| Year |
Citation |
Score |
| 2003 |
Ziegler FE, Sarpong MA. Radical cyclization studies directed toward the synthesis of BMS-200475 'entecavir': The carbocyclic core Tetrahedron. 59: 9013-9018. DOI: 10.1016/J.Tet.2003.02.001 |
0.713 |
|
| 2003 |
Ziegler FE, Fowler KW, Rodgers WB, Wester RT. Ambient-Temperature Ullman Reaction: 4,5,4′,5′-Tetramethoxy-1,1′-Biphenyl-2,2′-Dicarboxaldehyde Organic Syntheses. 108-108. DOI: 10.1002/0471264180.Os065.15 |
0.345 |
|
| 2003 |
Wender PA, Eissenstat MA, Sapuppo N, Ziegler FE. Nitriles from Ketones: Cyclohexanecarbonitrile Organic Syntheses. 101-101. DOI: 10.1002/0471264180.Os058.18 |
0.64 |
|
| 2000 |
Ziegler FE, Berlin MY, Lee K, Looker AR. Formation of 9,10-unsaturation in the mitomycins: facile fragmentation of beta-alkyl-beta-aryl-alpha-oxo-gamma-butyrolactones. Organic Letters. 2: 3619-21. PMID 11073659 DOI: 10.1021/Ol000245G |
0.724 |
|
| 2000 |
Ziegler FE, Kover RX, Yee NNK. Studies directed toward the synthesis of FS-2: Observations on the fragmentation of cyclobutylcarbinyl radicals Tetrahedron Letters. 41: 5155-5159. DOI: 10.1016/S0040-4039(00)00810-8 |
0.386 |
|
| 1998 |
Ziegler FE, Wang Y. A Synthesis of (+)-Cyclophellitol from D-Xylose. The Journal of Organic Chemistry. 63: 426-427. PMID 11672025 DOI: 10.1021/Jo971998S |
0.319 |
|
| 1998 |
Ziegler FE, Wang Y. Free Radical Studies and Solutions to the Synthesis of (+)-Cyclophellitol Journal of Organic Chemistry. 63: 7920-7930. DOI: 10.1021/Jo981211D |
0.428 |
|
| 1998 |
Ziegler FE, Berlin MY. A synthesis of (+)-9a-desmethoxymitomycin A via aziridinyl radical cyclization Tetrahedron Letters. 39: 2455-2458. DOI: 10.1016/S0040-4039(98)00286-X |
0.48 |
|
| 1996 |
Ziegler FE, Wang Y. Carbon-carbon bond forming reactions with oxiranyl radicals Tetrahedron Letters. 37: 6299-6302. DOI: 10.1016/0040-4039(96)01384-6 |
0.345 |
|
| 1996 |
Ziegler FE, Petersen AK. Tandem cyclopropylcarbinyl/oxiranylcarbinyl radical rearrangements: An entry into the prostaglandin B1 series Tetrahedron Letters. 37: 809-812. DOI: 10.1016/0040-4039(95)02327-5 |
0.355 |
|
| 1995 |
Ziegler FE, Harran PG. A Synthesis of Naturally Occurring (1S,2S,3R)-4-Hydroxymethylcyclopent-4-ene-1,2,3-triol Utilizing the Cyclization of a Dioxolanyl Radical Synlett. 1995: 493-494. DOI: 10.1055/S-1995-5262 |
0.736 |
|
| 1995 |
Ziegler FE, Wallace OB. The Total Synthesis of (.+-.)-Scopadulcic Acids A and B and (.+-.)-Scopadulciol The Journal of Organic Chemistry. 60: 3626-3636. DOI: 10.1021/Jo00117A011 |
0.328 |
|
| 1995 |
Ziegler FE, Petersen AK. Allyloxy radicals are formed reversibly from oxiranylcarbinyl radicals: A kinetic study Journal of Organic Chemistry. 60: 2666-2667. DOI: 10.1021/Jo00114A011 |
0.302 |
|
| 1994 |
Ziegler FE, Belema M. Cyclization of chiral carbon-centered aziridinyl radicals: A new route to azirino[2′,3′:3,4]pyrrolo[1,2-a]indoles Journal of Organic Chemistry. 59: 7962-7967. DOI: 10.1021/Jo00105A009 |
0.368 |
|
| 1994 |
Ziegler FE, Petersen AK. Tandem fragmentation of cyclopropylcarbinyl/oxiranylcarbinyl radicals. On the reversibility of oxiranylcarbinyl/allyloxyl radical formation Journal of Organic Chemistry. 59: 2707-2714. DOI: 10.1021/Jo00089A012 |
0.351 |
|
| 1994 |
Ziegler FE, Kim H. A selective Baeyer-Villiger oxidation: a total synthesis of (-)acetomycin Tetrahedron Letters. 35: 968. DOI: 10.1016/S0040-4039(00)61535-6 |
0.386 |
|
| 1993 |
Ziegler FE, Harran PG. Intramolecular addition of a dioxolanyl radical to the indole nucleus: Preparation of enantiomerically pure, oxygenated perhydro-3H-pyrrolo[1,2-a]indoles Journal of Organic Chemistry. 58: 2768-2773. DOI: 10.1021/Jo00062A019 |
0.764 |
|
| 1993 |
Ziegler FE, Metcalf CA, Nangia A, Schulte G. Structure and total Synthesis of sporol and neosporol Journal of the American Chemical Society. 115: 2581-2589. DOI: 10.1021/Ja00060A006 |
0.538 |
|
| 1993 |
Ziegler FE, Harran PG. A route to chiral epoxypyrroloindoles via oxiranyl radical cyclization Tetrahedron Letters. 34: 4505-4508. DOI: 10.1016/0040-4039(93)88070-Y |
0.754 |
|
| 1992 |
Ziegler FE, Metcalf CA, Schulte G. Confirmation by total synthesis of the revised structure of sporol: an application of cyclic thionocarbonate-initiated radical cyclization Tetrahedron Letters. 33: 3117-3120. DOI: 10.1016/S0040-4039(00)79828-5 |
0.439 |
|
| 1991 |
Ziegler FE, Jeroncic LO. A new route to 9,9a-dihydro-3H-pyrrolo[1,2-a]indoles via radical cyclization Journal of Organic Chemistry. 56: 3479-3486. DOI: 10.1021/Jo00011A008 |
0.431 |
|
| 1990 |
Ziegler FE, Becker MR. Total synthesis of (-)-denticulatins A and B: Marine polypropionates from Siphonaria denticulata Journal of Organic Chemistry. 55: 2800-2805. DOI: 10.1021/Jo00296A044 |
0.428 |
|
| 1990 |
Ziegler FE, Sobolov SB. Synthesis of a highly functionalized carbon ring skeleton for the trichothecene anguidine Journal of the American Chemical Society. 112: 2749-2758. DOI: 10.1021/Ja00163A043 |
0.336 |
|
| 1989 |
Ziegler FE, Cain WT. Formal synthesis of (-)-calcimycin (A-23187) via the 3-methyl-.gamma.-butyrolactone approach Journal of Organic Chemistry. 54: 3347-3353. DOI: 10.1021/Jo00275A019 |
0.341 |
|
| 1988 |
Ziegler FE, Cain WT, Kneisley A, Stirchak EP, Wester RT. Applications of the 3-methyl-γ-butyrolactone strategy to the synthesis of polypropionates: The prelog-djerassi lactonic ester, ent-invictolide, and the C19-C27 fragment of rifamycin S Journal of the American Chemical Society. 110: 5442-5452. DOI: 10.1021/Ja00224A032 |
0.367 |
|
| 1988 |
Ziegler FE, Kneisley A, Thottathil JK, Wester RT. 3-Methyl-.gamma.-butyrolactones as templates for the synthesis of polypropionates: the basic strategy Journal of the American Chemical Society. 110: 5434-5442. DOI: 10.1021/Ja00224A031 |
0.385 |
|
| 1988 |
Ziegler FE, Nangia A, Schulte G. The synthesis of neosporol: A trichothecene in search of a natural product Tetrahedron Letters. 29: 1669-1672. DOI: 10.1016/S0040-4039(00)82013-4 |
0.591 |
|
| 1988 |
Ziegler FE, Nangia A, Tempesta MS. Sporol: A structure revision Tetrahedron Letters. 29: 1665-1668. DOI: 10.1016/S0040-4039(00)82012-2 |
0.445 |
|
| 1987 |
Ziegler FE, Jaynes BH, Saindane MT. A synthetic route to forskolin Journal of the American Chemical Society. 109: 8115-8116. DOI: 10.1021/Ja00260A044 |
0.319 |
|
| 1987 |
Ziegler FE, Nangia A, Schulte G. Synthesis of the 1,3-dioxolane ring system of the trichothecenes sambucinol and sporol via a stereoselective Claisen rearrangement Journal of the American Chemical Society. 109: 3987-3991. DOI: 10.1021/Ja00247A026 |
0.575 |
|
| 1987 |
Ziegler FE, Zheng Zl. Functionalized cyclopentanes via radical cyclizations using thiocarbonate derivatives as initiators and terminators Tetrahedron Letters. 28: 5973-5976. DOI: 10.1016/S0040-4039(00)96840-0 |
0.425 |
|
| 1987 |
Ziegler FE, Jaynes BH. Reconstitution of forskolin from a ring C dihydropyran-4-one degradation product thereof Tetrahedron Letters. 28: 2339-2342. DOI: 10.1016/S0040-4039(00)96118-5 |
0.363 |
|
| 1987 |
Ziegler FE, Kneisley A. 3-Methyl-γ-butyrolactone as a source of 2-methyl-3-hydroxyketones and 2-methyl-1,3-diols: a synthesis of the C19C27 fragment of rifamycin S by linear iteration Tetrahedron Letters. 28: 1725-1728. DOI: 10.1016/S0040-4039(00)95405-4 |
0.379 |
|
| 1986 |
Ziegler FE, Hwang KJ, Kadow JF, Klein SI, Pati UK, Wang TF. Practical routes to two functionalized decalones for the synthesis of quassinoids Journal of Organic Chemistry. 51: 4573-4579. DOI: 10.1021/Jo00374A016 |
0.33 |
|
| 1986 |
Ziegler FE, Stirchak EP, Wester RT. R-3-methyl-γ-butyrolactone as a template for the synthesis of (+)-invictolide Tetrahedron Letters. 27: 1229-1232. DOI: 10.1016/S0040-4039(00)84224-0 |
0.386 |
|
| 1986 |
Ziegler FE, Wester RT. Regiochemical control in the hemiacetalization of a dihydroxydialdehyde. An application of the use of homochiral 3-methyl-δ-butyrolactones to the construction of homochiral tripropionate units. Tetrahedron Letters. 27: 1225-1228. DOI: 10.1016/S0040-4039(00)84223-9 |
0.328 |
|
| 1986 |
Ziegler FE, Kneisley A, Wester RT. On the extent of racemization of allylic esters during palladium-mediated alkylation with homochiral 3-methyl-δ-butyrolactone derivatives Tetrahedron Letters. 27: 1221-1224. DOI: 10.1016/S0040-4039(00)84222-7 |
0.373 |
|
| 1986 |
ZIEGLER FE, JAYNES BH. ChemInform Abstract: Rearrangement of a Hindered Allylic Alcohol During Vanadium-Catalyzed Epoxidation. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198615194 |
0.312 |
|
| 1985 |
Ziegler FE, Kneisley A. A contrathermodynamic epimerization of a 2,3-trans-disubstituted butyrolactone: intermediates for chiral polypropionate units. Tetrahedron Letters. 26: 263-266. DOI: 10.1016/S0040-4039(01)80792-9 |
0.352 |
|
| 1985 |
Ziegler FE, Jaynes BE, Saindane MT. A C6, C7 Oxygen Functionalized Intermediate for the Synthesis of Forskolin: Stereochemical Control in an Intramolecular Diels-Alder Reaction Tetrahedron Letters. 26: 3307-3310. DOI: 10.1016/S0040-4039(00)98284-4 |
0.404 |
|
| 1985 |
Ziegler FE, Jaynes BH. Rearrangement of a hindered allylic alcohol during vanadium-catalyzed epoxidation. A short synthesis of uvidin-c. Tetrahedron Letters. 26: 5875-5878. DOI: 10.1016/S0040-4039(00)98250-9 |
0.353 |
|
| 1985 |
Ziegler FE, Wang TF. On the mechanism of the mander carbomethoxylation of ketone enolates with methyl cyanoformate Tetrahedron Letters. 26: 2291-2292. DOI: 10.1016/S0040-4039(00)95077-9 |
0.37 |
|
| 1985 |
Ziegler FE, Klein SI, Pati UK, Wang TF. Acyclic diastereoselection as a synthetic route to quassinoids: A Claisen rearrangement based strategy for bruceantin Journal of the American Chemical Society. 107: 2730-2737. DOI: 10.1002/Chin.198536332 |
0.344 |
|
| 1984 |
Ziegler FE, Wang TF. Synthesis of (±)-11-ketoprogesterone, a precursor to the corticosteroids. An improved method for the introduction of the carbon 19 methyl group into A-ring aromatic steroids Journal of the American Chemical Society. 106: 718-721. DOI: 10.1021/Ja00315A043 |
0.344 |
|
| 1984 |
Ziegler FE, Wester RT. Acyclic stereocontrol via the claisen rearrangement: a formal synthesis of (+) tirandamycic acid Tetrahedron Letters. 25: 617-620. DOI: 10.1016/S0040-4039(00)99953-2 |
0.406 |
|
| 1984 |
Ziegler FE, Mikami K. Alkylation of 1-trimethylsilylvinyl aluminates with "unreactive" alkyl halides mediated by cuprous iodide-trimethyl phosphite complex Tetrahedron Letters. 25: 131-134. DOI: 10.1016/S0040-4039(00)99821-6 |
0.339 |
|
| 1984 |
Ziegler FE, Mikami K. The effect of the trimethylsilyl group on the regiochemistry of the ene reaction Tetrahedron Letters. 25: 127-130. DOI: 10.1016/S0040-4039(00)99820-4 |
0.337 |
|
| 1984 |
Ziegler FE, Mencel JJ. The tandem claisen-ene rearrangement: a method for the stereocontrolled synthesis of functionalized cyclopentanoids Tetrahedron Letters. 25: 123-126. DOI: 10.1016/S0040-4039(00)99819-8 |
0.398 |
|
| 1984 |
Ziegler FE, Lim H. Tandem Cope-Claisen rearrangement in the synthesis of steroids: Stork's keto acid Journal of Organic Chemistry. 49: 3278-3281. DOI: 10.1002/Chin.198511247 |
0.375 |
|
| 1984 |
Ziegler FE, Wang T-. Synthesis Of (.+-.)-11-Ketoprogesterone, A Precursor To The Corticosteroids. An Improved Method For The Introduction Of The Carbon 19 Methyl Group Into A-Ring Aromatic Steroids Cheminform. 15. DOI: 10.1002/Chin.198419313 |
0.366 |
|
| 1984 |
ZIEGLER FE, MENCEL JJ, MIKAMI K. ChemInform Abstract: The Tandem Claisen-Ene Rearrangement: A Method for the Stereocontrolled Synthesis of Functionalized Cyclopentanoids. The Effect of the Trimethylsilyl Group on the Regiochemistry of the Ene Reaction. Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198419154 |
0.374 |
|
| 1983 |
Ziegler FE, Mencel JJ. Application of dithianylidene anions to the synthesis of de-ab-8-carbomethoxycholestan-9-one: a steroid and vitamin D synthon Tetrahedron Letters. 24: 1859-1862. DOI: 10.1016/S0040-4039(00)81790-6 |
0.355 |
|
| 1983 |
Ziegler FE, Hwang KJ. On the aprotic Robinson annelation of dihydrocarvone and 2-methylcyclohexanone with methyl and ethyl vinyl ketone Journal of Organic Chemistry. 48: 3349-3351. DOI: 10.1002/Chin.198407178 |
0.357 |
|
| 1982 |
Ziegler FE, Lim H. A synthesis of (.+-.)-estrone methyl ether via the tandem Cope-Claisen rearrangement Journal of Organic Chemistry. 14: 5229-5230. DOI: 10.1021/Jo00147A046 |
0.422 |
|
| 1982 |
Ziegler FE, Piwinski JJ. Tandem Cope-Claisen rearrangement: Scope and stereochemistry Journal of the American Chemical Society. 104: 7181-7190. DOI: 10.1021/Ja00389A048 |
0.349 |
|
| 1982 |
Ziegler FE, Fang JM, Tam CC. Conjugate addition of dithianylidene anions to α,β-unsaturated ketones. An application to the total synthesis of (±)-aromatin and (±)-confertin Journal of the American Chemical Society. 104: 7174-7181. DOI: 10.1021/Ja00389A047 |
0.315 |
|
| 1982 |
Ziegler FE, Thottathil JK. High diastereoselection in the claisen rearrangement of enantiomerically pure butyrolactones Tetrahedron Letters. 23: 3531-3534. DOI: 10.1016/S0040-4039(00)87661-3 |
0.304 |
|
| 1981 |
Ziegler FE, Gilligan PJ. Synthetic studies on the carbomycins (magnamycins): An exception to the enantioselective synthesis of β-alkyl carboxylic acids via chiral oxazolines Journal of Organic Chemistry. 46: 3874-3880. DOI: 10.1021/Jo00332A023 |
0.397 |
|
| 1981 |
Ziegler FE, Thottathil JK. A facile construction of the 2,9-dioxabicyclo-[3.3.1]- non-7-en-6-one ring system: A model for tirandanycin. Tetrahedron Letters. 22: 4883-4886. DOI: 10.1016/S0040-4039(01)92371-8 |
0.306 |
|
| 1981 |
Ziegler FE, Wang TF. A formal, stereocontrolled synthesis of (±) estrone employing the trimethylsilylcyanohydrin cope rearrangement Tetrahedron Letters. 22: 1179-1182. DOI: 10.1016/S0040-4039(01)90268-0 |
0.341 |
|
| 1981 |
Ziegler FE, Chakraborty UR, Weisenfeld RB. A palladium-catalyzed carbon-carbon bond formation of conjugated dienones. A macrocyclic dienone lactone model for the carbomycins Tetrahedron. 37: 4035-4040. DOI: 10.1016/S0040-4020(01)93278-8 |
0.355 |
|
| 1980 |
Ziegler FE, Guenther T, Nelson RV. Monoalkylidene Derivatives Of Meldrum's Acid Synthetic Communications. 10: 661-665. DOI: 10.1080/00397918008065647 |
0.311 |
|
| 1980 |
Ziegler FE, Piwinski JJ. Stereochemical course of the Cope-Claisen rearrangement of the stereoisomeric 2-vinyl-3-isopropenylcyclohexylvinyl ethers. A system having .DELTA.GClaisen.++. .mchgt. .DELTA.GCope.++. Journal of the American Chemical Society. 102: 880-882. DOI: 10.1021/Ja00522A091 |
0.332 |
|
| 1980 |
Ziegler FE, Chliwner I, Fowler KW, Kanfer SJ, Kuo SJ, Sinha ND. The ambient temperature Ullmann reaction and its application to the total synthesis of (±)-steganacin Journal of the American Chemical Society. 102: 790-798. DOI: 10.1021/Ja00522A058 |
0.313 |
|
| 1980 |
Ziegler FE, Nelson RV, Wang Tf. A homologous ester claisen rearrangement via the cope rearrangement of O-trimethylsilylcyanohydrins Tetrahedron Letters. 21: 2125-2128. DOI: 10.1016/S0040-4039(00)78975-1 |
0.329 |
|
| 1979 |
Ziegler FE, Chan Tam C. Ketene dithioacetals III: the conjugate addition of ketene dithioacetal anions to cyclic α,β-unsaturated ketones Tetrahedron Letters. 20: 4717-4720. DOI: 10.1016/S0040-4039(01)86692-2 |
0.327 |
|
| 1979 |
Ziegler FE, Cady MA, Nelson RV, Photis JM. A novel 2,3-dioxo-norcar-4-ene-7-carboxylic acid via rearrangement of an α-diketone Tetrahedron Letters. 20: 2741-2744. DOI: 10.1016/S0040-4039(01)86403-0 |
0.356 |
|
| 1978 |
Ziegler FE, Schwartz JA. Synthetic studies on lignan lactones: aryl dithiane route to (.+-.)-podorhizol and (.+-.)-isopodophyllotoxone and approaches to the stegane skeleton Journal of Organic Chemistry. 43: 985-991. DOI: 10.1021/Jo00399A040 |
0.33 |
|
| 1978 |
Ziegler FE, Fowler KW, Sinha ND. A total synthesis of (±) steganacin via the modified Ullmann reaction Tetrahedron Letters. 19: 2767-2770. DOI: 10.1016/S0040-4039(01)94857-9 |
0.333 |
|
| 1977 |
Ziegler FE, Wender PA. Methyldialkylcyanodiazenecarboxylates as intermediates for transforming aliphatic ketones into nitriles The Journal of Organic Chemistry. 42: 2001-2003. DOI: 10.1021/Jo00431A036 |
0.592 |
|
| 1977 |
Ziegler FE, Reid GR, Studt WL, Wender PA. Stereochemistry of dialkylcuprate additions to cyclopropyl acrylic esters. An application to the synthesis of (.+-.)-eremophilone The Journal of Organic Chemistry. 42: 1991-2001. DOI: 10.1021/Jo00431A035 |
0.658 |
|
| 1977 |
Ziegler FE. Stereo- and regiochemistry of the claisen rearrangement: Applications to natural products synthesis Accounts of Chemical Research. 10: 227-232. DOI: 10.1021/Ar50114A006 |
0.366 |
|
| 1977 |
Ziegler FE, Kloek JA. The stereocontrolled photoaddition of allene to cyclopent-1-ene-1-carboxaldehydes. A total synthesis of (±) steviol methyl ester and isosteviol methyl ester Tetrahedron. 33: 373-380. DOI: 10.1016/0040-4020(77)80089-6 |
0.382 |
|
| 1975 |
Ziegler FE, Schwartz JA. The alkylation and aldolization of lactone enolates derived by the conjugate addition of an aryl dithiane anion to 2-butenolide: A synthesis of (±)podorhizol and (±)epipodorhizol. Tetrahedron Letters. 16: 4643-4646. DOI: 10.1016/S0040-4039(00)91041-4 |
0.339 |
|
| 1974 |
Ziegler FE, Wender PA. The stereospecific generation of the cis-vicinal methyls in eremophilane and valencane sesquiterpenes: The total synthesis of (±) eremophilone and (±) 7-epieremophilone. Tetrahedron Letters. 15: 449-452. DOI: 10.1016/S0040-4039(01)82239-5 |
0.588 |
|
| 1974 |
Ziegler FE, Kloek JA. The stereochemistry of the photoaddition of allene to cyclopent-1-ene-1-carboxaldehydes Tetrahedron Letters. 15: 315-318. DOI: 10.1016/S0040-4039(01)82203-6 |
0.36 |
|
| 1974 |
Ziegler FE, Bennett GB. The Claisen Rearrangement In Indole Alkaloid Synthesis, The Total Synthesis Of (+-)-Tabersonine Cheminform. 5. DOI: 10.1002/Chin.197402426 |
0.425 |
|
| 1973 |
Ziegler FE, Spitzner EB. A biogenetically modeled synthesis via an indole acrylic ester. A total synthesis of (±)-minovine Journal of the American Chemical Society. 95: 7146-7149. PMID 4784289 DOI: 10.1021/Ja00802A040 |
0.375 |
|
| 1973 |
Ziegler FE, Bennett GB. The claisen rearrangement in indole alkaloid synthesis. The total synthesis of ( )-tabersonine. Journal of the American Chemical Society. 95: 7458-64. PMID 4747879 DOI: 10.1021/Ja00803A041 |
0.425 |
|
| 1973 |
Ziegler FE, Spitzner EB. A Biogenetically Modeled Synthesis Via An Indole Acrylic Ester, A Total Synthesis Of (+-)-Minovine Cheminform. 4. DOI: 10.1002/Chin.197352486 |
0.362 |
|
| 1971 |
Ziegler FE, Condon ME. Gibbane synthons via hexahydrofluorenones. An intramolecular reformatsky reaction Journal of Organic Chemistry. 36: 3707-3714. DOI: 10.1021/Jo00823A010 |
0.307 |
|
| 1971 |
Ziegler FE, Bennett GB. Total synthesis of (+-)-tabersonine Journal of the American Chemical Society. 93: 5930-5931. DOI: 10.1021/Ja00751A076 |
0.392 |
|
| 1971 |
Ziegler FE, Wender PA. Base-induced decomposition of methyl dialkylcyanodiazenecarboxylates. Transformation of ketones into nitriles, .alpha.-carbomethoxynitriles, and .alpha.-methylnitriles Journal of the American Chemical Society. 93: 4318-4319. DOI: 10.1021/Ja00746A052 |
0.589 |
|
| 1971 |
ZIEGLER FE, WENDER PA. ChemInform Abstract: BASENINDUZIERTE ZERS. VON DIALKYLCYANDIAZENCARBONSAEUREMETHYLESTERN, UMWANDLUNG VON KETONEN IN NITRILE, ALPHA-METHOXYCARBONYL- UND ALPHA-METHYL-NITRILE Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197145280 |
0.582 |
|
| 1970 |
Ziegler FE, Spitzner EB. The biogenetically modeled total synthesis of (plus minus)-minovine. Journal of the American Chemical Society. 92: 3492-4. PMID 5422770 DOI: 10.1021/Ja00714A058 |
0.332 |
|
| 1970 |
Ziegler FE, Bennett GB. The synthesis of 6,7-dehydroquebrachamine Tetrahedron Letters. 11: 2545-2547. DOI: 10.1016/S0040-4039(01)98277-2 |
0.405 |
|
| 1969 |
Ziegler F, Kloek J, Zoretic P. Additions and Corrections - A Synthesis of Quebrachamine and 3,4-Dehydroquebrachamine Journal of the American Chemical Society. 91: 4943-4943. DOI: 10.1021/Ja01045A606 |
0.373 |
|
| 1969 |
Ziegler FE, Kloek JA, Zoretic PA. A synthesis of quebrachamine and 3,4-dehydroquebrachamine Journal of the American Chemical Society. 91: 2342-2350. DOI: 10.1021/Ja01037A026 |
0.405 |
|
| 1969 |
Ziegler FE, Sweeny JG. A synthesis of dihydrocorynantheol and 3-epi-dihydrocorynantheol Tetrahedron Letters. 10: 1097-1100. DOI: 10.1016/S0040-4039(01)97749-4 |
0.407 |
|
| 1969 |
Ziegler FE, Condon ME. A facile route to -hexahydrofluoren-2,9-dione and its 7-methoxy analog. Tetrahedron Letters. 10: 2315-2317. DOI: 10.1016/S0040-4039(01)88151-X |
0.338 |
|
| 1968 |
Ziegler FE, Zoretic PA. The alkylation of cyclic enamines: a synthesis of the quebrachamine skeleton Tetrahedron Letters. 9: 2639-2641. DOI: 10.1016/S0040-4039(00)89662-8 |
0.454 |
|
| 1966 |
Büchi G, Coffen DL, Kocsis K, Sonnet PE, Ziegler FE. The total synthesis of iboga alkaloids Journal of the American Chemical Society. 88: 3099-3109. DOI: 10.1021/Ja00965A039 |
0.401 |
|
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