Year |
Citation |
Score |
2011 |
Teraoka F, Fuji K, Ozturk O, Yoshimura T, Kawabata T. Asymmetric Carbonyl Migrationof α-Amino Acid Derivatives via Memory of Chirality Synlett. 2011: 543-546. DOI: 10.1055/S-0030-1259324 |
0.36 |
|
2005 |
Tsubaki K, Tanima D, Nuruzzaman M, Kusumoto T, Fuji K, Kawabata T. Visual enantiomeric recognition of amino acid derivatives in protic solvents. The Journal of Organic Chemistry. 70: 4609-16. PMID 15932296 DOI: 10.1021/Jo050387U |
0.305 |
|
2004 |
Kinoshita N, Marx KH, Tanaka K, Tsubaki K, Kawabata T, Yoshikai N, Nakamura E, Fuji K. Enantioselective allylic substitution of cinnamyl esters catalyzed by iridium-chiral aryl phosphite complex: conspicuous change in the mechanistic spectrum by a countercation and solvent. The Journal of Organic Chemistry. 69: 7960-4. PMID 15527276 DOI: 10.1021/Jo048834D |
0.394 |
|
2003 |
Kawabata T, Oztürk O, Chen J, Fuji K. Chirality transfer during alkylation of chiral amides. Chemical Communications (Cambridge, England). 162-3. PMID 12611016 DOI: 10.1039/B209736B |
0.384 |
|
2003 |
Kawabata T, Stragies R, Fukaya T, Fuji K. Remote chirality transfer in nucleophilic catalysis with N-(4-pyridinyl)-L-proline derivatives Chirality. 15: 71-76. PMID 12467046 DOI: 10.1002/Chir.10166 |
0.323 |
|
2003 |
Tsubaki K, Morikawa H, Tanaka H, Fuji K. Convenient synthesis and efficient resolution of 3,3′-bis(benzyloxy)-1,1′-binaphthalene-2,2′-diol Tetrahedron-Asymmetry. 14: 1393-1396. DOI: 10.1016/S0957-4166(03)00219-2 |
0.347 |
|
2003 |
Kawabata T, Stragies R, Fukaya T, Nagaoka Y, Schedel H, Fuji K. Preparation and properties of chiral 4-pyrrolidinopyridine (PPY) analogues with dual functional side chains Tetrahedron Letters. 44: 1545-1548. DOI: 10.1016/S0040-4039(03)00021-2 |
0.334 |
|
2003 |
Kawabata T, Kawakami S, Shimada S, Fuji K. Control of the enantioselectivity of alkylation of phenylalanine derivatives by regulation of the aggregate structure of chiral enolate intermediates Tetrahedron. 59: 965-974. DOI: 10.1016/S0040-4020(02)01626-5 |
0.38 |
|
2002 |
Tsubaki K, Mukoyoshi K, Morikawa H, Kinoshita T, Fuji K. Enantiomeric recognition of amino acids using a chiral spiropyran derivative. Chirality. 14: 713-5. PMID 12237830 DOI: 10.1002/Chir.10111 |
0.352 |
|
2002 |
Yamazaki J, Bedekar AV, Watanabe T, Tanaka K, Watanabe J, Fuji K. Asymmetric construction of novel bicyclo[4.4.0] and [4.3.0]ring systems via intramolecular Horner–Wadsworth–Emmons reactions Tetrahedron-Asymmetry. 13: 729-734. DOI: 10.1016/S0957-4166(02)00177-5 |
0.392 |
|
2002 |
Kawabata T, Kawakami S, Fuji K. Enantioselective α-allylation of a phenylalanine derivative under the control of aggregation of a chiral nonracemic enolate Tetrahedron Letters. 43: 1465-1467. DOI: 10.1016/S0040-4039(02)00034-5 |
0.363 |
|
2002 |
Tsubaki K, Tanaka H, Furuta T, Tanaka K, Kinoshita T, Fuji K. Use of meso-ternaphthalene derivatives: linear recognition of the α,ω-diamines by homoditopic receptors Tetrahedron. 58: 5611-5617. DOI: 10.1016/S0040-4020(02)00547-1 |
0.303 |
|
2002 |
Tsubaki K, Tanaka H, Kinoshita T, Fuji K. Synthesis of the proton-ionizable lariat crown ether and chiral recognition of primary amines Tetrahedron. 58: 1679-1684. DOI: 10.1016/S0040-4020(02)00074-1 |
0.39 |
|
2001 |
Fuji K, Furuta aT, Tanaka K. Synthesis of configurationally defined sexi- and octinaphthalene derivatives. Organic Letters. 3: 169-171. PMID 11430026 DOI: 10.1021/Ol006843C |
0.312 |
|
2000 |
Kawabata T, Chen J, Suzuki H, Nagae Y, Kinoshita T, Chancharunee S, Fuji K. Memory of Chirality in Diastereoselective α-Alkylation of Isoleucine and allo-Isoleucine Derivatives Organic Letters. 2: 3883-3885. PMID 11101444 DOI: 10.1021/Ol0066274 |
0.377 |
|
2000 |
Tsubaki K, Mukoyoshi K, Otsubo T, Fuji K. The '2+1' Construction of Homooxacalix[3]arenes Possessing Different Substituents on Their Upper Rims Chemical & Pharmaceutical Bulletin. 48: 882-884. PMID 10866155 DOI: 10.1248/Cpb.48.882 |
0.377 |
|
2000 |
Kawabata T, Fuji K. Memory of Chirality. Alkylation of .ALPHA.-Amino Acid Derivatives. Journal of Synthetic Organic Chemistry Japan. 58: 1095-1099. DOI: 10.5059/Yukigoseikyokaishi.58.1095 |
0.38 |
|
2000 |
Fuji K, Ohnishi H, Moriyama S, Tanaka K, Kawabata T, Tsubaki K. Palladium-Catalyzed Asymmetric Allylic Alkylation with a Chiral Monodentate Phosphine Ligand: 8-Diphenylphosphino-8′-methoxy-1,1′-binaphthyl Synlett. 2000: 351-352. DOI: 10.1055/S-2000-6553 |
0.364 |
|
2000 |
Tsubaki K, Tanaka H, Furuta T, Kinoshita T, Fuji K. Recognition of the chain length of α,ω-diamines by a meso-ternaphthalene derivative with two crown ethers Tetrahedron Letters. 41: 6089-6093. DOI: 10.1016/S0040-4039(00)01018-2 |
0.313 |
|
2000 |
Kawabata T, Suzuki H, Nagae Y, Fuji K. A Chiral Nonracemic Enolate with Dynamic Axial Chirality: Direct Asymmetric α‐Methylation of α‐Amino Acid Derivatives Angewandte Chemie. 112: 2155-2157. DOI: 10.1002/1521-3757(20000616)112:12<2239::Aid-Ange2239>3.0.Co;2-W |
0.356 |
|
1999 |
Tanaka K, Nuruzzaman M, Yoshida M, Asakawa N, Yang X, Tsubaki K, Fuji K. Use of 1,1'-Binaphthalene-8,8'-diol as a Chiral Auxiliary for Asymmetric Michael Addition. Application to the Syntheses of Turmeronol A and B. Chemical & Pharmaceutical Bulletin. 47: 1053-1055. DOI: 10.1248/Cpb.47.1053 |
0.393 |
|
1999 |
Fuji K, Kinoshita N, Kawabata T, Tanaka K. Enantioselective Allylic Substitution Catalyzed By An Iridium Complex : Remarkable Effects Of The Counter Cation Chemical Communications. 2289-2290. DOI: 10.1039/A907680H |
0.38 |
|
1998 |
Tanaka K, Fuji K. Asymmetric Olefination Using Optically Active Phosphorous Reagents Journal of Synthetic Organic Chemistry Japan. 56: 521-531. DOI: 10.5059/Yukigoseikyokaishi.56.521 |
0.371 |
|
1998 |
Fuji K, Kawabata T, Ohmori T, Shang M, Node M. Enantioselective Creation Of Quaternary Carbon Centers Through Addition-Elimination Reaction : Asymmetric Nitroolefination Of 3-Substituted 2-Oxindole S Heterocycles. 47: 951-964. DOI: 10.3987/Com-97-S(N)107 |
0.337 |
|
1998 |
Fuji K, Oka T, Kawabata T, Kinoshita T. The first synthesis of an optically active molecular bevel gear with only two cogs on each wheel Tetrahedron Letters. 39: 1373-1376. DOI: 10.1016/S0040-4039(97)10848-6 |
0.332 |
|
1997 |
Tanaka K, Asakawa N, Nuruzzaman M, Fuji K. Use of 8,8′-dihydroxy-1,1′-binaphthalene as a chiral auxiliary for asymmetric Diels-Alder cycloadditions Tetrahedron-Asymmetry. 8: 3637-3645. DOI: 10.1016/S0957-4166(97)00474-6 |
0.402 |
|
1997 |
Tanaka K, Watanabe T, Ohta Y, Fuji K. Formation of non-racemic E- and Z-olefins based on discrimination of enantiotopic carbonyl groups in α-diketones by a chiral phosphonate reagent Tetrahedron Letters. 38: 8943-8946. DOI: 10.1016/S0040-4039(97)10328-8 |
0.347 |
|
1996 |
Tanaka K, Furuta T, Fuji K, Miwa Y, Taga T. Preparation and absolute configuration of hexahydroxyter- and octahydroxyquaternaphthalene derivatives Tetrahedron-Asymmetry. 7: 2199-2202. DOI: 10.1016/0957-4166(96)00270-4 |
0.304 |
|
1995 |
Tanaka K, Ohta Y, Fuji K. Asymmetric Michael addition reactions of chiral prop-2-enyl-and but-2-enylphosphonate anions with cyclic enones Journal of Organic Chemistry. 60: 8036-8043. DOI: 10.1021/Jo00129A051 |
0.369 |
|
1995 |
Tanaka F, Node M, Tanaka K, Mizuchi M, Hosoi S, Nakayama M, Taga T, Fuji K. 1,1′-binaphthalene-2,2′-diol as a chiral auxiliary. Diastereoselective alkylation of binaphthyl esters, complex-induced proximity effects in enolate formation, and one-step synthesis of an optically active β-substituted ketone Journal of the American Chemical Society. 117: 12159-12171. DOI: 10.1021/Ja00154A016 |
0.574 |
|
1995 |
Tanaka K, Otsubo K, Fuji K. Tandem Michael-Horner-Wadsworth-Emmons reaction of α,β-unsaturated 2,6-di-tert-butyl-4-methylphenyl esters as a convenient method for the preparation of δ-B ranched aliene carboxylates Tetrahedron Letters. 36: 9513-9514. DOI: 10.1016/0040-4039(95)02061-6 |
0.353 |
|
1994 |
Kawabata T, Fuji K. Memory of Chirality Journal of Synthetic Organic Chemistry Japan. 52: 589-595. DOI: 10.5059/Yukigoseikyokaishi.52.589 |
0.406 |
|
1994 |
Mátyus P, Fuji K, Tanaka K. Efficient and facile syntheses of [4,5]-annelated pyridazines from 4-pyridazinecarbaldehydes Heterocycles. 37: 171-174. DOI: 10.3987/Com-93-S19 |
0.324 |
|
1994 |
Fuji K, Tanaka K, Ahn M, Mizuchi M. Diastereoselectivity in Addition of Methylmagnesium Halide to Benzoylformate of Chiral 1, 1'-Binaphthalene-2, 2'-diol Chemical & Pharmaceutical Bulletin. 42: 957-959. DOI: 10.1248/Cpb.42.957 |
0.357 |
|
1994 |
Kawabata T, Wirth T, Yahiro K, Suzuki H, Fuji K. Direct Asymmetric .alpha.-Alkylation of Phenylalanine Derivatives Using No External Chiral Sources Journal of the American Chemical Society. 116: 10809-10810. DOI: 10.1021/Ja00102A066 |
0.466 |
|
1992 |
Iso Y, Yoneda F, Ikeda H, Tanaka K, Fuji K. Synthesis of viologen-tagged oligodeoxynucleotides Tetrahedron Letters. 33: 503-506. DOI: 10.1016/S0040-4039(00)93980-7 |
0.315 |
|
1992 |
Tanaka F, Fuji K. Stereochemistry of the enolate from methyl phenylacetate Tetrahedron Letters. 33: 7885-7888. DOI: 10.1016/S0040-4039(00)74769-1 |
0.522 |
|
1991 |
Node M, Itoh A, Masaki Y, Fuji K. A total synthesis of (−)-physostigmine Heterocycles. 32: 1705-1707. DOI: 10.3987/Com-91-5814 |
0.3 |
|
1991 |
Node M, Hao X, Fuji K. A Chiral Total Synthesis of (−)-Physostigmine Chemistry Letters. 20: 57-60. DOI: 10.1246/Cl.1991.57 |
0.339 |
|
1991 |
Ishikawa T, Yoneda F, Tanaka K, Fuji K. Synthesis and properties of oligothymidylate containing sulfur-modified thymidine: effect of thiation of pyrimidine ring on the thermostability and conformation of the duplex Bioorganic and Medicinal Chemistry Letters. 1: 523-526. DOI: 10.1016/S0960-894X(01)80458-3 |
0.33 |
|
1990 |
Fuji K, Kawabata T, Kiryu Y, Sugiura Y, Taga T, Miwa Y. A New Access To Chiral Aziridines By Enzymatic Transesterification Of Meso-Bis(Acetoxymethyl) Aziridines Tetrahedron Letters. 31: 6663-6666. DOI: 10.1016/S0040-4039(00)97141-7 |
0.341 |
|
1990 |
Fuji K, Node M, Tanaka F. Complex-induced proximity effects in enolate formation. Highly diastereoselective α-methylation of binaphthyl esters of arylacetic acids Tetrahedron Letters. 31: 6553-6556. DOI: 10.1016/S0040-4039(00)97115-6 |
0.507 |
|
1990 |
Fuji K, Khanapure SP, Node M, Kawabata T, ltoh A, Masaki Y. Hard acid and soft nucleophile systems. part 12. Regioselective functionalization of 1,3-dienes through the lewis acid mediated thienium cation diels-alder reaction☆☆☆ Tetrahedron. 46: 7393-7402. DOI: 10.1016/S0040-4020(01)89055-4 |
0.357 |
|
1989 |
Ochiai M, Kunishima M, Fuji K, Nagao Y. Conjugate addition of acyloxy groups to alkynylphenyliodonium tetrafluoroborates under both basic and acidic conditions. Synthesis of .alpha.-acyloxy ketones Journal of Organic Chemistry. 54: 4038-4041. DOI: 10.1021/Jo00278A012 |
0.315 |
|
1989 |
Fuji K, Node M, Tanaka F, Hosoi S. Binaphthol as a chiral auxiliary. Asymmetrical alkylation of arylacetic acid Tetrahedron Letters. 30: 2825-2828. DOI: 10.1016/S0040-4039(00)99135-4 |
0.573 |
|
1987 |
Fuji K, Node M, Kawabata T, Fujimoto M. Hard acid and soft nucleophile systems. Part 11. Hard-soft affinity inversion: dehalogenation of α-halogeno ketones with aluminium chloride and a thiol Journal of the Chemical Society-Perkin Transactions 1. 1043-1047. DOI: 10.1039/P19870001043 |
0.32 |
|
1987 |
Nagao Y, Nakiamura T, Kume M, Ochiai M, Fuji K, Fujita E. Chiral synthesis of a useful intermediate for (+)-isocarbacyclin Journal of the Chemical Society, Chemical Communications. 269-270. DOI: 10.1039/C39870000269 |
0.345 |
|
1987 |
Nagao Y, Nakamura T, Ochiai M, Fuji K, Fujita E. Synthesis of (+)-carbacyclin based on a new chiral induction procedure Journal of the Chemical Society, Chemical Communications. 267-268. DOI: 10.1039/C39870000267 |
0.364 |
|
1986 |
Fuji K, Node M, Usami Y. THE REACTION OF 2,2-DIMETHYL-4-LITHIO-1,3-OXATHIANE 3,3-DIOXIDE. GENERAL SYNTHESIS OF γ-HYDROXYKETONES Chemistry Letters. 15: 961-962. DOI: 10.1246/Cl.1986.961 |
0.384 |
|
1986 |
Fuji K, Node M, Murata M. Kinetic resolution of lactones by enantioselective protonation of the corresponding carboxylate with a chiral acid Tetrahedron Letters. 27: 5381-5382. DOI: 10.1016/S0040-4039(00)85216-8 |
0.346 |
|
1986 |
Fuji K, Node M, Nagasawa H, Naniwa Y, Terada S. Asymmetric Induction via Addition-Elimination Process: Nitroolefination of α-Substituted Lactones. Cheminform. 17. DOI: 10.1002/Chin.198643070 |
0.325 |
|
1985 |
Fuji K, Ueda M, Sumi K, Kajiwara K, Fujita E, Iwashita T, Miura I. Chemistry of carbanions stabilized by sulfur. 1. Chemistry of 1,3-oxathianes. Synthesis and conformation of 2-substituted 1,3-oxathianes Journal of Organic Chemistry. 16: 657-661. DOI: 10.1021/Jo00205A020 |
0.35 |
|
1985 |
Fuji K, Khanapure SP, Node M, Kawabata T, Ito A. Lewis acid mediated thienium cation diels-alder reaction: A new method for regio- and stereoselective functionalization of 1,3-dienes Tetrahedron Letters. 26: 779-782. DOI: 10.1016/S0040-4039(00)89135-2 |
0.383 |
|
1984 |
Node M, Kawabata T, Fujimoto M, Fuji K. General synthesis of 1-ethylthio-2-nitroolefins Synthesis. 1984: 234-236. DOI: 10.1055/S-1984-30786 |
0.301 |
|
1984 |
Node M, Kajimoto T, Nishide K, Fujita E, Fuji K. Regioselective ring opening of unsymmetrical cyclic ethers with the A1C13-NaI-acetonitrile system: Application to hydroxylation of ent-kaurene. Tetrahedron Letters. 25: 219-222. DOI: 10.1016/S0040-4039(00)99844-7 |
0.345 |
|
1984 |
Node M, Kajimoto T, Nishide K, Fujita E, Fuji K. Regioselective Ring Opening Of Unsymmetrical Cyclic Ethers With The Aluminum Trichloride-Sodium Iodide-Acetonitrile System: Application To Hydroxylation Of Ent-Kaurene Cheminform. 15. DOI: 10.1002/Chin.198419106 |
0.324 |
|
1984 |
Fuji K, Ueda M, Fujita E. 2-Lithio-2-Trimethylsilyl-1,3-Oxathiane: A Possible Acyl Dianion Equivalent Cheminform. 14: 361. DOI: 10.1002/Chin.198320217 |
0.313 |
|
1983 |
Node M, Nishide K, Kawabata T, Ohta K, Watanabe K, Fuji K, Fujita E. Hard acid and soft nucleophile system. VII. A convenient reduction of functionalized polyarenes to parent polyarenes. Chemical & Pharmaceutical Bulletin. 31: 4306-4311. DOI: 10.1248/Cpb.31.4306 |
0.307 |
|
1983 |
Fuji K, Ueda M, Fujita E. 2-Lithio-2-trimethylsilyl-1,3-oxathian: a possible acyl dianion equivalent Journal of the Chemical Society, Chemical Communications. 49-50. DOI: 10.1039/C39830000049 |
0.312 |
|
1982 |
Node M, Nishide K, Ochiai M, Fuji K, Fujita E. Hard Acid And Soft Nucleophile Systems. 5. Ring-Opening Reaction Of Lactones To Ω-Alkylthio- Or Ω-Arylthio Carboxylic Acids With Aluminum Halide And Thiol Cheminform. 13. DOI: 10.1002/Chin.198222121 |
0.339 |
|
1981 |
Node M, Nishide K, Ochiai M, Fuji K, Fujita E. Hard acid and soft nucleophile systems. 5. Ring-opening reaction of lactones to .omega.-alkylthio- or .omega.-arylthio carboxylic acids with aluminum halide and thiol Journal of Organic Chemistry. 46: 5163-5166. DOI: 10.1021/Jo00338A020 |
0.331 |
|
1981 |
Fuji K, Ueda M, Sumi K, Fujita E. Synthesis of 2-heterosubstituted 1,3-oxathianes and their reaction with sec- butyllithium Tetrahedron Letters. 22: 2005-2008. DOI: 10.1016/S0040-4039(01)92890-4 |
0.312 |
|
1981 |
Fuji K, Ueda M, Sumi K, Fujita E. 2-Ethylthio-1,3-Benzodithiole : A Methoxycarbonyl Anion Equivalent. A General Synthesis of α-Hydroxy Esters Cheminform. 12: 209-215. DOI: 10.1002/Chin.198142178 |
0.34 |
|
1981 |
Fuji K, Ueda M, Kajiwara K, Sumi K, Fujita E, Miura I. Synthesis of 2-Heterosubstituted 1,3-Oxathianes and Their Reactions with Strong Bases Cheminform. 12: 178. DOI: 10.1002/Chin.198129259 |
0.322 |
|
1980 |
Fuji K, Kawabata T, Fujita E. Hard acid and soft nucleophile system. IV. Removal of benzyl protecting group with boron trifluoride etherate and dimethyl sulflide. Chemical & Pharmaceutical Bulletin. 28: 3662-3664. DOI: 10.1248/Cpb.28.3662 |
0.328 |
|
1980 |
Fuji K, Ichikawa K, Fujita E. Lythraceous alkaloids. Part 11. Total synthesis of (±)-lythranidine Journal of the Chemical Society-Perkin Transactions 1. 11: 1066-1069. DOI: 10.1039/P19800001066 |
0.335 |
|
1980 |
Node M, Nishide K, Fuji K, Fujita E. Hard acid and soft nucleophile system. 2. Demethylation of methyl ethers of alcohol and phenol with an aluminum halide-thiol system Journal of Organic Chemistry. 12: 4275-4277. DOI: 10.1021/Jo01310A003 |
0.301 |
|
1980 |
Fuji K, Ichikawa K, Fujita E. A Versatile Synthesis Of (.+-.)-Solenopsin A Cheminform. 11. DOI: 10.1002/Chin.198019223 |
0.329 |
|
1980 |
Node M, Nishide K, Sai M, Ichikawa K, Fuji K, Fujita E. Aluminium Halide-Thiol System: A Useful Reagent For Demethylation Of Aliphatic And Aromatic Methyl Ethers And Demethylation Of Methylenedioxy Compounds Cheminform. 11. DOI: 10.1002/Chin.198006156 |
0.324 |
|
1979 |
Node M, Nishide K, Sai M, Ichikawa K, Fuji K, Fujita E. Aluminium halide-thiol system: A useful reagent for demethylation of aliphatic and aromatic methyl ethers and demethylenation of methylenedioxy compounds. Chemistry Letters. 8: 97-98. DOI: 10.1246/Cl.1979.97 |
0.331 |
|
1979 |
Fuji K, Ichikawa K, Node M, Fujita E. Hard acid and soft nucleophile system. New efficient method for removal of benzyl protecting group Journal of Organic Chemistry. 44: 1661-1664. DOI: 10.1021/Jo01324A017 |
0.349 |
|
1979 |
Fuji K, Ichikawa K, Fujita E. Total synthesis of a cyclophane alkaloid, (+/-)-lythranidine Tetrahedron Letters. 20: 361-364. DOI: 10.1016/S0040-4039(01)85971-2 |
0.336 |
|
1979 |
Fuji K, Ichikawa K, Node M, Fujita E. Hard Acid And Soft Nucleophile System. New Efficient Method For Removal Of Benzyl Protecting Group Cheminform. 10. DOI: 10.1002/Chin.197938113 |
0.31 |
|
1978 |
Fuji K, Ueda M, Fujita E. Alkylation Of 1,3-Oxathiane Cheminform. 9. DOI: 10.1002/Chin.197810230 |
0.384 |
|
1977 |
Fuji K, Ueda M, Fujita E. Alkylation of 1,3-oxathian Journal of the Chemical Society, Chemical Communications. 814-814. DOI: 10.1039/C39770000814 |
0.384 |
|
1975 |
KUTNEY JP, COOK J, FUJI K, TREASURYWALA AM, CLARDY J, FAYOS J, WRIGHT C. ChemInform Abstract: STUDIES ON THE SYNTHESIS OF BISINDOLE ALKALOIDS. THE SYNTHESIS, STRUCTURE AND ABSOLUTE CONFIGURATION OF 18′-EPI-4′-DEOXO-EPIVINBLASTINE, 18′-DECARBOMETHOXY-18′-EPI-4′-EPIVINBLASTINE AND 18′-EPI-3′,4′-DEHYDROVINBLASTINE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197532395 |
0.347 |
|
1966 |
Fujita E, Fujita T, Fuji K, Ito N. Terpenoids—II : The chemical conversion of enmein into (−)-Kaurane—the absolute configuration of enmein Tetrahedron. 22: 3423-3441. DOI: 10.1016/S0040-4020(01)92532-3 |
0.353 |
|
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