| Year |
Citation |
Score |
| 1985 |
Wiesner K. Some Highlights In The Structural And Synthetic Chemistry Of The Aconite Alkaloids Tetrahedron. 41: 485-497. DOI: 10.1016/S0040-4020(01)96490-7 |
0.375 |
|
| 1985 |
Wiesner K, Tsai TYR, Jin H. On Cardioactive Steroids. XVI. Stereoselective β-Glycosylation of Digitoxose: The Synthesis of Digitoxin† Helvetica Chimica Acta. 68: 300-314. DOI: 10.1002/Hlca.19850680203 |
0.344 |
|
| 1985 |
Wiesner K, Tsai TYR, Jin H. ON CARDIOACTIVE STEROIDS. XVI. STEREOSELECTIVE β-GLYCOSYLATION OF DIGITOXOSE: THE SYNTHESIS OF DIGITOXIN Cheminform. 16. DOI: 10.1002/Chin.198526335 |
0.34 |
|
| 1984 |
Tsai TYR, Jin H, Wiesner K. A stereoselective synthesis of digitoxin. On cardioactive steroids. XIII Canadian Journal of Chemistry. 62: 1403-1405. DOI: 10.1139/V84-238 |
0.457 |
|
| 1984 |
Wiesner K, Tsai TYR, Kumar R, Sivaramakrishnan H. On cardioactive steroids. Communication XV. A stereoselective synthesis of (21R)-21-methyldigitoxigenin, a fully active cardenolide with a wide margin of safety: A contribution to the topology of theDigitalis receptors Helvetica Chimica Acta. 67: 1128-1135. DOI: 10.1002/Hlca.19840670427 |
0.334 |
|
| 1984 |
WIESNER K, TSAI TYR, SEN A, KUMAR R, TSUBUKI M. ChemInform Abstract: ON CARDIOACTIVE STEROIDS. XII. THE SYNTHESIS OF (NATURAL) BUFALIN AND α′-ISOBUFALIN Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198411330 |
0.469 |
|
| 1984 |
Jin H, Tsai TYR, Wiesner K. On The Synthesis Of Cardioactive Steroid Glycosides. On Cardioactive Steroids. I Cheminform. 15. DOI: 10.1002/Chin.198403330 |
0.466 |
|
| 1983 |
Wiesner K, Tsai TYR, Sen A, Kumar R, Tsubuki M. On cardioactive steroids. XII. The synthesis of (natural) bufalin and α′‐isobufalin Helvetica Chimica Acta. 66: 2632-2640. DOI: 10.1002/Hlca.19830660831 |
0.474 |
|
| 1982 |
Tsai TYR, Wiesner K. On cardioactive steroids. IX. The conversion of digitoxigenin to bufalin Canadian Journal of Chemistry. 60: 2161-2163. DOI: 10.1139/V82-309 |
0.38 |
|
| 1982 |
Sen A, Jäggi FJ, Tsai TYR, Wiesner K. A simple and efficient synthesis of bufalin Journal of the Chemical Society, Chemical Communications. 1213-1214. DOI: 10.1039/C39820001213 |
0.407 |
|
| 1982 |
Wiesner K, Tsai TYR, Jäggi FJ, Tsai CSJ, Gray GD. On Cardioactive Steroids. VIII. The Synthesis of Bufalin and Resibufogenin Isomers Helvetica Chimica Acta. 65: 2049-2060. DOI: 10.1002/Hlca.19820650712 |
0.323 |
|
| 1981 |
Wiesner K, Marini-Bettolo R, Tsai CSJ, Tsai TYR. A One-step Synthesis of 17a-Hydroxy Cardenolides and lsocardenolides from C17 Steroidal Ketones Heterocycles. 15: 305. DOI: 10.3987/S-1981-01-0305 |
0.35 |
|
| 1981 |
Marini-Bettolo R, Flecker P, Tsai TYR, Wiesner K. On cardioactive steroids. IV. A new synthesis of cardenolides Canadian Journal of Chemistry. 59: 1403-1404. DOI: 10.1139/V81-206 |
0.468 |
|
| 1981 |
Wiesner K, Shiao M, Tsai TYR. On Cardioactive Steroids V. Synthesis of the Pyridone Analogue of Bufalin Cheminform. 13: 1879. DOI: 10.1002/Chin.198216313 |
0.404 |
|
| 1981 |
Marini-Bettolo R, Flecker P, Tsai TYR, Wiesner K. On Cardioactive Steroids. Iv. A New Synthesis Of Cardenolides Cheminform. 12. DOI: 10.1002/Chin.198136333 |
0.448 |
|
| 1981 |
Sethi SP, Atwal KS, Marini-Bettolo RM, Tsai TYR, Wiesner K. A Stereospecific Synthesis Of Napelline Cheminform. 12. DOI: 10.1002/Chin.198104332 |
0.495 |
|
| 1980 |
Wiesner K, Sethi SP, Sterzycki R, Sy WW, Martini-Bettolo R, Tsai TYR. The Total Synthesis of Diacetyloxodenudatine Heterocycles. 14: 23. DOI: 10.3987/R-1980-01-0023 |
0.476 |
|
| 1980 |
Sethi SP, Atwal KS, Marini-Bettolo RM, Tsai TYR, Wiesner K. A stereospecific synthesis of napelline Canadian Journal of Chemistry. 58: 1889-1891. DOI: 10.1139/V80-298 |
0.479 |
|
| 1979 |
Tsai TYR, Nambiar KP, Krikorian D, Botta M, Marini-Bettolo R, Wiesner K. A new synthesis of chasmanine and 13-desoxydelphonine: a preferred route to the aromatic intermediate Canadian Journal of Chemistry. 57: 2124-2134. DOI: 10.1139/V79-341 |
0.432 |
|
| 1979 |
Wiesner K, Tsai TYR, Minta A. A Simple Synthesis Of Cardenolides And Their Less Toxic Isomers Via Furyl Intermediates Cheminform. 11: 1397. DOI: 10.1002/Chin.198015338 |
0.452 |
|
| 1979 |
TSAI TYR, NAMBIAR KP, KRIKORIAN D, BOTTA M, MARINI-BETTOLO R, WIESNER K. ChemInform Abstract: A NEW SYNTHESIS OF CHASMANINE AND 13-DESOXYDELPHONINE: A PREFERRED ROUTE TO THE AROMATIC INTERMEDIATE Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197950336 |
0.44 |
|
| 1978 |
Wiesner K, Tsai TYR, Nambiar KP. A new stereospecific total synthesis of chasmanine and 13-desoxydelphonine Canadian Journal of Chemistry. 56: 1451-1454. DOI: 10.1139/V78-237 |
0.46 |
|
| 1978 |
Atwal KS, Marini-Bettolo R, Sanchez IH, Tsai TYR, Wiesner K. On the construction of the C/D ring systems of chasmanine and napelline by diene addition Canadian Journal of Chemistry. 56: 1102-1113. DOI: 10.1139/V78-187 |
0.399 |
|
| 1977 |
Wiesner K, Tsai TYR, Tsai CSJ, Sy WW, Shanbhag MN, Liu WC, Lee SF. A Stereospecific Total Synthesis of Chasmanine Heterocycles. 7: 217. DOI: 10.3987/S-1977-01-0217 |
0.479 |
|
| 1977 |
Wiesner K, Sanchez IH, Atwal KS, Lee SF. On the construction of the C,D ring system of chasmanine by the photochemical method Canadian Journal of Chemistry. 55: 1091-1099. DOI: 10.1139/V77-152 |
0.422 |
|
| 1976 |
Lee S, Sathe GM, Sy WW, Ho P, Wiesner K. The synthesis of chasmanine: aromatic intermediate Canadian Journal of Chemistry. 54: 1039-1051. DOI: 10.1139/V76-149 |
0.442 |
|
| 1976 |
Lee S, Sathe GM, Sy WW, Ho P, Wiesner K. The Synthesis Of Chasmanine- Aromatic Intermediate Cheminform. 7. DOI: 10.1002/Chin.197632346 |
0.495 |
|
| 1975 |
Wiesner K, Ho P, Liu W, Shanbhag MN. On the Construction of Delphinine-type Alkaloids via the Rearrangement of Substituted Denudatine Derivatives Canadian Journal of Chemistry. 53: 2140-2149. DOI: 10.1139/V75-298 |
0.384 |
|
| 1975 |
Wiesner K, Ho P, Liu W, Shanbhag MN. On The Construction Of Delphinine-Type Alkaloids Via The Rearrangement Of Substituted Denudatine Derivatives Cheminform. 6. DOI: 10.1002/Chin.197544387 |
0.333 |
|
| 1974 |
Wiesner K, Ho P, Tsai CSJ(, Lam Y. The Total Synthesis of Racemic Napelline Canadian Journal of Chemistry. 52: 2355-2357. DOI: 10.1139/V74-341 |
0.468 |
|
| 1974 |
Wiesner K, Ho P, Tsai CSJ(. The Total Synthesis of a Hexacyclic Relay for the Alkaloid Napelline Canadian Journal of Chemistry. 52: 2353-2355. DOI: 10.1139/V74-340 |
0.458 |
|
| 1974 |
Wiesner K, Ho P, Oida S. A Stereospecific Synthesis of the Denudatine Skeleton: Stereospecificity of the C/D Ring Construction by Diene Addition Canadian Journal of Chemistry. 52: 1042-1049. DOI: 10.1139/V74-165 |
0.468 |
|
| 1974 |
Wiesner K, Ho P, Ohtani H. A Vinylogous Wagner Rearrangement in the Benzonorbornene Series Canadian Journal of Chemistry. 52: 640-644. DOI: 10.1139/V74-098 |
0.401 |
|
| 1974 |
Wiesner K, Ho P, Tsai CSJ, Lam Y. The Total Synthesis Of Racemic Napelline Cheminform. 5. DOI: 10.1002/Chin.197437419 |
0.479 |
|
| 1974 |
Wiesner K, Ho P, Tsai CSJ. The Total Synthesis Of A Hexacyclic Relay For The Alkaloid Napelline Cheminform. 5. DOI: 10.1002/Chin.197437418 |
0.453 |
|
| 1974 |
Wiesner K, Ho P, Oida S. A Stereospecific Synthesis Of The Denudatine Skeleton, Stereospecificity Of The C/D Ring Construction By Diene Addition Cheminform. 5. DOI: 10.1002/Chin.197426468 |
0.393 |
|
| 1974 |
Wiesner K, Ho P, Ohtani H. A Vinylogous Wagner Rearrangement In The Benzonorbornene Series Cheminform. 5. DOI: 10.1002/Chin.197418119 |
0.34 |
|
| 1974 |
Wiesner K, Ho P, Chang D, Lam YK, and CSJP, Ren WY. The Synthesis Of Songorine, A Simplified Synthesis Of The Aromatic Intermediate Cheminform. 5. DOI: 10.1002/Chin.197411479 |
0.5 |
|
| 1973 |
Wiesner K, Ho P, Jain RC, Lee SF, Oida S, Philipp A. Synthesis and Rearrangement Control of Substituted Benzobicycloheptane Aziridines Canadian Journal of Chemistry. 51: 1448-1457. DOI: 10.1139/v73-219 |
0.364 |
|
| 1971 |
Wiesner K, Jay EW, Demerson JC, Kanno T, Krepinský J, Poon L, Tsai TY, Vilím A, Wu CS. The total synthesis of delphinine: a stereoselective synthesis of an advanced relay compound. Experientia. 26: 1030-3. PMID 5478617 DOI: 10.1007/Bf02114180 |
0.448 |
|
| 1971 |
Wiesner K, Mccluskey JG, Chang JK, Šmůla V. The Total Synthesis of a Thebaine Analogue and of the Corresponding "Bentley Adduct" Canadian Journal of Chemistry. 49: 1092-1098. DOI: 10.1139/v71-179 |
0.303 |
|
| 1970 |
Wiesner K, Komlossy ZI, Philipp A, Valenta Z. The total synthesis of optically active veatchine. Experientia. 26: 471. PMID 5444813 DOI: 10.1007/Bf01898446 |
0.692 |
|
| 1970 |
Wiesner K, Deljac A, Tsai T, Przybylska M. A method for the synthesis of bridged terpenoids Tetrahedron Letters. 11: 1145-1148. DOI: 10.1016/S0040-4039(01)97931-6 |
0.3 |
|
| 1970 |
Wiesner K, Jay EWK, Demerson C, Kanno T, Krepinsky J, Poon L, Tsai TYR, Vilim A, Wu CS. Totalsynthese Von Delphinin, Stereoselektive Synthese Einer Zwischenverbindung Cheminform. 1. DOI: 10.1002/Chin.197050398 |
0.405 |
|
| 1970 |
Wiesner K, Komlossy ZI, Philipp A, Valenta Z. Totalsynth. Des Optisch Aktiven Veatchins Cheminform. 1. DOI: 10.1002/Chin.197032398 |
0.642 |
|
| 1969 |
Wiesner K, Poon L, Jirkovský I, Fishman M. The total synthesis of optically active annotinine Canadian Journal of Chemistry. 47: 433-444. DOI: 10.1139/V69-063 |
0.422 |
|
| 1968 |
Wiesner K, Poon L. Synthesis in the series of Lycopodium alkaloids. 8. The total synthesis of annotinine. Tetrahedron Letters. 49: 4937-40. PMID 6062698 DOI: 10.1016/S0040-4039(01)89941-X |
0.511 |
|
| 1968 |
Wiesner K, Uyeo S, Philipp A, Valenta Z. Synthesis in the series of diterpene alkaloids. IX. A new simple synthesis of veatchine. Tetrahedron Letters. 6279-82. PMID 5701075 DOI: 10.1016/S0040-4039(00)75452-9 |
0.755 |
|
| 1968 |
Wiesner K, Philipp A, Ho P. Synthesis in the series of diterpene alkaloids 8. A stereospecific synthesis of pentacyclic intermediates with a bridge in ring B. Tetrahedron Letters. 10: 1209-14. PMID 4170721 DOI: 10.1016/S0040-4039(01)98922-1 |
0.37 |
|
| 1967 |
Dugas H, Hazenberg ME, Valenta Z, Wiesner K. Synthesis in the series of lycopodium alkaloids. VII. The synthesis of 12-epi-lycopodine. Tetrahedron Letters. 49: 4931-6. PMID 6062697 DOI: 10.1016/S0040-4039(01)89940-8 |
0.76 |
|
| 1967 |
Wiesner K, Jirkovsky I. Synthesis in the series of Lycopodium alkaloids. V. The synthesis of annotinine lactam. Tetrahedron Letters. 22: 2077-9. PMID 6044214 DOI: 10.1016/S0040-4039(00)91017-7 |
0.473 |
|
| 1967 |
Wiesner K, Jirkovský I, Fishman M, Williams CAJ. Syntheses in the series op lycopodiom alkaloids IV. A simple photochemical synthesis of an annotinine derivative Tetrahedron Letters. 8: 1523-1526. DOI: 10.1016/S0040-4039(00)90993-6 |
0.498 |
|
| 1967 |
Wiesner K, Valenta Z, Findlay JA. The structure of ryanodine Tetrahedron Letters. 8: 221-223. DOI: 10.1016/S0040-4039(00)90521-5 |
0.667 |
|
| 1967 |
Koblicová Z, Wiesner K. Syntheses in the series of lycopodium alkaloids VI. Photochemical additions of vinylogous imides and methyl methacrylate Tetrahedron Letters. 8: 2563-2566. DOI: 10.1016/S0040-4039(00)70348-0 |
0.332 |
|
| 1966 |
Wiesner K, Santroch J. Synthesis in the series of diterpene alkaloids VII. A synthesis of compounds closely related to the aromatization products of aconitine and delphinine Tetrahedron Letters. 7: 5939-5945. DOI: 10.1016/S0040-4039(00)76113-2 |
0.46 |
|
| 1966 |
Wiesner K, Philipp A. Synthesis in the series of diterpene alkaloids V. An approach to songorine Tetrahedron Letters. 7: 1467-1470. DOI: 10.1016/S0040-4039(00)75717-0 |
0.381 |
|
| 1966 |
Guthrie RW, Valenta Z, Wiesner K. Synthesis in the series of diterpene alkaloids VI. A simple synthesis of atisine Tetrahedron Letters. 7: 4645-4654. DOI: 10.1016/S0040-4039(00)70092-X |
0.759 |
|
| 1965 |
Babin DR, Bögri T, Findlay JA, Reinshagen H, Valenta Z, Wiesner K. The complete structure of ryanodine. Experientia. 21: 425-30. PMID 5870896 DOI: 10.1007/Bf02150794 |
0.663 |
|
| 1965 |
Dugas H, Ellison RA, Valenta Z, Wiesner K, Wong CM. Synthesis of Lycopodium alkaloids. II. Development of stereospecific synthetic methods. Tetrahedron Letters. 1279-86. PMID 5844743 DOI: 10.1016/S0040-4039(00)77196-6 |
0.71 |
|
| 1965 |
Böhme EH, Valenta Z, Wiesner K. Syntheses in the series of lycopodium alkaloids. 3. A novel system active in photochemical additions. Tetrahedron Letters. 2441-4. PMID 5843624 DOI: 10.1016/S0040-4039(01)84003-X |
0.699 |
|
| 1965 |
Wiesner K, Chan KK, Demerson C. Synthesis in the series of diterpene alkaloids IV. Development of synthetic methods in the series of hexacyclic alkaloids Tetrahedron Letters. 6: 2893-2897. PMID 5828475 DOI: 10.1016/S0040-4039(00)90233-8 |
0.457 |
|
| 1965 |
Guthrie RW, Philipp A, Valenta Z, Wiesner K. Synthesis in the diterpene alkaloid series. 3. A novel synthesis of a keto lactam. A photochemical approach to the C,D-ring system of atisine. Tetrahedron Letters. 2945-50. PMID 5828041 DOI: 10.1016/S0040-4039(01)89239-X |
0.735 |
|
| 1964 |
Valenta Z, Wiesner K, Wong CM. Synthesis in the diterpene alkaloid series - II. A total synthesis of the garrya alkaloids Tetrahedron Letters. 5: 2437-2442. DOI: 10.1016/S0040-4039(00)70405-9 |
0.749 |
|
| 1964 |
Anet FAL, Haq MZ, Khan NH, Ayer WA, Hayatsu R, Valverde-Lopez S, Deslongchamps P, Riess W, Ternbah M, Valenta Z, Wiesner K. The structure of lyconnotine: A novel lycopodium alkaloid Tetrahedron Letters. 5: 751-757. DOI: 10.1016/0040-4039(64)83031-8 |
0.748 |
|
| 1962 |
VALENTA Z, WIESNER K, BABIN DR, BOGRI T, FORREST TP, FRIED F, REINSHAGEN H. On the structure of ryanodol. Experientia. 18: 111-3. PMID 13924329 DOI: 10.1007/Bf02153842 |
0.642 |
|
| 1962 |
Findlay JA, Henry WA, Jain TC, Valenta Z, Wiesner K, Wong CM. Synthesis in the diterpene alkaloid series - I the stereospecific synthesis of an intermediate and its identification with a natural degradation product Tetrahedron Letters. 3: 869-872. DOI: 10.1016/S0040-4039(00)71737-0 |
0.743 |
|
| 1962 |
Wiesner K, Valenta Z, Humber LG. On the hofmann degradation of hetisine Tetrahedron Letters. 3: 621-625. DOI: 10.1016/S0040-4039(00)70919-1 |
0.642 |
|
| 1961 |
Wiesner K, Francis JE, Findlay JA, Valenta Z. The configuration of annotinine and some rearrangements Tetrahedron Letters. 2: 187-196. DOI: 10.1016/S0040-4039(01)84063-6 |
0.674 |
|
| 1958 |
WIESNER K, VALENTA Z. Recent progress in the chemistry of the aconitegarrya alkaloids. Fortschritte Der Chemie Organischer Naturstoffe = Progress in the Chemistry of Organic Natural Products. ProgrèS Dans La Chimie Des Substances Organiques Naturelles. 16: 26-89. PMID 13640068 |
0.65 |
|
| 1958 |
Wiesner K, Valenta Z, Ayer W, Fowler L, Francis J. Annotinine—II Tetrahedron. 4: 87-104. DOI: 10.1016/0040-4020(58)88008-4 |
0.528 |
|
| 1958 |
Wiesner K, Bickelhaupt F, Valenta Z. The structure and substitution of the C-D ring system of delphinine Tetrahedron. 4: 418-423. DOI: 10.1016/0040-4020(58)80062-9 |
0.486 |
|
| 1955 |
Wiesner K, Valenta Z, Manson AJ, Stonner FW. Synthesis of Dimethylapoerysopine and an Approach to the Total Synthesis of the Unrearranged Erythrina Bases Journal of the American Chemical Society. 77: 675-683. DOI: 10.1021/ja01608a040 |
0.339 |
|
| 1952 |
Wiesner K, MacDonald DM, Valenta Z, Armstrong R. PITHECOLOBINE, THE ALKALOID OF PITHECOLOBIUMSAMAN BENTH. I Canadian Journal of Chemistry. 30: 761-772. DOI: 10.1139/v52-091 |
0.636 |
|
| 1952 |
Bartlett MF, Figdor SK, Wiesner K. SYNTHESIS OF PARA-BRIDGED BENZENE COMPOUNDS. III Canadian Journal of Chemistry. 30: 291-294. DOI: 10.1139/v52-040 |
0.304 |
|
| 1949 |
PRELOG V, WIESNER K. [Not Available]. Helvetica Chimica Acta. 32: 453-61. PMID 18116959 DOI: 10.1002/hlca.19490320214 |
0.462 |
|
| 1948 |
PRELOG V, HAFLIGER O, WIESNER K. [Not Available]. Helvetica Chimica Acta. 31: 877-83. PMID 18915727 DOI: 10.1002/Hlca.19480310329 |
0.492 |
|
| 1948 |
PRELOG V, WIESNER K. [Not Available]. Helvetica Chimica Acta. 31: 870-6. PMID 18915726 |
0.462 |
|
| 1948 |
PRELOG V, WIESNER K. [Not Available]. Helvetica Chimica Acta. 31: 1325-41. PMID 18875082 DOI: 10.1002/Hlca.19480310518 |
0.513 |
|
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