawa M, Saitoh K. Asymmetric total synthesis of Taxol® Proceedings of the Japan Academy Series B: Physical and Biological Sciences. 73: 95-100. |
0.317 |
|
| 1996 |
Mukaiyama T, Shiina I, Iwadare H, Saitoh M, Nishimura K, Nishimura T, Ohkawa N, Sakoh H, Saitoh K. An asymmetric synthesis of the BC ring system of 8-epitaxoids by way of intramolecular aldol and successive stereoselective methylation reactions Chemistry Letters. 483-484. DOI: 10.1246/Cl.1996.483 |
0.439 |
|
| 1995 |
Shiina I, Miyashita M, Nagai M, Mukaiyama T. An effective method for formylation of weakly nucleophilic anilines and indole Heterocycles. 40: 141-148. DOI: 10.3987/Com-94-S40 |
0.333 |
|
| 1995 |
Shiina I, Iwadare H, Saitoh M, Ohkawa N, Nishimura T, Mukaiyama T. An Asymmetric Synthesis of the Fully Functionalized AB Ring System of 12-DemethyltaxolviaSuccessive Stereoselective Allylation and Intramolecular Aldol Reactions Chemistry Letters. 24: 781-782. DOI: 10.1246/Cl.1995.781 |
0.453 |
|
| 1995 |
Mukaiyama T, Shiina I, Kimura K, Akiyama Y, Iwadare H. Synthesis of AB Ring Model System of TaxolviaAllylation of 8-Membered Ring Compound and Intramolecular Aldol Condensation Chemistry Letters. 24: 229-230. DOI: 10.1246/Cl.1995.229 |
0.503 |
|
| 1995 |
Shiina I, Uoto K, Mori N, Kosugi T, Mukaiyama T. An Asymmetric Synthesis of Fully Functionalized B Ring System of Taxol Chemistry Letters. 24: 181-182. DOI: 10.1246/Cl.1995.181 |
0.371 |
|
| 1995 |
Mukaiyama T, Shiina I, Sakata K, Emura T, Seto K, Saitoh M. A Novel Approach to the Synthesis of Taxol. A Synthesis of Optically Active 3,7-dibenzyloxy-4,8-di-t-butyl-dimethylsiloxy-5,5-dimethyl-6-p-methoxybenzyloxy-2-octanone by Way of Stereoselective Aldol Reactions Chemistry Letters. 24: 179-180. DOI: 10.1246/Cl.1995.179 |
0.495 |
|
| 1995 |
Izumi J, Shiina I, Mukaiyama T. An Efficient Esterification Reaction between Equimolar Amounts of Free Carboxylic Acids and Alcohols by the Combined Use of Octamethylcyclotetrasiloxane and a Catalytic Amount of Titanium(IV) Chloride Tris(trifluoromethanesulfonate) Chemistry Letters. 24: 141-142. DOI: 10.1246/Cl.1995.141 |
0.435 |
|
| 1995 |
Mukaiyama T, Watanabe K, Shiina I. The Catalytic Diels-Alder Reaction Using Combined Catalyst System of Diphenyltin Sulfide or Lawesson’s Reagent and Silver Perchlorate Chemistry Letters. 24: 1-2. DOI: 10.1246/Cl.1995.1 |
0.458 |
|
| 1994 |
Shiina I, Mukaiyama T. A Novel Method for the Preparation of Macrolides from ω-Hydroxycarboxylic Acids Chemistry Letters. 23: 677-680. DOI: 10.1246/Cl.1994.677 |
0.544 |
|
| 1994 |
Shiina I, Miyoshi S, Miyashita M, Mukaiyama T. A Useful Method for the Preparation of Carboxylic Esters from Free Carboxylic Acids and Alcohols Chemistry Letters. 23: 515-518. DOI: 10.1246/Cl.1994.515 |
0.517 |
|
| 1994 |
Miyashita M, Shiina I, Mukaiyama T. An Effective Method for Acylation of Weakly Nucleophilic Anilines with Silyl Carboxylates via Mixed Anhydrides Bulletin of the Chemical Society of Japan. 67: 210-215. DOI: 10.1246/Bcsj.67.210 |
0.475 |
|
| 1994 |
Mukaiyama T, Shiina I, Uchiro H, Kobayashi S. Diastereo- and Enantioselective Synthesis ofsyn- andanti-1,2-Diol Units by Asymmetric Aldol Reactions Bulletin of the Chemical Society of Japan. 67: 1708-1716. DOI: 10.1246/Bcsj.67.1708 |
0.522 |
|
| 1993 |
Mukaiyama T, Shiina I, Izumi J, Kobayashi S. Enantioselective synthesis of the α-hydroxy-α-methyl-β-hydroxy units via asymmetric aldol reaction Heterocycles. 35: 719-724. DOI: 10.3987/Com-93-S(T)138 |
0.428 |
|
| 1993 |
Mukaiyama T, Izumi J, Miyashita M, Shiina I. Facile Synthesis of Lactones from Silyl ω-Siloxycarboxylates Usingp-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Lewis Acid Chemistry Letters. 22: 907-910. DOI: 10.1246/Cl.1993.907 |
0.547 |
|
| 1993 |
Miyashita M, Shiina I, Mukaiyama T. A Convenient Synthesis of Carboxanilides from Silyl Carboxylates and Weakly Nucleophilic Anilines Usingp-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Titanium(IV) Salt Chemistry Letters. 22: 1053-1054. DOI: 10.1246/Cl.1993.1053 |
0.57 |
|
| 1993 |
Miyashita M, Shiina I, Miyoshi S, Mukaiyama T. A New and Efficient Esterification Reaction via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid Bulletin of the Chemical Society of Japan. 66: 1516-1527. DOI: 10.1246/Bcsj.66.1516 |
0.522 |
|
| 1993 |
Kobayashi S, Uchiro H, Shiina I, Mukaiyama T. Catalytic asymmetric aldol-type reaction using a chiral tin(II) Lewis acid Tetrahedron. 49: 1761-1772. DOI: 10.1016/S0040-4020(01)80533-0 |
0.5 |
|
| 1992 |
Mukaiyama T, Shiina I, Miyashita M. An Efficient Method for the Preparation of Carboxylic Esters via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid Chemistry Letters. 21: 625-628. DOI: 10.1246/Cl.1992.625 |
0.581 |
|
| 1992 |
Kobayashi S, Shiina I, Izumi J, Mukaiyama T. An Efficient Method for the Preparation of Chiral Synthons Starting from Racemic Compounds by Way of Asymmetric Synthesis Chemistry Letters. 21: 373-376. DOI: 10.1246/Cl.1992.373 |
0.589 |
|
| 1992 |
Shiina I, Mukaiyama T. The Esterification Reaction between Silyl Derivatives of Carboxylic Acids and Alcohols by the Promotion of a Catalytic Amount of Lewis Acid Chemistry Letters. 21: 2319-2320. DOI: 10.1246/Cl.1992.2319 |
0.466 |
|
| 1992 |
Mukaiyama T, Miyashita M, Shiina I. A New and Efficient Method for the Preparation ofS-Phenyl Carbothioates via Mixed Anhydrides Using Active Titanium(IV) Salts Chemistry Letters. 21: 1747-1750. DOI: 10.1246/Cl.1992.1747 |
0.587 |
|
| 1992 |
MUKAIYAMA T, SHIINA I, MIYASHITA M. ChemInform Abstract: An Efficient Method for the Preparation of Carboxylic Esters via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid. Cheminform. 23: no-no. DOI: 10.1002/chin.199251130 |
0.346 |
|
| 1992 |
KOBAYASHI S, SHIINA I, IZUMI J, MUKAIYAMA T. ChemInform Abstract: An Efficient Method for the Preparation of Chiral Synthons Starting from Racemic Compounds by Way of Asymmetric Synthesis. Cheminform. 23: no-no. DOI: 10.1002/chin.199251059 |
0.476 |
|
| 1991 |
Mukaiyama T, Shiina I, Kobayashi S. Highly Enantioselective Synthesis of syn-α,β-Dihydroxy Thioesters by the Asymmetric Aldol Reaction Using a Chiral Tin(II) Lewis Acid Chemistry Letters. 20: 1901-1904. DOI: 10.1246/Cl.1991.1901 |
0.586 |
|
| 1991 |
Kobayashi S, Uchiro H, Fujishita Y, Shiina I, Mukaiyama T. Asymmetric Aldol Reaction between Achiral Silyl Enol Ethers and Achiral Aldehydes by Use of a Chiral Promoter System Journal of the American Chemical Society. 113: 4247-4252. DOI: 10.1021/Ja00011A030 |
0.514 |
|
| 1990 |
Mukaiyama T, Shiina I, Kobayashi S. A Convenient and Versatile Route for the Stereoselective Synthesis of Monosaccharides via Key Chiral Synthons Prepared from Achiral Sources Chemistry Letters. 19: 2201-2204. DOI: 10.1246/Cl.1990.2201 |
0.548 |
|
| 1990 |
Mukaiyama T, Kobayashi S, Uchiro H, Shiina I. Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine Coordinated Tin(II) Triflate Chemistry Letters. 19: 129-132. DOI: 10.1246/Cl.1990.129 |
0.558 |
|
| 1990 |
Mukaiyama T, Uchiro H, Shiina I, Kobayashi S. Facile Synthesis of Optically Active anti-α,β-Dihydroxy Ester Derivatives Chemistry Letters. 19: 1019-1022. DOI: 10.1246/Cl.1990.1019 |
0.461 |
|
| 1990 |
MUKAIYAMA T, KOBAYASHI S, UCHIRO H, SHIINA I. ChemInform Abstract: Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine-Coordinated Tin(II) Triflate. Cheminform. 21. DOI: 10.1002/chin.199037101 |
0.366 |
|
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