Year |
Citation |
Score |
2013 |
Antonio T, Childers SR, Rothman RB, Dersch CM, King C, Kuehne M, Bornmann WG, Eshleman AJ, Janowsky A, Simon ER, Reith ME, Alper K. Effect of Iboga alkaloids on µ-opioid receptor-coupled G protein activation. Plos One. 8: e77262. PMID 24204784 DOI: 10.1371/Journal.Pone.0077262 |
0.493 |
|
2010 |
KUEHNE ME, WANG T, SERAPHIN D. ChemInform Abstract: The Total Synthesis of (.+-.)-Mossambine. Cheminform. 26: no-no. DOI: 10.1002/chin.199540240 |
0.56 |
|
2008 |
Huang N, Jiang T, Wang T, Soukri M, Ganorkar R, Deker B, Léger JM, Madalengoitia J, Kuehne ME. The acyclic dienamine-indoloacrylate addition route to catharanthine Tetrahedron. 64: 9850-9856. DOI: 10.1016/J.Tet.2008.07.044 |
0.587 |
|
2003 |
Kuehne ME, Bornmann WG, Markó I, Qin Y, LeBoulluec KL, Frasier DA, Xu F, Mulamba T, Ensinger CL, Borman LS, Huot AE, Exon C, Bizzarro FT, Cheung JB, Bane SL. Syntheses and biological evaluation of vinblastine congeners Organic and Biomolecular Chemistry. 1: 2120-2136. PMID 12945903 DOI: 10.1039/B209990J |
0.599 |
|
2002 |
Chatterjee SK, Laffray J, Patel P, Ravindra R, Qin Y, Kuehne ME, Bane SL. Interaction of tubulin with a new fluorescent analogue of vinblastine Biochemistry. 41: 14010-14018. PMID 12437358 DOI: 10.1021/Bi026182M |
0.368 |
|
2001 |
Kuehne ME, Qin Y, Huot AE, Bane SL. The syntheses of 16a′-homo-leurosidine and 16a′-homo-vinblastine. Generation of atropisomers Journal of Organic Chemistry. 66: 5317-5328. PMID 11485450 DOI: 10.1021/Jo000250Y |
0.478 |
|
2001 |
Kuehne ME, Cowen SD, Xu F, Borman LS. Syntheses of 5a'-homo-vinblastine and congeners designed to establish structural determinants for isolation of atropisomers. The Journal of Organic Chemistry. 66: 5303-16. PMID 11485449 DOI: 10.1021/Jo000249Z |
0.309 |
|
2001 |
Kuehne ME, Dai W, Li YL. New ferrocenyl chiral auxiliary substituents for amines. Applications to syntheses of mossambine and vinblastine Journal of Organic Chemistry. 66: 1560-1566. PMID 11262098 DOI: 10.1021/Jo001399C |
0.371 |
|
2001 |
Kuehne ME, Wilson TE, Bandarage UK, Dai W, Yu Q. Enantioselective syntheses of coronaridine and 18-methoxycoronaridine Tetrahedron. 57: 2085-2094. DOI: 10.1016/S0040-4020(01)00045-X |
0.339 |
|
2000 |
Kuehne ME, Li YL. A Biomimetic Synthesis of the Pauciflorine A and B Skeleton. Organic Letters. 2: 97. PMID 10814255 DOI: 10.1021/Ol991235M |
0.333 |
|
1999 |
Bandarage UK, Kuehne ME, Glick SD. Total syntheses of racemic albifloranine and its anti-addictive congeners, including 18-methoxycoronaridine Tetrahedron. 55: 9405-9424. DOI: 10.1016/S0040-4020(99)00513-X |
0.381 |
|
1998 |
Kuehne ME, Xu F. Syntheses of strychnan- and aspidospermatan-type alkaloids. 11. Total syntheses of (-)-lochneridine and (-)- and racemic 20-epi-lochneridine Journal of Organic Chemistry. 63: 9434-9439. DOI: 10.1021/Jo981401O |
0.384 |
|
1998 |
Kuehne ME, Xu F. Syntheses of strychnan- and aspidospermatan-type alkaloids. 10. An enantioselective synthesis of (-)-strychnine through the Wieland-Gumlich aldehyde Journal of Organic Chemistry. 63: 9427-9433. DOI: 10.1021/Jo9813989 |
0.35 |
|
1998 |
Kuehne ME, Bandarage UK, Hammach A, Li YL, Wang T. Application of Ferrocenylalkyl Chiral Auxiliaries to Syntheses of Indolenine Alkaloids: Enantioselective Syntheses of Vincadifformine, ψ- And 20-epi-ψ-Vincadifformines, Tabersonine, Ibophyllidine, and Mossambine Journal of Organic Chemistry. 63: 2172-2183. DOI: 10.1021/Jo971838G |
0.569 |
|
1997 |
Kuehne ME, Xu F. Syntheses of Strychnan- and Aspidospermatan-Type Alkaloids. 9.(1) The Enantioselective Generation of Tetracyclic ABCE Intermediates by a Tandem Condensation, [3,3]-Sigmatropic Rearrangement, and Cyclization Sequence. The Journal of Organic Chemistry. 62: 7950-7960. PMID 11671897 DOI: 10.1021/Jo970207J |
0.46 |
|
1996 |
Kuehne ME, Wang T, Seraphin D. Syntheses of Strychnos and Aspidospermatan-Type Alkaloids. 8. Selective Total Syntheses of Mossambine and 14-epi-Mossambine by a Radical Cyclization Reaction(1). The Journal of Organic Chemistry. 61: 7873-7881. PMID 11667746 DOI: 10.1021/Jo961023S |
0.595 |
|
1996 |
Kuehne ME, Wang T, Seraphin D. Syntheses of strychnos and aspidospermatan-type alkaloids. 8. Selective total syntheses of mossambine and 14-epi-mossambine by a radical cyclization reaction Journal of Organic Chemistry. 61: 7873-7881. DOI: 10.1021/jo961023s |
0.562 |
|
1996 |
Kuehne ME, Wang T, Seaton PJ. Total syntheses of vincadifformine, 3-oxovincadifformine, pseudo- and 20-epi-pseudovincadifformine, tabersonine, and Δ18-tabersonine through radical reactions and heck reactions Journal of Organic Chemistry. 61: 6001-6008. DOI: 10.1021/Jo960607R |
0.596 |
|
1996 |
Kuehne ME, Bandarage UK. An alternative enantioselective generation of intermediates in the total synthesis of vinblastine: Enantioselection in secodine-type reactions induced by α-ferrocenylethyl N-substituents Journal of Organic Chemistry. 61: 1175-1179. DOI: 10.1021/Jo951857V |
0.371 |
|
1995 |
Kuehne ME, Wang T, Seraphin D. The Total Synthesis of (±)-Mossambine Synlett. 1995: 557-558. DOI: 10.1055/S-1995-5285 |
0.541 |
|
1995 |
Kuehne ME, Brook CS, Frasier DA, Xu F. Syntheses of Strychnos- and Aspidospermatan-type alkaloids. 7. Total syntheses of lagunamine, isolagunamine, condylocarpine, and isocondylocarpine Journal of Organic Chemistry. 60: 1864-1867. DOI: 10.1021/Jo00111A053 |
0.378 |
|
1994 |
Kuehne ME, Brook CS, Xu F, Parsons R. Total syntheses of strychnos alkaloids Pure and Applied Chemistry. 66: 2095-2098. DOI: 10.1351/pac199466102095 |
0.322 |
|
1994 |
Grazul RM, Kuehne ME. The syntheses of (±)-villagorgin A and villagorgin B Natural Product Letters. 5: 187-195. DOI: 10.1080/10575639408044058 |
0.357 |
|
1994 |
Kuehne ME, Brook CS, Frasier DA. Syntheses of strychnos and aspidospermatan type alkaloids. 4. Formation of the pentacyclic core by an intramolecular Diels Alder reaction Natural Product Letters. 4: 65-72. DOI: 10.1080/10575639408043894 |
0.376 |
|
1994 |
Kuehne ME, Xu F, Brook CS. Syntheses of Strychnos- and Aspidospermatan-Type Alkaloids. 6. Total Syntheses of (.+-.)-Echitamidine, (.+-.)-Alstogustine, (.+-.)-19-epi-Alstogustine, and (.+-.)-Akuammicine The Journal of Organic Chemistry. 59: 7803-7806. DOI: 10.1021/Jo00104A042 |
0.382 |
|
1994 |
Kuehne ME, Brook CS, Frasier DA, Xu F. Syntheses of strychnos- and aspidospermatan-type alkaloids. 5. Total syntheses of (±)-echitamidine and 20-epi- and 19-epi-20-epi-echitamidine Journal of Organic Chemistry. 59: 5977-5982. DOI: 10.1021/Jo00099A029 |
0.327 |
|
1993 |
Borman LS, Bornmann WG, Kuehne ME. Modulation of drug cytotoxicity in wild-type and multidrug-resistant tumor cells by stereoisomeric series of C-20′-vinblastine congeners that lack antimicrotubule activity Cancer Chemotherapy and Pharmacology. 31: 343-349. PMID 8431967 DOI: 10.1007/Bf00686146 |
0.506 |
|
1993 |
Kuehne ME, Xu F. Total synthesis of strychnan and aspidospermatan alkaloids. 3. The total synthesis of (±)-strychnine Journal of Organic Chemistry. 58: 7490-7497. DOI: 10.1021/Jo00078A030 |
0.458 |
|
1993 |
Parsons RL, Berk JD, Kuehne ME. Total syntheses of strychnan- and aspidospermatan-type alkaloids. 2. Generation of 15-(3-furanyl) ABCE tetracyclic intermediates Journal of Organic Chemistry. 58: 7482-7489. DOI: 10.1021/Jo00078A029 |
0.41 |
|
1992 |
Deecher DC, Teitler M, Soderlund DM, Bornmann WG, Kuehne ME, Glick SD. Mechanisms of action of ibogaine and harmaline congeners based on radioligand binding studies Brain Research. 571: 242-247. PMID 1377086 DOI: 10.1016/0006-8993(92)90661-R |
0.481 |
|
1992 |
Bornmann WG, Kuehne ME. A common intermediate providing syntheses of ψ-tabersonine, coronaridine, iboxyphylline, ibophyllidine, vinamidine, and vinblastine Journal of Organic Chemistry. 57: 1752-1760. DOI: 10.1021/Jo00032A029 |
0.6 |
|
1991 |
Kuehne ME, Muth RS. Total syntheses of Yohimbe alkaloids, with stereoselection for the normal, allo, and 3-epiallo series, based on annelations of 4-methoxy-1,2-dihydropyridones Journal of Organic Chemistry. 56: 2701-2712. DOI: 10.1021/Jo00008A025 |
0.395 |
|
1991 |
Kuehne ME, Frasier DA, Spitzer TD. Total syntheses of tubotaiwine and 19,20-dihydro-20-epi-akuammicine Journal of Organic Chemistry. 56: 2696-2700. DOI: 10.1021/Jo00008A024 |
0.401 |
|
1991 |
Kuehne ME, Matson PA, Bornmann WG. Enantioselective syntheses of vinblastine, leurosidine, vincovaline, and 20′-epi-vincovaline Journal of Organic Chemistry. 56: 513-528. DOI: 10.1021/Jo00002A008 |
0.617 |
|
1989 |
Kuehne ME, Pitner JB. Studies in biomimetic alkaloid syntheses. 17. Syntheses of iboxyphylline and related alkaloids Journal of Organic Chemistry. 54: 4553-4569. DOI: 10.1021/Jo00280A021 |
0.42 |
|
1989 |
Kuehne ME, Bornmann WG. Syntheses of 20′-deoxyvinblastine, 20′-deoxyleurosidine, 20′-deoxyvincovaline, 20′-epi-20′-deoxyvincovaline, and 20′-deoxyvincristine and its 20′-epimer through racemic and enantioselectively generated intermediates. New syntheses of D/E-cis- and -trans-ψ-vincadifformines and D/E-cis- and -trans-20-epi-ψ-vincadifformines Journal of Organic Chemistry. 54: 3407-3420. DOI: 10.1021/Jo00275A029 |
0.56 |
|
1989 |
Spitzer T, Kuehne ME, Bornmann W, Anklin C. Heteronuclear correlation via spin-locked zero- and multiple-quantum coherences Journal of Magnetic Resonance (1969). 84: 654-657. DOI: 10.1016/0022-2364(89)90134-0 |
0.451 |
|
1989 |
KUEHNE ME, BORNMANN WG, PARSONS WH, SPITZER TD, BLOUNT JF, ZUBIETA J. ChemInform Abstract: Total Syntheses of (.+-.)-Cephalotaxine (Ia) and (.+-.)-8-Oxocephalotaxine (Ib). Cheminform. 20. DOI: 10.1002/chin.198901265 |
0.547 |
|
1988 |
Kuehne ME, Bornmann WG, Parsons WH, Spitzer TD, Blount JF, Zubieta J. Total syntheses of (.+-.)-cephalotaxine and (.+-.)-8-oxocephalotaxine The Journal of Organic Chemistry. 53: 3439-3450. DOI: 10.1021/Jo00250A008 |
0.578 |
|
1988 |
Kuehne ME, Bornmann WG, Parsons WH, Spitzer TD, Blount JF, Zubieta J. Total syntheses of (±)-cephalotaxine and (±)-8-oxocephalotaxine Journal of Organic Chemistry. 53: 3439-3450. |
0.442 |
|
1987 |
Kuehne ME, Podhorez DE, Mulamba T, Bornmann WG. Biomimetic alkaloid syntheses. 15. Enantioselective syntheses with epichlorohydrin: total syntheses of (+)-, (-)- and (.+-.)-vindoline and a synthesis of (-)-vindorosine Journal of Organic Chemistry. 52: 347-353. DOI: 10.1021/Jo00379A006 |
0.636 |
|
1987 |
Kuehne ME, Zebovitz TC, Bornmann WG, Marko I. Three routes to the critical C16'-C14' parf relative stereochemistry of vinblastine. Syntheses of 20'-desethyl-20'-deoxyvinblastine, and 20'-desethyl-20'-deoxyvincovaline Journal of Organic Chemistry. 52: 4340-4349. DOI: 10.1021/Jo00228A035 |
0.516 |
|
1987 |
Kuehne ME, Zebovitz TC. Studies in biomimetic alkaloid syntheses. 16. Syntheses of D/E trans and cis desethylvincadifformines and of the C16 epimeric carbomethoxydesethyldihydrocleavamines and their isolable piperidine ring conformational isomers Journal of Organic Chemistry. 52: 4331-4339. DOI: 10.1021/Jo00228A034 |
0.337 |
|
1987 |
KUEHNE ME, PODHOREZ DE, MULAMBA T, BORNMANN WG. ChemInform Abstract: Biomimetic Alkaloid Syntheses. Part 15. Enantioselective Syntheses with Epichlorohydrin: Total Syntheses of (+)-, (-)-, and (.+-.)-Vindoline (I) and a Synthesis of (-)-Vindorosine (II). Cheminform. 18. DOI: 10.1002/chin.198735339 |
0.574 |
|
1987 |
Kuehne ME, Podhorez DE, Mulamba T, Bornmann WG. Biomimetic alkaloid syntheses. 15. Enantioselective syntheses with epichlorohydrin: Total syntheses of (+)-, (-)-, and (±)-vindoline and a synthesis of (-)-vindorosine Journal of Organic Chemistry. 52: 347-353. |
0.564 |
|
1987 |
Kuehne ME, Zebovitz TC, Bornmann WG, Marko I. Three routes to the critical C16′-C14′ parf relative stereochemistry of vinblastine. Syntheses of 20′-desethyl-20′-deoxyvinblastine and 20′-desethyl-20′-deoxyvincovaline Journal of Organic Chemistry. 52: 4340-4349. |
0.535 |
|
1986 |
Kuehne ME, Bornmann WG, Earley WG, Marko I. Studies in biomimetic alkaloid syntheses. 14. Controlled, selective syntheses of catharanthine and tabersonine, and related desethyl compounds, through generation of 15-oxosecodine intermediates Journal of Organic Chemistry. 51: 2913-2927. DOI: 10.1021/Jo00365A012 |
0.585 |
|
1986 |
Kuehne ME, Bornmann WG, Earley WG, Marko I. Studies in biomimetic alkaloid syntheses. 14. Controlled, selective syntheses of catharanthine and tabersonine, and related desethyl compounds, through generation of 15-oxosecodine intermediates Journal of Organic Chemistry. 51: 2913-2927. |
0.543 |
|
1985 |
Kuehne ME, Seaton PJ. Studies in biomimetic alkaloid syntheses. 13. Total syntheses of racemic aspidofractine, pleiocarpine, pleiocarpinine, kopsinine, N-methylkopsanone, and kopsanone Journal of Organic Chemistry. 50: 4790-4796. DOI: 10.1021/Jo00224A027 |
0.32 |
|
1985 |
Kuehne ME, Bohnert JC, Bornmann WG, Kirkemo CL, Kuehne SE, Seaton PJ, Zebovitz TC. Biomimetic syntheses of indole alkaloids. 11. Syntheses of .beta.-carboline and indoloazepine intermediates Journal of Organic Chemistry. 50: 919-924. DOI: 10.1021/Jo00207A001 |
0.573 |
|
1985 |
Kuehne ME, Reider PJ. A synthesis of ibogamine Journal of Organic Chemistry. 50: 1464-1467. DOI: 10.1002/Chin.198539346 |
0.379 |
|
1985 |
Kuehne ME, Bohnert JC, Bornmann WG, Kirkemo CL, Kuehne SE, Seaton PJ, Zebovitz TC. BIOMIMETIC SYNTHESES OF INDOLE ALKALOIDS. 11. SYNTHESES OF β-CARBOLINE AND INDOLOAZEPINE INTERMEDIATES Cheminform. 16. DOI: 10.1002/Chin.198535326 |
0.571 |
|
1985 |
Kuehne ME, Podhorez DE. Studies in biomimetic alkaloid syntheses. 12. Enantioselective total syntheses of (-)- and (+)-vincadifformine and of (-)-tabersonine Journal of Organic Chemistry. 50: 924-929. DOI: 10.1002/Chin.198535324 |
0.462 |
|
1985 |
Kuehne ME, Bohnert JC, Bornmann WG, Kirkemo CL, Kuehne SE, Seaton PJ, Zebovitz TC. Biomimetic syntheses of indole alkaloids. 11. Syntheses of β-carboline and indoloazepine intermediates Journal of Organic Chemistry. 50: 919-924. |
0.527 |
|
1983 |
Kuehne ME, Parsons WH. The photochemical or thermal rearrangement of oxaziranes as a method in alkaloid synthesis Tetrahedron. 39: 3763-3765. DOI: 10.1016/S0040-4020(01)88617-8 |
0.35 |
|
1983 |
Kuehne ME, Earley WG. Studies in biomimetic alkaloid syntheses-10. The synthesis of a 19-oxosecodine and its cyclization to minovincine Tetrahedron. 39: 3715-3717. DOI: 10.1016/S0040-4020(01)88610-5 |
0.446 |
|
1983 |
Kuehne ME, Earley WG. Studies in biomimetic alkaloid syntheses-9. Two total syntheses of minovincine Tetrahedron. 39: 3707-3714. DOI: 10.1016/S0040-4020(01)88609-9 |
0.401 |
|
1982 |
Kuehne ME, Okuniewicz FJ, Kirkemo CL, Bohnert JC. Studies in biomimetic alkaloid syntheses. 8. Total syntheses of the C-14 epimeric hydroxyvincadifformines, tabersonine, a (hydroxymethyl)-D-norvincadifformine, and the C-20 epimeric pandolines Journal of Organic Chemistry. 47: 1335-1343. DOI: 10.1021/Jo00346A034 |
0.311 |
|
1981 |
Kuehne ME, Bohnert JC. Studies in biomimetic alkaloid syntheses. 7. Stereospecific total syntheses of ibophyllidine and 20-epiibophyllidine Journal of Organic Chemistry. 46: 3443-3447. DOI: 10.1021/Jo00330A012 |
0.452 |
|
1981 |
Kuehne ME, Matsko TH, Bohnert JC, Motyka L, Oliver-Smith D. Studies in biomimetic alkaloid syntheses. 6. Alternative pathways to secodines and their acyclic enamino acrylate analogues. Total syntheses of desethylibophyllidine, D-norvincadifformine, desethylvincadifformine, 20-methyldesethylvincadifformine, and 3-oxovincadifformine Journal of Organic Chemistry. 46: 2002-2009. DOI: 10.1021/Jo00323A007 |
0.301 |
|
1981 |
KUEHNE ME, MATSKO TH, BOHNERT JC, MOTYKA L, SMITH DO. ChemInform Abstract: STUDIES IN BIOMIMETIC ALKALOID SYNTHESES. 6. ALTERNATIVE PATHWAYS TO SECODINES AND THEIR ACYCLIC ENAMINO ACRYLATE ANALOGS. TOTAL SYNTHESES OF DESETHYLIBOPHYLLIDINE, D-NORVINCADIFFORMINE, DESETHYLVINCADIFFORMINE, 20-METHYLDESETHYLVINCA Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198137341 |
0.371 |
|
1980 |
Kuehne ME, Kirkemo CL, Matsko TH, Bohnert JC. Studies in biomimetic alkaloid syntheses. 5. Studies syntheses of .psi.-vincadifformine, 20-epi-.psi.-vincadifformine, pandoline, 20-epipandoline, and the C-16 epimeric(carbomethoxy)velbanamines The Journal of Organic Chemistry. 45: 3259-3265. DOI: 10.1021/Jo01304A023 |
0.367 |
|
1979 |
Kuehne ME, Matsko TH, Bohnert JC, Kirkemo CL. Studies in biomimetic alkaloid syntheses. 3. Syntheses of ervinceine and vincadifformine analogs from tetrahydro-.gamma.-carbolines through secodine intermediates Journal of Organic Chemistry. 10: 1063-1068. DOI: 10.1021/Jo01321A008 |
0.401 |
|
1979 |
Kuehne ME, Huebner JA, Matsko TH. Studies in biomimetic alkaloid syntheses. 4. An alternative route to secodine intermediates providing syntheses of minovine, vincadifformine, ervinceine, and N(a)-methylervinceine Journal of Organic Chemistry. 44: 2477-2480. DOI: 10.1002/Chin.197946335 |
0.377 |
|
1979 |
Kuehne ME, Matsko TH, Bohnert JC, Kirkemo CL. Studies in biomimetic alkaloid syntheses. 3. Syntheses of ervinceine and vincadifformine analogues from tetrahydro-γ-carbolines through secodine intermediates Journal of Organic Chemistry. 44: 1063-1068. |
0.35 |
|
1978 |
Kuehne ME, Roland DM, Hafter R. Studies in biomimetic alkaloid syntheses. 2. Synthesis of vincadifformine from tetrahydro-.beta.-carboline through a secodine intermediate Journal of Organic Chemistry. 43: 3705-3710. DOI: 10.1021/Jo00413A015 |
0.334 |
|
1978 |
Kuehne ME, Hafter R. Studies in biomimetic alkaloid syntheses. 1. Alkylations of 3-chloroindolenines Journal of Organic Chemistry. 43: 3702-3704. DOI: 10.1021/Jo00413A014 |
0.468 |
|
1978 |
Kuehne ME, Roland DM, Hafter R. Studies in biomimetic alkaloid syntheses. 2. Synthesis of vincadifformine from tetrahydro-β-carboline through a secodine intermediate Journal of Organic Chemistry. 43: 3705-3710. DOI: 10.1002/Chin.197903314 |
0.374 |
|
1974 |
Hollenbeak KH, Kuehne ME. The isolation and structure determination of the fern glycoside osmundalin and the synthesis of its aglycone osmundalactone Tetrahedron. 30: 2307-2316. DOI: 10.1016/S0040-4020(01)97097-8 |
0.333 |
|
1973 |
Kuehne ME, King JC. Cyclopropylamines as intermediates in a new method for alkylation of aldehydes and ketones Journal of Organic Chemistry. 38: 304-311. DOI: 10.1021/Jo00942A022 |
0.324 |
|
1970 |
Kuehne ME, Garbacik T. Relative reactivities of enamines in alkylation reactions Journal of Organic Chemistry. 35: 1555-1558. DOI: 10.1021/Jo00830A063 |
0.308 |
|
1970 |
Kuehne ME, Nelson JA. Stereospecific syntheses of epimeric diterpenoid resin acids through enolate anion reactions Journal of Organic Chemistry. 35: 161-170. DOI: 10.1021/Jo00826A036 |
0.329 |
|
1969 |
Keyton DJ, Griffin GW, Kuehne ME, Bayha CE. The reaction of arynes with enamines: A new ring expansion leading to benzocycloheptenone Tetrahedron Letters. 10: 4163-4168. DOI: 10.1016/S0040-4039(01)88643-3 |
0.317 |
|
1966 |
Kuehne ME, Bayha C. A synthetic route to aspidospermine and quebrachamine Tetrahedron Letters. 7: 1311-1315. DOI: 10.1016/S0040-4039(01)99714-X |
0.307 |
|
1964 |
Kuehne ME, Weaver SJ, Franz P. Enamines as 1,3-dipolarophiles Journal of Organic Chemistry. 29: 1582-1586. DOI: 10.1021/Jo01029A075 |
0.306 |
|
1963 |
Kuehne ME. Reactions of enamines with electrophilic sulfur compounds Journal of Organic Chemistry. 28: 2124-2128. DOI: 10.1021/Jo01043A045 |
0.352 |
|
1959 |
Aldrich PE, Diassi PA, Dickel DF, Dylion CM, Hance PD, Huebner CF, Korzun B, Kuehne ME, Liu LH, MacPhillamy HB, Robb EW, Roychaudhuri DK, Schlittler E, St. André AF, Van Tamelen EE, et al. The stereochemistry of reserpine, deserpidine and related alkaloids Journal of the American Chemical Society. 81: 2481-2494. |
0.47 |
|
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