| Year |
Citation |
Score |
| 2010 |
KOREEDA M, YANG W. ChemInform Abstract: The Chemistry of 1,2-Dithiins: Synthesis of 1,2-Dithiin and 3,6- Disubstituted 1,2-Dithiins. Cheminform. 25: no-no. DOI: 10.1002/chin.199435178 |
0.346 |
|
| 2010 |
KOREEDA M, DIXON LA, HSI JD. ChemInform Abstract: An Efficient Formal Synthesis of Aflatoxin B2 by Use of the Kikuchi Rearrangement Reaction. Cheminform. 25: no-no. DOI: 10.1002/chin.199410107 |
0.301 |
|
| 2010 |
GIMISIS T, KAMPF JW, KOREEDA M. ChemInform Abstract: Synthesis of Methylene-Bridged Polycyclic Aromatic Hydrocarbons: An Efficient, Double Friedel-Crafts Cyclization Approach to 11H-Benz(bc) aceanthrylene (VII). Cheminform. 25: no-no. DOI: 10.1002/chin.199407131 |
0.688 |
|
| 2010 |
KOREEDA M, JUNG K, HIROTA M. ChemInform Abstract: A Novel Regio- and Stereocontrolled Synthesis of Diol Epoxide and trans-Dihydrodiol Metabolites of Polycyclic Aromatic Hydrocarbons. An Application to the Synthesis of the Bay-Region syn- and anti-Diol Epoxides of the Carcinogen 1,4-D Cheminform. 22: no-no. DOI: 10.1002/chin.199102181 |
0.323 |
|
| 2009 |
Houston TA, Koreeda M. Iodine-promoted ribosylation leads to a facile acetonide-forming reaction. Carbohydrate Research. 344: 2240-4. PMID 19765691 DOI: 10.1016/J.Carres.2009.08.026 |
0.348 |
|
| 2004 |
Zhang L, Koreeda M. Radical deoxygenation of hydroxyl groups via phosphites. Journal of the American Chemical Society. 126: 13190-1. PMID 15479050 DOI: 10.1021/Ja0462777 |
0.452 |
|
| 2004 |
Holtsclaw J, Koreeda M. A ring-rearrangement metathesis approach toward the synthesis of cyclopenta- and cyclohexa[c]indene systems. Organic Letters. 6: 3719-22. PMID 15469332 DOI: 10.1021/Ol048650L |
0.722 |
|
| 2004 |
Zhang L, Koreeda M. Total synthesis of (+)-acanthodoral by the use of a Pd-catalyzed metal-ene reaction and a nonreductive 5-exo-acyl radical cyclization. Organic Letters. 6: 537-40. PMID 14961617 DOI: 10.1021/Ol0363063 |
0.533 |
|
| 2002 |
Zhang L, Koreeda M. Stereocontrolled synthesis of kelsoene by the homo-favorskii rearrangement. Organic Letters. 4: 3755-8. PMID 12375936 DOI: 10.1021/Ol026739Q |
0.568 |
|
| 2002 |
Koreeda M, Wang Y, Zhang L. 6-Exo-spiro (alkoxycarbonylamino)methyl radical cyclization: highly regio- and stereoselective synthesis of (-)-sibirine. Organic Letters. 4: 3329-32. PMID 12227781 DOI: 10.1021/Ol026671E |
0.537 |
|
| 2002 |
Chervin SM, Lowe JB, Koreeda M. Synthesis and biological evaluation of a new sialyl Lewis X mimetic derived from lactose. The Journal of Organic Chemistry. 67: 5654-62. PMID 12153264 DOI: 10.1021/Jo025579T |
0.75 |
|
| 2000 |
Chervin SM, Abada P, Koreeda M. Convenient, in situ generation of anhydrous hydrogen iodide for the preparation of alpha-glycosyl iodides and vicinal iodohydrins and for the catalysis of Ferrier glycosylation Organic Letters. 2: 369-72. PMID 10814325 DOI: 10.1021/Ol991312D |
0.761 |
|
| 2000 |
Chervin SM, Abada P, Koreeda M. Convenient, in situ generation of anhydrous hydrogen iodide for the preparation of α-glycosyl iodides and vicinal lodohydrins and for the catalysis of Ferrier glycosylation Organic Letters. 2: 369-372. |
0.749 |
|
| 1998 |
Wang Y, Koreeda M, Chatterji T, Gates KS. Total synthesis and DNA-cleaving properties of thiarubrine C Journal of Organic Chemistry. 63: 8644-8645. DOI: 10.1021/Jo981849P |
0.318 |
|
| 1997 |
Shull BK, Sakai T, Nichols JB, Koreeda M. Mitsunobu Reaction of Unbiased Cyclic Allylic Alcohols. The Journal of Organic Chemistry. 62: 8294-8303. PMID 11671964 DOI: 10.1021/Jo9615155 |
0.34 |
|
| 1997 |
Koreeda M, Wang Y. Novel Synthesis of 3,6-Disubstituted 1,2-Dithiin Molecules Involving a Direct Oxidative Deprotection-Cyclization Sequence from 1,4-Bis(tert-butylthio)- 1,3-butadiene Precursors. The Journal of Organic Chemistry. 62: 446-447. PMID 11671429 DOI: 10.1021/Jo962109O |
0.36 |
|
| 1996 |
Shull BK, Wu Z, Koreeda M. A convenient, highly efficient one-pot preparation of peracetylated glycals from reducing sugars Journal of Carbohydrate Chemistry. 15: 955-964. DOI: 10.1080/07328309608005701 |
0.366 |
|
| 1996 |
Shull BK, Sakai T, Koreeda M. Eu(fod)3-catalyzed rearrangement of allylic methoxyacetates Journal of the American Chemical Society. 118: 11690-11691. DOI: 10.1021/Ja962718D |
0.421 |
|
| 1996 |
Koreeda M, Gopalaswamy R, Yang J, Tuinman RJ. Stereocontrolled synthesis of syn- and anti-diol epoxide metabolites of triphenylene Tetrahedron Letters. 37: 8267-8270. DOI: 10.1016/0040-4039(96)01896-5 |
0.425 |
|
| 1996 |
Gopalaswamy R, Koreeda M. On the mechanism of the stereo- and regioselective ether-ring opening of 1,2,3,4-tetrahydro-1β,4β-epoxy-2α,3α-carbonyldioxy arene systems with boron tribromide Tetrahedron Letters. 37: 3651-3654. DOI: 10.1016/0040-4039(96)00664-8 |
0.339 |
|
| 1996 |
Wu J, Shull BK, Koreeda M. 1-[2-(Trimethylsilyl)ethoxy]ethyl (SEE): A novel hybrid hydroxy-protecting group between 1-(ethoxy)ethyl (EE) and 2-(trimethylsilyl)ethoxymethyl (SEM) Tetrahedron Letters. 37: 3647-3650. DOI: 10.1016/0040-4039(96)00663-6 |
0.325 |
|
| 1995 |
Koreeda M, Gopalaswamy R. Stereo- and regiocontrolled synthesis of bay region syn- and anti-diol epoxide metabolites of carcinogenic polycyclic aromatic hydrocarbons Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 53: 1033-1044. DOI: 10.5059/Yukigoseikyokaishi.53.1033 |
0.376 |
|
| 1995 |
Koreeda M, Wu J. Stereoselective Synthesis of the Brassinolide Side Chain by the Use of a 5-Exo-α-Silyl Radical Cyclization - Protiodesilylation Sequence Synlett. 1995: 850-852. DOI: 10.1055/S-1995-5095 |
0.439 |
|
| 1995 |
Koreeda M, Houston TA, Shull BK, Klemke E, Tuinman RJ. Iodine-catalyzed Ferrier Reaction 1. A Mild and Highly Versatile Glycosylation of Hydroxyl and Phenolic Groups1 Synlett. 1995: 90-92. DOI: 10.1055/S-1995-4873 |
0.395 |
|
| 1995 |
Koreeda M, Gopalaswamy R. Regio- and stereocontrolled synthesis of the bay-region anti-diol epoxide metabolites of the potent carcinogens benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene Journal of the American Chemical Society. 117: 10595-10596. DOI: 10.1021/Ja00147A031 |
0.367 |
|
| 1994 |
Houston TA, Koreeda M. Stereochemical dependence of the bis-alkylation reaction of α,α- dilithiated allyl phenyl sulfone with cis- and trans-1,4-dichloro-2-butene. A convenient method for the synthesis of a cyclohepta-1,4-diene system Synthetic Communications. 24: 393-398. DOI: 10.1080/00397919408011198 |
0.45 |
|
| 1994 |
Koreeda M, Yang W. The Chemistry of 1,2-Dithiins: Synthesis of 1,2-Dithiin and 3,6-Disubstituted 1,2-Dithiins Synlett. 1994: 201-203. DOI: 10.1055/S-1994-22794 |
0.448 |
|
| 1994 |
Koreeda M, Yang W. Chemistry of 1,2-dithiins. Synthesis of the potent antibiotic thiarubrine A Journal of the American Chemical Society. 116: 10793-10794. DOI: 10.1021/Ja00102A058 |
0.386 |
|
| 1993 |
Koreeda M, Dixon LA, Hsi JD. An Efficient Formal Synthesis of Aflatoxin B2 by Use of the Kikuchi Rearrangement Reaction Synlett. 1993: 555-556. DOI: 10.1055/S-1993-22526 |
0.403 |
|
| 1993 |
Gimisis T, Koreeda M. A highly efficient synthesis of 3-methylcholanthrene Journal of Organic Chemistry. 58: 7158-7161. DOI: 10.1021/Jo00077A045 |
0.711 |
|
| 1993 |
Gimisis T, Kampf JW, Koreeda M. Synthesis of methylene-bridged polycyclic aromatic hydrocarbons: An efficient, double Friedel-Crafts cyclization approach to 11H-benz[bc]aceanthrylene Journal of Organic Chemistry. 58: 5858-5861. DOI: 10.1021/Jo00073A058 |
0.7 |
|
| 1993 |
Houston TA, Tanaka Y, Koreeda M. Stereoselective construction of 22-oxygenated steroid side chains by dimethylaluminum chloride-mediated ene reactions of aldehydes Journal of Organic Chemistry. 58: 4287-4292. DOI: 10.1021/Jo00068A024 |
0.417 |
|
| 1993 |
You Z, Koreeda M. A [2,3]-Wittig rearrangement that requires severe deformation from a stable 6-membered ring chair structure and its application to synthesize 1,3-anti-3,5-anti-1,3,5-trimethylated carbon chain compounds Tetrahedron Letters. 34: 2597-2600. DOI: 10.1016/S0040-4039(00)77634-9 |
0.37 |
|
| 1993 |
You Z, Koreeda M. Axial selectivity of 1,2-nucleophilic additions to 2-(Alkylidene)cyclohexanones: Is it higher than that of 2-cyclohexenones? Tetrahedron Letters. 34: 2745-2748. DOI: 10.1016/S0040-4039(00)73551-9 |
0.34 |
|
| 1992 |
Woski SA, Koreeda M. Synthesis of the putative active metabolites of the cyclopenta[a]phenanthrenes. Synthesis of the trans-3,4-dihydro 3,4-diol and syn-3,4-diol 1,2-epoxide derivatives of the mutagen 15,16-dihydrocyclopenta[a]phenanthren-17-one Journal of Organic Chemistry. 57: 5736-5741. DOI: 10.1021/Jo00047A030 |
0.761 |
|
| 1992 |
Yang W, Koreeda M. The stereocontroiled synthesis of phthalic acid 4,5-cis-dihydrodiol. An unambiguous structural assignment of the bacterial metabolite of phthalic acid Journal of Organic Chemistry. 57: 3836-3839. DOI: 10.1021/Jo00040A023 |
0.405 |
|
| 1992 |
Hamann LG, Guider AM, Koreeda M. An efficient, highly stereoselective synthesis of (Z)-16.alpha.-hydroxy-17-ethylidene steroids Journal of Organic Chemistry. 57: 3507-3509. DOI: 10.1021/Jo00038A052 |
0.403 |
|
| 1992 |
Koreeda M, Visger DC. On the factors that affect the mode of cyclization of α-silyl radicals: A method for angular hydroxymethylation by the 5-exo cyclization Tetrahedron Letters. 33: 6603-6606. DOI: 10.1016/S0040-4039(00)60996-6 |
0.385 |
|
| 1992 |
Li K, Hamann LG, Koreeda M. A convenient, highly stereoselective synthesis of anti-α,β-epoxy alcohols by the Luche reduction of α,β-epoxy ketones Tetrahedron Letters. 33: 6569-6570. DOI: 10.1016/S0040-4039(00)60987-5 |
0.317 |
|
| 1992 |
Hamann LG, Guider AM, Koreeda M. An efficient, highly stereoselective synthesis of (Z)-16α-hydroxy-17-ethylidene steroids Journal of Organic Chemistry. 57: 3507-3509. |
0.321 |
|
| 1991 |
Valdés LJ, Koreeda M. Synthesis of the 6-benzoyl derivative of 1-deoxy-1-oxo-7-desacetylforskolin and an unambiguous assignment of the absolute stereochemistry of forskolin Journal of Organic Chemistry. 56: 844-846. DOI: 10.1021/Jo00002A064 |
0.452 |
|
| 1991 |
Jin Kim S, Harris CM, Jung KY, Koreeda M, Harris TM. Non-biomimetic route to deoxyadenosine adducts of carcinogenic polycyclic aromatic hydrocarbons Tetrahedron Letters. 32: 6073-6076. DOI: 10.1016/0040-4039(91)80756-V |
0.407 |
|
| 1990 |
Koreeda M, George IA. Stereocontrolled Synthesis of (22R)-22-Hydroxycholesterol Guided by α-Silyl Radical Stabilization Chemistry Letters. 19: 83-86. DOI: 10.1246/Cl.1990.83 |
0.426 |
|
| 1990 |
Koreeda M, Brown L, Valdés III LJ. The Absolute Stereochemistry of Salvinorins Chemistry Letters. 19: 2015-2018. DOI: 10.1246/Cl.1990.2015 |
0.335 |
|
| 1990 |
Shull BK, Koreeda M. Halogen effect on the ring opening of pulegone hydrohalides Journal of Organic Chemistry. 55: 2249-2251. DOI: 10.1021/Jo00294A054 |
0.308 |
|
| 1990 |
Shull BK, Koreeda M. Reduction of 17.alpha.-hydroxy-20-keto steroids: convenient synthesis of (E)-3.beta.-hydroxy-5,17(20)-pregnadiene 3-pivaloate and (Z)-3.beta.,16.alpha.-dihydroxy-5,17(20)-pregnadiene 3-pivaloate The Journal of Organic Chemistry. 55: 99-105. DOI: 10.1021/Jo00288A021 |
0.343 |
|
| 1990 |
Koreeda M, Hamann LG. Chirality transmission involving a free-radical-mediated 6-exo cyclization process. Stereocontrolled synthesis of branched-chain 1,4-diols Journal of the American Chemical Society. 112: 8175-8177. DOI: 10.1021/Ja00178A057 |
0.406 |
|
| 1990 |
Koreeda M, Jung KY, Hirota M. A novel regio- and stereocontrolled synthesis of diol epoxide and trans-dihydriol metabolites of polycyclic aromatic hydrocarbons. An application to the synthesis of the bay-region syn- and anti-diol epoxides of the carcinogen 1,4-dimethylphenanthrene Journal of the American Chemical Society. 112: 7413-7414. DOI: 10.1021/Ja00176A062 |
0.414 |
|
| 1990 |
Koreeda M, Teng K, Murata T. (1E,3E)-4-acetoxy-1-phenyldimethylsilyl-1,3-butadiene as a surrogate for (1E,3E)-1,4- diacetoxy-1,3-butadiene: a highly efficient synthesis of (±)-shikimic acid Tetrahedron Letters. 31: 5997-6000. DOI: 10.1016/S0040-4039(00)98012-2 |
0.37 |
|
| 1990 |
Koreeda M, Koo S. 1,2-Addition of dimethyl(phenyl)silyllithium to cyclic α,β-unsaturated ketones and regiospecific generation of cyclic silyl enol ethers through brook rearrangement of the 1,2-addition products Tetrahedron Letters. 31: 831-834. DOI: 10.1016/S0040-4039(00)94639-2 |
0.413 |
|
| 1989 |
Sinsheimer JE, Giri AK, Messerly EA, Jung KY, Koreeda M. Mutagenicity in Salmonella and sister chromatid exchange in mice for the bay-region syn- and anti-diol epoxides of 1,4-dimethylphenanthrene. Carcinogenesis. 10: 1123-6. PMID 2655964 DOI: 10.1093/Carcin/10.6.1123 |
0.314 |
|
| 1989 |
Koreeda M, Jung KY, Ichita J. Diels-Alder reactions of 3,4-dialkoxyfurans: An application to the highly efficient synthesis of (±)-methyl triacetylshikimate Journal of the Chemical Society, Perkin Transactions 1. 2129-2131. DOI: 10.1039/P19890002129 |
0.381 |
|
| 1989 |
Jung K, Koreeda M. Synthesis of 1,4-, 2,4-, and 3,4-dimethylphenanthrenes: A novel deoxygenation of arene 1,4-endoxides with trimethylsilyl iodide Journal of Organic Chemistry. 54: 5667-5675. DOI: 10.1021/Jo00285A011 |
0.479 |
|
| 1989 |
Hsi JD, Koreeda M. Reactions of a semistabilized arsonium ylide with aldehydes: Counterion effects on product selectivity Journal of Organic Chemistry. 54: 3229-3231. DOI: 10.1021/Jo00274A057 |
0.323 |
|
| 1989 |
Mase T, Ichita J, Marino JP, Koreeda M. The total synthesis of the water mold sex hormone oogoniol Tetrahedron Letters. 30: 2075-2078. DOI: 10.1016/S0040-4039(01)93715-3 |
0.367 |
|
| 1988 |
Koreeda M, Ricca DJ, Luengo JI. Synthesis of (±)-verrucarol using a remarkably facile alumina-catalyzed intramolecular Diels-Alder reaction Journal of Organic Chemistry. 53: 5586-5588. DOI: 10.1021/Jo00258A049 |
0.39 |
|
| 1987 |
Koreeda M, Tanaka Y. Stereoselective acyclic synthesis via allylmetals: Threo vicinal diols from both E- and Z-γ-alkoxyallyltins and aldehydes Tetrahedron Letters. 28: 143-146. DOI: 10.1016/S0040-4039(00)95670-3 |
0.354 |
|
| 1986 |
Koreeda M, Ricca DJ. Chirality transfer in stereoselective synthesis. A highly stereocontrolled synthesis of 22-hydroxylated steroid side chains via the [2,3]-wittig rearrangement Journal of Organic Chemistry. 51: 4090-4092. DOI: 10.1021/Jo00371A042 |
0.436 |
|
| 1986 |
Koreeda M, George IA. Chirality transmission via a 6-endo free-radical-mediated cyclization process. Regio- and stereocontrolled synthesis of the 22-hydroxylated steroid side chains Journal of the American Chemical Society. 108: 8098-8100. DOI: 10.1021/Ja00285A042 |
0.39 |
|
| 1986 |
KOREEDA M, HULIN B, YOSHIHARA M, TOWNSEND CA, CHRISTENSEN SB. ChemInform Abstract: Synthesis and Absolute Configuration of (+)-Averufin (I). Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198623349 |
0.435 |
|
| 1985 |
Frantz SW, van den Eeckhout E, Sinsheimer JE, Yoshihara M, Koreeda M. Mutagenicity in Salmonella assays of cyclohexane epoxide derivatives. Toxicology Letters. 25: 265-71. PMID 4012804 DOI: 10.1016/0378-4274(85)90206-1 |
0.321 |
|
| 1985 |
Koreeda M, Hulin B, Yoshihara M, Townsend CA, Christensen SB. Synthesis and absolute configuration of (+)-averufin Journal of Organic Chemistry. 50: 5426-5428. DOI: 10.1021/Jo00225A098 |
0.431 |
|
| 1985 |
Koreeda M, Luengo JI. The anionic oxy-claisen rearrangement of enolates of .alpha.-allyloxy ketones. A remarkable rate accelerating effect exhibited by the nature of the counterion Journal of the American Chemical Society. 107: 5572-5573. DOI: 10.1021/Ja00305A066 |
0.331 |
|
| 1984 |
Luengo JI, Koreeda M. Stereospecific synthesis of Z- and E-1 alkoxy-1,3-butadienes Tetrahedron Letters. 25: 4881-4884. DOI: 10.1016/S0040-4039(01)91249-3 |
0.415 |
|
| 1984 |
Brown L, Koreeda M. Benzoyl trifluoromethanesulfonate. A mild reagent for the benzoylation of sterically hindered hydroxyls Journal of Organic Chemistry. 49: 3875-3880. DOI: 10.1002/Chin.198514158 |
0.439 |
|
| 1984 |
Koreeda M, Luengo JI. A novel type of intramolecular diels-alder reaction involving dienol ethers: An unusual preference for a boat transition state in the incipient ring formation [5] Journal of Organic Chemistry. 49: 2079-2081. DOI: 10.1002/Chin.198452076 |
0.356 |
|
| 1984 |
Hulin B, Koreeda M. A convenient, mild method for the cyclization of 3- and 4-arylalkanoic acids via their trifluoromethanesulfonic anhydride derivatives Journal of Organic Chemistry. 49: 207-209. DOI: 10.1002/Chin.198425164 |
0.34 |
|
| 1983 |
Koreeda M, Brown L. Benzoyl trifluoromethanesulphonate. A highly efficient benzoylating agent for sterically hindered hydroxy groups Journal of the Chemical Society, Chemical Communications. 1113-1115. DOI: 10.1039/C39830001113 |
0.374 |
|
| 1983 |
Koreeda M, Brown L. Chirality transfer in stereoselective synthesis. A highly stereoselective synthesis of optically active vitamin E side chains Journal of Organic Chemistry. 48: 2122-2124. DOI: 10.1021/Jo00160A047 |
0.376 |
|
| 1983 |
Koreeda M, Mislankar SG. Chemistry of the dianions of 3-heteroatom-substituted cyclopent-2-en-1-ones: An expedient route to dl-coriolin Journal of the American Chemical Society. 105: 7203-7205. DOI: 10.1002/Chin.198409348 |
0.408 |
|
| 1983 |
KOREEDA M, TANAKA Y. ChemInform Abstract: STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: STRUCTURAL DEPENDENCE IN A LEWIS-ACID CATALYZED ADDITION OF ALLYLTINS TO ALDEHYDES Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198306153 |
0.318 |
|
| 1983 |
KOREEDA M, TANAKA Y. ChemInform Abstract: STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: AN EFFICIENT SYNTHESIS OF (.+-.)-4-METHYLHEPTAN-3-OL, AN AGGREGATION PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198306131 |
0.326 |
|
| 1982 |
Koreeda M, Tanaka Y. Stereoselective acyclic synthesis via allylmetals: Vicinal diols from γ-alkoxyallylaluminium compounds and aldehydes or ketones Journal of the Chemical Society, Chemical Communications. 845-847. DOI: 10.1039/C39820000845 |
0.449 |
|
| 1982 |
Koreeda M, Ciufolini MA. Natural product synthesis via allylsilanes. 1. Synthesis and reactions of (1E,3E)-4-acetoxy-1-(trimethylsilyl)-1,3-butadiene and its use in the total synthesis of (±)-shikimic acid Journal of the American Chemical Society. 104: 2308-2310. DOI: 10.1021/Ja00372A034 |
0.616 |
|
| 1982 |
Koreeda M, Tanaka Y. STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: STRUCTURAL DEPENDENCE IN A LEWIS-ACID CATALYZED ADDITION OF ALLYLTINS TO ALDEHYDES Chemistry Letters. 11: 1299-1302. DOI: 10.1002/Chin.198306153 |
0.418 |
|
| 1982 |
Koreeda M, Tanaka Y. STEREOSELECTIVE ACYCLIC SYNTHESIS VIA ALLYLMETALS: AN EFFICIENT SYNTHESIS OF (±)-4-METHYLHEPTAN-3-OL, AN AGGREGATION PHEROMONE OF THE SMALLER EUROPEAN ELM BARK BEETLE Chemistry Letters. 11: 1297-1298. DOI: 10.1002/Chin.198306131 |
0.376 |
|
| 1981 |
Koreeda M, Yoshihara M. The absolute configurations of anti-benzene and anti-naphthalene 1,2:3,4-dioxides Journal of the Chemical Society, Chemical Communications. 974-976. DOI: 10.1039/C39810000974 |
0.311 |
|
| 1981 |
Koreeda M, Chen YPL. Synthesis of (±)-desepoxy-4,5-didehydromethylenomycin A Tetrahedron Letters. 22: 15-18. DOI: 10.1016/0040-4039(81)80028-7 |
0.308 |
|
| 1981 |
KOREEDA M, CHEN YPL. ChemInform Abstract: SYNTHESIS OF (.+-.)-DEEPOXY-4,5-DIDEHYDROMETHYLENOMYCIN A Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198117375 |
0.329 |
|
| 1980 |
Koreeda M, Tanaka Y, Schwartz A. Stereochemically controlled synthesis of steroid side chains: Synthesis of desmosterol Journal of Organic Chemistry. 45: 1172-1174. DOI: 10.1021/Jo01294A056 |
0.386 |
|
| 1980 |
Koreeda M, Akagi H. A convenient synthesis of substituted γ-pyrones Tetrahedron Letters. 21: 1197-1200. DOI: 10.1016/S0040-4039(00)71369-4 |
0.405 |
|
| 1980 |
Hayashi Y, Matsumoto T, Uemura M, Koreeda M. Carbon-13 NMR studies of the biologically active nor-diterpenoid dilactones fromPodocarpus plants Organic Magnetic Resonance. 14: 86-91. DOI: 10.1002/Mrc.1270140203 |
0.322 |
|
| 1979 |
Koreeda M, Liang Y, Akagi H. Easy generation of the dianions of 3-isobutoxycyclopent-2-en-1-ones and their reactions Journal of the Chemical Society, Chemical Communications. 449-450. DOI: 10.1039/C39790000449 |
0.411 |
|
| 1979 |
KOREEDA M, LIANG Y, AKAGI H. ChemInform Abstract: EASY GENERATION OF THE DIANIONS OF 3-ISOBUTOXYCYCLOPENT-2-EN-1-ONES AND THEIR REACTIONS Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197947169 |
0.356 |
|
| 1978 |
Teicher BA, Koizumi N, Koreeda M, Shikita M, Talalay P. Biosynthesis of pregnenolone from cholesterol by mitochondrial enzymes of bovine adrenal cortex. The question of the participation of the 20(22)-olefins and 20, 22-epoxides of cholesterol. European Journal of Biochemistry / Febs. 91: 11-9. PMID 720329 DOI: 10.1111/J.1432-1033.1978.Tb20931.X |
0.303 |
|
| 1977 |
Yagi H, Akagi H, Thakker DR, Mah HD, Koreeda M, Jerina DM. Absolute sterochemistry of the highly mutagenic 7,8-diol 9,10-epoxides derived from the potent carcinogen trans-7,8-dihydroxy-7,8-dihydrobenzol[a]pyrene. Journal of the American Chemical Society. 99: 2358-9. PMID 864141 DOI: 10.1002/Chin.197725111 |
0.395 |
|
| 1977 |
Yagi H, Thakker DR, Hernandez O, Koreeda M, Jerina DM. Synthesis and reactions of the highly mutagenic 7,8-diol 9,10-epoxides of the carcinogen benzo[a]pyrene. Journal of the American Chemical Society. 99: 1604-11. PMID 839009 DOI: 10.1021/Ja00447A053 |
0.449 |
|
| 1977 |
Yagi H, Thakker D, Hernandez O, Koreeda M, Jerina D. Additions and Corrections - Synthesis and Reactions of the highly Mutagenic 7,8-Diol 9,10-Epoxides of the Carcinogen Benzo[a]pyrene Journal of the American Chemical Society. 99: 5228-5228. DOI: 10.1021/Ja00457A604 |
0.443 |
|
| 1977 |
YAGI H, AKAGI H, THAKKER DR, MAH HD, KOREEDA M, JERINA DM. ChemInform Abstract: ABSOLUTE STEREOCHEMISTRY OF THE HIGHLY MUTAGENIC 7,8-DIOL 9,10-EPOXIDES DERIVED FROM THE POTENT CARCINOGEN TRANS-7,8-DIHYDROXY-7,8-DIHYDROBENZO(A)PYRENE Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197725111 |
0.304 |
|
| 1977 |
Yagi H, Thakker DR, Hernandez O, Koreeda M, Jerina DM. Synthesis And Reactions Of The Highly Mutagenic 7,8‐Diol 9,10‐Epoxides Of The Carcinogen Benzo(A)Pyrene Cheminform. 8. DOI: 10.1002/Chin.197721193 |
0.432 |
|
| 1976 |
Koreeda M, Koizumi N, Teicher BA. Stereospecific synthesis of (Z)-20(22)-didehydrocholesterol Journal of the Chemical Society, Chemical Communications. 1035-1036. DOI: 10.1002/Chin.197716353 |
0.407 |
|
| 1975 |
Varma RK, Koreeda M, Yagen B, Nakanishi K, Caspi E. Synthesis and C-25 chirality of 26-hydroxycholesterols. The Journal of Organic Chemistry. 40: 3680-6. PMID 1195040 DOI: 10.1021/Jo00913A014 |
0.531 |
|
| 1974 |
Koreeda M, Harada N, Nakanishi K. Exciton chirality methods as applied to conjugated enones, esters, and lactones Journal of the American Chemical Society. 96: 266-268. DOI: 10.1021/Ja00808A053 |
0.482 |
|
| 1974 |
Koreeda M, Harada N, Nakanishi K. Exciton chirality methods as applied to conjugated enones, esters, and lactones Cheminform. 5. DOI: 10.1002/Chin.197412095 |
0.482 |
|
| 1974 |
Koreeda M, Harada N, Nakanishi K. Exciton chirality method as applied to conjugated enones, esters, and lactones [14] Journal of the American Chemical Society. 96: 266-268. |
0.408 |
|
| 1973 |
Weiss G, Koreeda M, Nakanishi K. Stereochemistry of theaspirone and the blumenols Journal of the Chemical Society, Chemical Communications. 565-566. DOI: 10.1039/C39730000565 |
0.379 |
|
| 1973 |
Koreeda M, Weiss G, Nakanishi K. Absolute configuration of natural (+)-abscisic acid Journal of the American Chemical Society. 95: 239-240. DOI: 10.1021/Ja00782A043 |
0.408 |
|
| 1973 |
KOREEDA M, WEISS G, NAKANISHI K. ChemInform Abstract: ABSOLUTE KONFIG. VON NATUERLICHER (+)-ABSCISSAEURE Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197311086 |
0.429 |
|
| 1972 |
Nakanishi K, Schooley DA, Koreeda M, Miura I. General method for distinguishing threo and erythro isomers of certain .alpha.-glycols and related compounds Journal of the American Chemical Society. 94: 2865-2867. DOI: 10.1021/Ja00763A058 |
0.432 |
|
| 1972 |
NAKANISHI K, SCHOOLEY DA, KOREEDA M, MIURA I. ChemInform Abstract: ALLGEMEINE METHODE ZUR UNTERSCHEIDUNG VON THREO- UND ERYTHRO-ISOMEREN BESTIMMTER ALPHA-GLYKOLE UND VERWANDTER VERBINDUNGEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197228081 |
0.421 |
|
| 1971 |
Koreeda M, Schooley DA, Nakanishi K, Hagiwara H. The absolute configurations at C-20 and C-22 in ecdysones. Journal of the American Chemical Society. 93: 4084-5. PMID 5138311 |
0.338 |
|
| 1971 |
Nakanishi K, Schooley DA, Koreeda M, Dillon J. Absolute configuration of the C18 juvenile hormone: Application of a new circular dichroism method using tris(dipivaloylmethanato)praseodymium Journal of the Chemical Society D: Chemical Communications. 1235-1236. DOI: 10.1039/C29710001235 |
0.399 |
|
| 1971 |
KOREEDA M, SCHOOLEY DA, NAKANISHI K, HAGIWARA H. ChemInform Abstract: ABSOLUTE KONFIGURATION AN C-20 UND C-22 IN ECDYSONEN Chemischer Informationsdienst. Organische Chemie. 2. DOI: 10.1002/Chin.197144088 |
0.427 |
|
| 1971 |
IMAI S, MURATA E, FUJIOKA S, MATSUOKA T, KOREEDA M, NAKANISHI K, GOTO M. ChemInform Abstract: INSEKTENHORMONE 19. MITT. STRUKTUREN VON STACHYSTERON A, DEM ERSTEN NATUERLICHEN C27-STEROID MIT EINER UMGELAGERTEN METHYLGRUPPE UND VON STACHYSTERON B 20. MITT. AJUGALACTON, EIN INSEKTENHAEUTUNGSINHIBITOR (GEPRUEFT DURCH DIE CHILO-′D Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197109393 |
0.342 |
|
| 1970 |
Imai S, Murata E, Fujioka S, Matsuoka T, Koreeda M, Nakanishi K. Structures of stachysterones C and D Journal of the Chemical Society D: Chemical Communications. 352-353. DOI: 10.1039/C29700000352 |
0.318 |
|
| 1970 |
Koreeda M, Nakanishi K. 5β-Hydroxy-ecdysones and a revision of the structure of ponasterone C Journal of the Chemical Society D: Chemical Communications. 351-352. DOI: 10.1039/C29700000351 |
0.446 |
|
| 1970 |
Nakanishi K, Koreeda M, Goto M. Insect hormones. XX. Ajugalactone, an insect-molting inhibitor, as tested by the Chilo dipping method Journal of the American Chemical Society. 92: 7512-7513. DOI: 10.1021/Ja00728A068 |
0.37 |
|
| 1970 |
Nakanishi K, Imai S, Murata E, Fujioke S, Matsuoka T, Koreeda M. Insect hormones. XIX. Structures of stachysterone A, the first natural 27-carbon steroid with a rearranged methyl group, and stachysterone B Journal of the American Chemical Society. 92: 7510-7512. DOI: 10.1021/Ja00728A067 |
0.428 |
|
| 1970 |
IMAI S, MURATA E, FUJIOKA S, MATSUOKA T, KOREEDA M, NAKANISHI K. ChemInform Abstract: KONSTIT. DES STACHYSTERON C UND D Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197028413 |
0.339 |
|
| 1969 |
Koreeda M, Harada N, Nakanishi K. Interaction between non-adjacent benzoate groups: An extension of the dibenzoate chirality rule Journal of the Chemical Society D: Chemical Communications. 548-549. DOI: 10.1039/C29690000548 |
0.364 |
|
| 1969 |
Imai S, Murata E, Fujioka S, Koreeda M, Nakanishi K. Structure of ajugasterone C, a phytoecdysone with an 11-hydroxy-group Journal of the Chemical Society D: Chemical Communications. 546-547. DOI: 10.1039/C29690000546 |
0.334 |
|
| 1967 |
Kobayashi M, Nakanishi K, Koreeda M. The moulting hormone activity of ponasterones on Musca domestica (Diptera) and Bombyx mori (Lepidoptera). Steroids. 9: 529-36. PMID 6038702 DOI: 10.1016/0039-128X(67)90106-7 |
0.308 |
|
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