| Year |
Citation |
Score |
| 2010 |
Vloon WJ, van Den Bos JC, Willard NP, Koomen G, Pandit UK. An alternative synthesis of (+)-sesbanimide A Recueil Des Travaux Chimiques Des Pays-Bas. 110: 414-419. DOI: 10.1002/Recl.19911101005 |
0.399 |
|
| 2010 |
Vega E, de Waard ER, Pandit UK. Reduction of 1-(5-uracilylmethyl)pyridinium salts by thiols to thymine derivatives. A model of the thymidylate synthase reaction Recueil Des Travaux Chimiques Des Pays-Bas. 109: 131-132. DOI: 10.1002/Recl.19901090220 |
0.353 |
|
| 2010 |
Vloon WJ, van den Bos JC, Willard NP, Koomen G, Pandit UK. Synthesis of (+)-sesbanimide a. Structure of the crucial silyl ether AB ring intermediate Recueil Des Travaux Chimiques Des Pays-Bas. 108: 393-394. DOI: 10.1002/Recl.19891081012 |
0.402 |
|
| 2010 |
van Niel JCG, Kort CWF, Pandit UK. NAD(P)H models XXII. Magnesium ion mediated acid catalysis of the reduction of imines by Hantzsch ester Recueil Des Travaux Chimiques Des Pays-Bas. 105: 262-265. DOI: 10.1002/Recl.19861050906 |
0.341 |
|
| 2010 |
Case RA, Pandit UK. NAD(P)H models XV. Reduction of Δ4-3-ketosteroids via their iminium salts, by 1,4-dihydropyridine derivatives Recueil Des Travaux Chimiques Des Pays-Bas. 99: 334-340. DOI: 10.1002/Recl.19800991103 |
0.395 |
|
| 2010 |
Pandit UK, de Nie-Sarink MJ, van der Burg AM, Steevens JB, van Dokkum RFM. α-Amino acid dehydrogenase models. Reduction of an imine and of iminium salts of α-keto esters by 1,4-dihydropyridines (Preliminary communication) Recueil Des Travaux Chimiques Des Pays-Bas. 97: 149-150. DOI: 10.1002/Recl.19780970509 |
0.318 |
|
| 2010 |
Pandit U, Bieräugel H. A facile approach to an optically active tetracyclic intermediate for the synthesis of 6-methyl-19-norsteroids Recueil Des Travaux Chimiques Des Pays-Bas. 95: 223-224. DOI: 10.1002/Recl.19760950910 |
0.325 |
|
| 2010 |
Pandit UK, de Graaf SAG, Braams CT, Raaphorst JST. Functionalized enamines. Part XII: Influence of base-component in the reaction of β-tetralone enamines with carbenes Recueil Des Travaux Chimiques Des Pays-Bas. 91: 799-808. DOI: 10.1002/Recl.19720910706 |
0.349 |
|
| 2010 |
de Koning H, Pandit U. Unconventional nucleotide analogues. V Derivatives of 6-(1-pyrimidinyl)- and 6-(9-purinyl)-2-aminocaproic acid Recueil Des Travaux Chimiques Des Pays-Bas. 90: 874-884. DOI: 10.1002/Recl.19710900807 |
0.341 |
|
| 2010 |
van der Vlugt FA, Verhoeven JW, Pandit UK. Functionalized enamines. Part XI. Steric effects in α-tetralone enamines Recueil Des Travaux Chimiques Des Pays-Bas. 89: 1258-1266. DOI: 10.1002/Recl.19700891205 |
0.376 |
|
| 2010 |
Willems AGM, van Eck RR, Nijhuis H, Pandit UK, Huisman HO. Polynuclear heterocyclic systems: Part VII. Addition of dimethyl azodiformate to 1-arylcycloalkenes Recueil Des Travaux Chimiques Des Pays-Bas. 89: 885-895. DOI: 10.1002/Recl.19700890816 |
0.367 |
|
| 2010 |
de Waard ER, Neeter R, Pandit UK, Huisman HO. Polynuclear heterocyclic systems. Part VI: Synthesis of perhydropyridazo[1,2-a]cinnoline Recueil Des Travaux Chimiques Des Pays-Bas. 87: 572-579. DOI: 10.1002/Recl.19680870510 |
0.41 |
|
| 2010 |
van Hes R, Skolnik S, Pandit UK, Huisman HO. Polynuclear heterocyclic systems. Part V: Heterocycles related to steroids and C-nor-steroids Recueil Des Travaux Chimiques Des Pays-Bas. 87: 151-160. DOI: 10.1002/Recl.19680870206 |
0.325 |
|
| 2010 |
van Hes R, Pandit UK, Huisman HO. Heterocyclic Steroids. Part XI 1-Hydroxy-1-vinylquinolizidine - its synthesis, stereochemistry and attempted conversion to 5-azasteroids Recueil Des Travaux Chimiques Des Pays-Bas. 86: 1255-1262. DOI: 10.1002/Recl.19670861112 |
0.341 |
|
| 2010 |
Pandit UK, Huisman HO. Polynuclear heterocyclic systems. III: Reaction of 2-aminocyclanones with dimethyl acetylenedicarboxylate Recueil Des Travaux Chimiques Des Pays-Bas. 85: 311-322. DOI: 10.1002/Recl.19660850311 |
0.379 |
|
| 2010 |
Willems AGM, Pandit UK, Huisman HO. The dehydrobromination of 1,2-dibromo-1,2,3,4-tetrahydronaphthalene Recueil Des Travaux Chimiques Des Pays-Bas. 84: 389-392. DOI: 10.1002/Recl.19650840315 |
0.369 |
|
| 2010 |
Pandit UK, Huisman HO. A new route to 4,5-dihydro-3H-benz(e)indole systems: Reaction of dimethyl acetylenedicarboxylate with 2-aminotetralone-1 hydrochloride Recueil Des Travaux Chimiques Des Pays-Bas. 83: 50-52. DOI: 10.1002/Recl.19640830106 |
0.309 |
|
| 2010 |
Huisman HO, Speckamp WN, Pandit UK. Total synthesis of aza-steroids I: d,l-N-Tosyl-6-aza-8,14-bisdehydroestrone methyl ether and d,l-N-tosyl-6-aza-8,14-bisdehydro-D-homoestrone methyl ether Recueil Des Travaux Chimiques Des Pays-Bas. 82: 898-900. DOI: 10.1002/Recl.19630820907 |
0.383 |
|
| 2010 |
Speckamp WN, Pandit UK, Huisman HO. Dihydroquinolones I: Reactions of substituted 4-oxo-1,2,3,4-tetrahydroquinoline Recueil Des Travaux Chimiques Des Pays-Bas. 82: 39-48. DOI: 10.1002/Recl.19630820105 |
0.407 |
|
| 1999 |
Madre M, Panchenko N, Golbraikh A, Zhuk R, Pandit UK, Geenevasen J, Koomen GJ. Purine nucleoside analogues. 11. An alternative synthesis of N- and O-alkyl derivatives of 9- and 7-[(2-acetoxyethoxy)methyl]-N2-acetylguanine Collection of Czechoslovak Chemical Communications. 64: 685-695. DOI: 10.1135/Cccc19990685 |
0.622 |
|
| 1999 |
Pandit UK, Overkleeft HS, Borer BC, Bieräugel H. Synthesis mediated by ring-closing metathesis - Applications in the synthesis of azasugars and alkaloids European Journal of Organic Chemistry. 959-968. DOI: 10.1002/(Sici)1099-0690(199905)1999:5<959::Aid-Ejoc959>3.0.Co;2-K |
0.422 |
|
| 1998 |
Overkleeft HS, Renkema GH, Neele J, Vianello P, Hung IO, Strijland A, van der Burg AM, Koomen GJ, Pandit UK, Aerts JM. Generation of specific deoxynojirimycin-type inhibitors of the non-lysosomal glucosylceramidase. The Journal of Biological Chemistry. 273: 26522-7. PMID 9756888 DOI: 10.1074/jbc.273.41.26522 |
0.615 |
|
| 1998 |
Overkleeft HS, Bruggeman P, Pandit UK. Ring-closing metathesis mediated synthesis of pyrrolizidine and quinolizidine azasugars Tetrahedron Letters. 39: 3869-3872. DOI: 10.1016/S0040-4039(98)00635-2 |
0.385 |
|
| 1996 |
Pandit UK, Borer BC, Bieräugel H. Synthetic studies on manzamine A Pure and Applied Chemistry. 68: 659-662. DOI: 10.1351/Pac199668030659 |
0.425 |
|
| 1996 |
Overkleeft HS, Pandit UK. A formal synthesis of castanospermine using an olefin metathesis cyclisation reaction as a key step Tetrahedron Letters. 37: 547-550. DOI: 10.1016/0040-4039(95)02237-6 |
0.455 |
|
| 1995 |
Bieräugel H, Borer BC, Pandit UK. Approaches to the synthesis of manzamine a. synthesis of the β-carboline-bearing abce ring system Heterocyclic Communications. 1: 115-118. DOI: 10.1515/Hc.1995.1.2-3.115 |
0.392 |
|
| 1994 |
Pandit UK, Borer BC, Bieräugel H, Deerenberg S. Studies on the total synthesis of manzamine A Pure and Applied Chemistry. 66: 2131-2134. DOI: 10.1351/Pac199466102131 |
0.414 |
|
| 1994 |
Meissner JWG, van der Laan AC, Pandit UK. Reduction of 5-arylidenebarbiturate derivatives by thiols Tetrahedron Letters. 35: 2757-2760. DOI: 10.1016/S0040-4039(00)77025-0 |
0.373 |
|
| 1994 |
Borer BC, Deerenberg S, Bieräugel H, Pandit UK. The first synthesis of the ABCD ring system of manzamine A. Construction of the macrocyclic ring D Tetrahedron Letters. 35: 3191-3194. DOI: 10.1016/S0040-4039(00)76864-X |
0.393 |
|
| 1994 |
Boogaard AT, Pandit UK, Koome GJ. Ring D modifications of ellipticine. Part 1. New ellipticine derivatives from 1-cyano-6-methylellipticine. Tetrahedron. 50: 2551-2560. DOI: 10.1016/S0040-4020(01)86971-4 |
0.353 |
|
| 1994 |
Overkleeft HS, van Wiltenburg J, Pandit UK. A facile transformation of sugar lactones to azasugars Tetrahedron. 50: 4215-4224. DOI: 10.1016/S0040-4020(01)86715-6 |
0.37 |
|
| 1994 |
Hilhorst E, Iskander AS, Chen TBRA, Pandit UK. Alkyl transfer from quaternary ammonium salts to cobalt (I): Model for the cobalamin-dependent methionine synthase reaction Tetrahedron. 50: 8863-8870. DOI: 10.1016/S0040-4020(01)85359-X |
0.349 |
|
| 1994 |
Hilhorst E, Chen TBRA, Iskander AS, Pandit UK. Dealkylation of quaternary ammonium salts by thiolate anions: A model of the cobalamin-independent methionine synthase reaction. Tetrahedron. 50: 7837-7848. DOI: 10.1016/S0040-4020(01)85267-4 |
0.372 |
|
| 1994 |
Boogaard AT, Pandit UK, Koomen GJ. Ring D modifications of ellipticine. Part 2. Chlorination of ellipticine via its N-oxide and synthesis and selective acetylation of 5,6,11-trimethyl-5H-benzo[b]carbazole. Tetrahedron. 50: 4811-4828. DOI: 10.1016/S0040-4020(01)85018-3 |
0.643 |
|
| 1994 |
Pandit UK. Synthetic strategies directed to the antitumour alkaloids sesbanimide A and manzamine A Journal of Heterocyclic Chemistry. 31: 615-624. DOI: 10.1002/Jhet.5570310303 |
0.405 |
|
| 1993 |
Hilhorst E, Chen TBRA, Pandit UK. A model of the cobalamin-independent methionine synthase reaction Journal of the Chemical Society, Chemical Communications. 881-882. DOI: 10.1039/C39930000881 |
0.31 |
|
| 1993 |
Hilhorst E, Iskander AS, Chen TBRA, Pandit UK. Model studies of the cobalamin-dependent methionine synthase reaction Tetrahedron Letters. 34: 4257-4260. DOI: 10.1016/S0040-4039(00)60542-7 |
0.317 |
|
| 1992 |
Plug JPM, Koomen GJ, Pandit UK. An expedient synthesis of 9-hydroxyellipticine Synthesis. 1221-1222. DOI: 10.1055/S-1992-26342 |
0.621 |
|
| 1992 |
Meissner JWG, Pandit UK. Model studies of the thymidylate synthase reaction. The mechanism of reduction of 5-uracilylmethylenepyridinium salts by benzyl thiol Tetrahedron Letters. 33: 2999-3002. DOI: 10.1016/S0040-4039(00)79582-7 |
0.364 |
|
| 1992 |
van Maarschalkerwaart DAH, Willard NP, Pandit UK. Synthesis of carbohydrate containing crown ethers and their application as catalysts in asymmetric michael additions Tetrahedron. 48: 8825-8840. DOI: 10.1016/S0040-4020(01)89454-0 |
0.362 |
|
| 1992 |
Huizenga RH, Pandit UK. Models of folate cofactors - 24 a route to optically active octahydroindolo[2,3-a]quinolizines Tetrahedron. 48: 6521-6528. DOI: 10.1016/S0040-4020(01)88242-9 |
0.332 |
|
| 1992 |
Vloon WJ, van den Bos JC, Koomen GJ, Pandit UK. Synthesis of ring C modified sesbanimide analogues Tetrahedron. 48: 8317-8328. DOI: 10.1016/S0040-4020(01)80499-3 |
0.635 |
|
| 1992 |
Plug JPM, Koomen GJ, Pandit UK. Sythesis of novel annulated ellipticines via Claisen rearrangement reactions Tetrahedron Letters. 33: 2179-2182. DOI: 10.1016/0040-4039(92)88171-Z |
0.666 |
|
| 1991 |
Brands KMJ, Meekel AAP, Pandit UK. Synthesis of the homochiral "tricyclic heart" of manzamine A Tetrahedron. 47: 2005-2026. DOI: 10.1016/S0040-4020(01)96112-5 |
0.385 |
|
| 1991 |
Vega E, Rood GA, de Waard ER, Pandit UK. Reduction of 5-uracilylmethylenepyridinium salts by thiols. A model of the reduction step of the thymidylate synthase reaction Tetrahedron. 47: 4361-4368. DOI: 10.1016/S0040-4020(01)87105-2 |
0.38 |
|
| 1991 |
Huizenga RH, van Wiltenburg J, Bieräugel H, Pandit UK. Models of folate cofactors - 23. A synthetic strategy to the aspidosperma skeleton. Synthesis of the 21-epimer of 20-deethyl-3,17-dioxo-16-ethoxycarbonyl-1-methylaspidospermidine. Tetrahedron. 47: 4165-4174. DOI: 10.1016/S0040-4020(01)86453-X |
0.424 |
|
| 1991 |
Huizenga RH, Pandit UK. Models of folate cofactors - 22. Lewis acid catalyzed cyclization of carbon-fragment transfer products of folate cofactor models. Synthesis of enantiomerically pure tetracyclic (ABCE) ring system of aspidosperma alkaloids. Tetrahedron. 47: 4155-4164. DOI: 10.1016/S0040-4020(01)86452-8 |
0.424 |
|
| 1991 |
van den Bos JC, Vloon WJ, Koomen GJ, Pandit UK. Synthesis of acyclic analogues of sesbanimides A and B Tetrahedron. 47: 6787-6794. DOI: 10.1016/S0040-4020(01)82330-9 |
0.652 |
|
| 1989 |
Pandit UK. Synthetic studies on sesbanimides Pure and Applied Chemistry. 61: 423-426. DOI: 10.1351/Pac198961030423 |
0.348 |
|
| 1989 |
Huizenga RH, van Wiltenburg J, Pandit UK. A short synthesis of the 21-epimer of the (±)-aspidosperma skeleton Tetrahedron Letters. 30: 7105-7106. DOI: 10.1016/S0040-4039(01)93435-5 |
0.338 |
|
| 1989 |
Brands KMJ, Pandit UK. Synthesis of the "tricyclic heart" of manzamines Tetrahedron Letters. 30: 1423-1426. DOI: 10.1016/S0040-4039(00)99482-6 |
0.389 |
|
| 1989 |
Langendoen A, Plug JPM, Koomen GJ, Pandit UK. Regiospecific C-9 substitution of ellipticine derivatives Tetrahedron. 45: 1759-1762. DOI: 10.1016/S0040-4020(01)80040-5 |
0.622 |
|
| 1989 |
Stoit AR, Pandit UK. Models of folate cofactors 20.2 2 Part 19. P.F.C. van der Meij and U.K. Pandit, Tetrahedron Letters, in press. an approach to deethyleburnamonine Tetrahedron. 45: 849-854. DOI: 10.1016/0040-4020(89)80116-4 |
0.335 |
|
| 1988 |
Bieräugel H, Brands KMJ, Pandit UK. Reactions of 3-acylpyridinium salts with electrophilic olefins. A one-pot ring annelation reaction of pyridines Heterocycles. 27: 1589-1593. DOI: 10.3987/Com-88-4564 |
0.375 |
|
| 1988 |
van der Meij PFC, Pandit UK. Chemical modelling of the thymidylate synthase reaction: evidence for the formation of an exocyclic methylene intermediate from analogues of the covalent ternary complex formed by intramolecular thiol addition to C(6) of 5-aminomethyluracil derivatives. Tetrahedron Letters. 29: 5445-5448. DOI: 10.1016/S0040-4039(00)82891-9 |
0.38 |
|
| 1988 |
Stoit AR, Pandit UK. Models of folate cofactors 18. Application in an approach to the synthesis of indoloquinolizine alkaloids Tetrahedron. 44: 6187-6195. DOI: 10.1016/S0040-4020(01)89808-2 |
0.426 |
|
| 1988 |
Langendoen A, Koomen GJ, Pandit UK. An approach to novel ellipticine glycosides Tetrahedron. 44: 3627-3631. DOI: 10.1016/S0040-4020(01)85992-5 |
0.644 |
|
| 1987 |
Vloon WJ, Kruk C, Pandit UK, Hofs HP, McVie JG. Synthesis and biological properties of side-chain-modified bleomycins. Journal of Medicinal Chemistry. 30: 20-4. PMID 2433447 DOI: 10.1021/Jm00384A003 |
0.331 |
|
| 1987 |
Langendoen A, Koomen GJ, Pandit UK. A new approach to C-9 hydroxylation of N(6)-substituted ellipticine Heterocycles. 26: 91-94. DOI: 10.3987/R-1987-01-0091 |
0.604 |
|
| 1987 |
Langendoen A, Koomen GJ, Pandit UK. Side-chain substitution of 6-methylellipticine approach to a new class of ellipticine derivatives Heterocycles. 26: 69-73. DOI: 10.3987/R-1987-01-0069 |
0.587 |
|
| 1987 |
Van Der Meij PFC, Chen TBRA, Hilhorst E, De Waard ER, Pandit UK. The first example of a mimic of the overall thymidylate synthase reaction Journal of the Chemical Society, Chemical Communications. 720-721. DOI: 10.1039/C39870000720 |
0.343 |
|
| 1987 |
Van Der Meij PFC, Chen TBRA, Hilhorst E, De Waard ER, Pandit UK. Models of folate cofactors 171 1 Part 16. P.F.C. van der MeiJ, R.D. Lohmann, E.R. de Waard, T.B.R.A. Chen and U.K. Pandit, Tetrahedron 42, 3921 (1986). Methylation of 1,3-dimethyl-6-methylamino-uracil by a 5,10-CH2 -H4folate model. the first mimic of the overall dTMP synthase reaction Tetrahedron. 43: 4015-4021. DOI: 10.1016/S0040-4020(01)81684-7 |
0.369 |
|
| 1987 |
Wanner MJ, Willard NP, Koomen GJ, Pandit UK. Stereospecific synthesis of (+)- and (-)-sesbanimide A Tetrahedron. 43: 2549-2556. DOI: 10.1016/S0040-4020(01)81662-8 |
0.633 |
|
| 1986 |
Van Der Meij PFC, Lohmann RD, De Waard ER, Chen TBRA, Pandit UK. Models of folate coenzymes 161 1 Part 15. A.R. Stoit and U.K. Pandit, Heterocycles, 1986, in press. Chemical modelling of the thymidylate synthase reaction. Evidence for an "exocyclic methylene intermediate" analogue, which is reducible to a thymine derivative, in the reaction of 6-aminouracils with a 5,10-methylenetetrahydrofolate model Tetrahedron. 42: 3921-3930. DOI: 10.1016/S0040-4020(01)87547-5 |
0.392 |
|
| 1986 |
Wijsmuller WFA, Wanner MJ, Koomen GJ, Pandit UK. Pyridocarbazole alkaloids. Synthesis of olivacine and ellipticine analogues Heterocycles. 24: 1795-1797. DOI: 10.1002/Chin.198647359 |
0.662 |
|
| 1986 |
Koomen GJ, Wolschrijn H, van Rhijn JBM, Wanner MJ, Pandit UK. Synthesis of 5-fluoro-3-(2-tetrahydrofuryl)-6-vinyluracil. Design of a 5-fu-derivative with extended conjugation Heterocycles. 24: 939-941. DOI: 10.1002/Chin.198642214 |
0.622 |
|
| 1986 |
Wanner MJ, Willard NP, Koomen GJ, Pandit UK. Synthesis of (7R,8S,9R,10S,11S)-sesbanimide A Journal of the Chemical Society - Series Chemical Communications. 396-397. DOI: 10.1002/Chin.198634331 |
0.553 |
|
| 1985 |
Koomen GJ, van Rhijn JBMv, Pandit UK. Non-glycosidic derivatives of 5-fluorouracil Nucleosides and Nucleotides. 4: 215-216. DOI: 10.1080/07328318508077858 |
0.542 |
|
| 1985 |
Stoit AR, Pandit UK. Models of folate coenzymes 141 1 Part 13. A.R. Stoit and U.K. Pandit, Tetrahedron, preceding paper. An alternate approach to the yohimbane skeleton Tetrahedron. 41: 3355-3361. DOI: 10.1016/S0040-4020(01)96687-6 |
0.35 |
|
| 1985 |
Stott AR, Pandit UK. Models of folate coenzymes 13. Syntheses of benzo[a]quinolizine and indolo[2,3-a]quinolizine derivatives via carbon fragment transfer from folate coenzyme models Tetrahedron. 41: 3345-3354. DOI: 10.1016/S0040-4020(01)96686-4 |
0.3 |
|
| 1985 |
Meijer LHP, Pandit UK. NAD(P)H Models 201 1 NAD(P)H MODELS 19. See L.H.P. Meijer J.C.G. van Niel U.K. Pandit Tetrahedron 40 (1984). Chemoselective metal ion catalyzed reduction of α-keto-β,γ-unsaturated esters by 1,4-dihydropyridine derivatives Tetrahedron. 41: 467-472. DOI: 10.1016/S0040-4020(01)96440-3 |
0.346 |
|
| 1985 |
Van Niel JCG, Pandit UK. Nadh models. XXI.1 1 Part XX. L.H.P. Meijer and U.K. Pandit, Tetrahedron 41, 467 (1985). Stereoselective reduction of chiral imines with hantzsch ester Tetrahedron. 41: 6005-6011. DOI: 10.1016/S0040-4020(01)91441-3 |
0.335 |
|
| 1985 |
Van Der Meij PFC, Lohmann RD, De Waard ER, Chen TBRA, Pandit UK. A chemical model of thymidylate synthetase. Formation of a thymine derivative via an exocylic methylene intermediate Journal of the Chemical Society, Chemical Communications. 1229-1230. DOI: 10.1002/Chin.198601219 |
0.321 |
|
| 1984 |
Pandit UK, Bieräugel H, Stoit AR. An approach to vindoline skeleton utilizing substituted methylenetetrahydrofolate (5,10-CHR-THF) models Tetrahedron Letters. 25: 1513-1516. DOI: 10.1016/S0040-4039(01)80200-8 |
0.416 |
|
| 1984 |
H.P. Meuer L, Johannes C, Niel V, K.Pandit U. Nadh models-19 Tetrahedron. 40: 5185-5195. DOI: 10.1016/S0040-4020(01)91269-4 |
0.398 |
|
| 1984 |
Eling B, Challa G, Pandit UK. A regenerable immobilized NADH model. II. Reduction of α,α,α-trifluoroacetophenone by immobilized 1,4-dihydronicotinamide in aprotic solvent Journal of Polymer Science: Polymer Chemistry Edition. 22: 1945-1962. DOI: 10.1002/Pol.1984.170220901 |
0.312 |
|
| 1984 |
WANNER MJ, KOOMEN G, PANDIT UK. ChemInform Abstract: STUDIES IN THE STEREOSPECIFIC SYNTHESIS OF SESBANIMIDE. SYNTHESIS OF 4-SACCHARIDALGLUTARIMIDES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198448332 |
0.662 |
|
| 1984 |
Vloon WJ, Kruk C, Pandit UK, Hofs HP, Mcvie JG. Modified Bleomycins. Synthesis Of New Bleomycins Via Reaction Of Demethyl-Blm A2 With Bromoacetyl Derivatives Heterocycles. 22: 779-783. DOI: 10.1002/Chin.198440340 |
0.352 |
|
| 1983 |
Van Niel JCG, Pandit UK. Mechanism of hydrogen transfer in the reduction of the imine bond by an NADH model. Use of cyclopropane ring as a chemical probe Journal of the Chemical Society, Chemical Communications. 149-150. DOI: 10.1039/C39830000149 |
0.334 |
|
| 1983 |
Steevens JB, Pandit UK. Nad(p)h models-xvii1 1 For Part XVI, Heterocycles 16, 1687 (1981). Metal ion catalyzed reduction of imines by 3,5-diethoxycarbonyl 2,6-dimethyl-1,4-dihydropyridine (hantzsch ester) Tetrahedron. 39: 1395-1400. DOI: 10.1016/S0040-4020(01)91910-6 |
0.319 |
|
| 1983 |
Bieräugel H, Plemp R, Pandit UK. Models of folate coenzymes-IX. Synthesis of d,l-pyridindolol Tetrahedron. 39: 3987-3989. DOI: 10.1016/S0040-4020(01)90905-6 |
0.338 |
|
| 1983 |
Hiemstra HC, Bieräugel H, Wijnberg M, Pandit UK. Models of folate coenzymes-VIII. An approach to yohimbane alkaloids via carbon-fragment transfer from N5, N10-methylenetetrahydrofolate models Tetrahedron. 39: 3981-3986. DOI: 10.1016/S0040-4020(01)90904-4 |
0.42 |
|
| 1983 |
Bieräugel H, Plemp R, Hiemstra HC, Pandit UK. Models of folate coenzymes-VII. Synthesis and carbon transfer reactions of N5,N10-methenyl and N5,N10-methylenetetrahydrofolate models Tetrahedron. 39: 3971-3979. DOI: 10.1016/S0040-4020(01)90903-2 |
0.394 |
|
| 1983 |
Wanner MJ, Koomen GJ, Pandit UK. Inter- and intramolecular addition of ester anions to nicotinium salts. A facile approach to nauclefine and ellipticine derivatives Tetrahedron. 39: 3673-3681. DOI: 10.1016/S0040-4020(01)88606-3 |
0.674 |
|
| 1983 |
WANNER MJ, KOOMEN G, PANDIT UK. ChemInform Abstract: A CONVENIENT SYNTHESIS OF 6-METHYLELLIPTICINE AND 6-METHYLOLIVACINE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198322343 |
0.666 |
|
| 1982 |
Hiemstra HC, Bieräugel H, Pandit UK. Transfer of functionalized carbon fragments via substituted 5, 10-methylentetetrahydrofolate models. Approach to dihydroindole and indole alkaloids. Tetrahedron Letters. 23: 3301-3304. DOI: 10.1016/S0040-4039(00)87598-X |
0.386 |
|
| 1982 |
Kanner CB, Pandit UK. Functionalized enamines-XXXII. Reaction of β-amino-α, β-unsaturated esters and amides with benzyl and cinnamyl bromides Tetrahedron. 38: 3597-3604. DOI: 10.1016/0040-4020(82)80066-5 |
0.408 |
|
| 1982 |
Wanner MJ, Koomen GJ, Pandit UK. Synthesis of polynuclear heterocycles via the reaction of α-ester carbanions with quaternized nicotinamide salts. A facile stereoselective synthesis of sesbanine Tetrahedron. 38: 2741-2748. DOI: 10.1016/0040-4020(82)80032-X |
0.681 |
|
| 1982 |
WANNER MJ, KOOMEN G, PANDIT UK. ChemInform Abstract: A New Approach to Ellipticine Analogues; Synthesis of 11-Hydroxy-5,6-dimethyl-pyrido[4,3-b]carbazole. Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198233202 |
0.641 |
|
| 1982 |
KEIJZER PC, OUDEMAN A, VAN DER BURG AM, PANDIT UK. ChemInform Abstract: NOVEL NADH MODELS. PART XVI. STEROIDS BEARING PENDENT 1,4-DIHYDRONICOTINAMIDES Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198212345 |
0.308 |
|
| 1982 |
Kanner CB, Pandit UK. FUNCTIONALIZED ENAMINES. PART XXX. REACTION OF β-AMINO-α,β-UNSATURATED ESTERS AND AMIDES WITH ARYL DIAZONIUM SALTS. SYNTHESIS OF CINNOLINE DERIVATIVES Cheminform. 13. DOI: 10.1002/Chin.198204129 |
0.358 |
|
| 1982 |
Kanner CB, Pandit UK. Functionalized Enamines. Part Xxxi. Base-Catalyzed Transformations Of Iminium M Phenylhydrazones. A New Convenient Synthesis Of Imidazo(1,2A)Azacycloalkanes Cheminform. 13. DOI: 10.1002/Chin.198204091 |
0.338 |
|
| 1981 |
Kanner CB, Pandit UK. Base-catalyzed transformations of iminium phenylhydrazones. A new convenient synthesis of imidazo[1,2a]azacycloalkanes1 1 Functionalized Enamines-XXXI. For Part XXX see adjoining paper. Preliminary communication, C.B. Kanner and U.K. Pandit, Heterocycles 9, 757 (1978). Tetrahedron. 37: 3519-3523. DOI: 10.1016/S0040-4020(01)98869-6 |
0.451 |
|
| 1981 |
Kanner CB, Pandit UK. Reaction of β-amino-α,β-unsaturated esters and amides with aryl diazonium salts. Synthesis of cinnoline derivatives Tetrahedron. 37: 3513-3518. DOI: 10.1016/S0040-4020(01)98868-4 |
0.434 |
|
| 1980 |
Wanner MJ, Hageman JJ, Koomen GJ, Pandit UK. Potential carcinostatics. 4. Synthesis and biological properties of erythro- and threo-beta-fluoroaspartic acid and erythro-beta-fluoroasparagine. Journal of Medicinal Chemistry. 23: 85-7. PMID 7359517 DOI: 10.1021/Jm00175A017 |
0.605 |
|
| 1980 |
Rob F, van Ramesdonk HJ, Verhoeven JW, Pandit UK, de Boer TJ. Pyridine-dinucleotide models IV; stereoselective hydride transfer at a bridged pyridinium-ion Tetrahedron Letters. 21: 1549-1552. DOI: 10.1016/S0040-4039(00)92771-0 |
0.328 |
|
| 1980 |
Walraven HGM, Pandit UK. A facile two synthon approach to the camptothecin skeleton Tetrahedron. 36: 321-327. DOI: 10.1016/0040-4020(80)80022-6 |
0.424 |
|
| 1980 |
Soetens HP, Pandit UK. Functionalized enamines XXIX. Solvolytic transformations of 2-methylisoquinolin-1-one dichlorocarbene adduct. Synthesis of benzazepinones Recueil Des Travaux Chimiques Des Pays-Bas. 99: 271-274. DOI: 10.1002/Recl.19800990905 |
0.36 |
|
| 1980 |
Wanner MJ, Van Wijk EM, Koomen GJ, Pandit UK. Potential carcinostatics. V. Synthesis and properties of potential inhibitors of the adenylosuccinate synthetase and adenylosuccinate lyase system Recueil Des Travaux Chimiques Des Pays Bas. 99: 20-23. DOI: 10.1002/Recl.19780970711 |
0.654 |
|
| 1980 |
Bieraeugel H, Plemp R, Pandit UK. Transfer Of A Functionalized Carbon-Fragment Via A Substituted N5,N10-Methylenetetrahydrofolic Acid Model. An Approach To D,L-Pyridindolol Cheminform. 11: 947. DOI: 10.1002/Chin.198052343 |
0.301 |
|
| 1980 |
Soetens HP, Pandit UK. Functionalized Enamines. Xxix. Solvolytic Transformations Of 2‐Methylisoquinolin‐1‐One Dichlorocarbene Adduct. Synthesis Of Benzazepinones Cheminform. 11. DOI: 10.1002/Chin.198051230 |
0.312 |
|
| 1980 |
Wanner MJ, Hageman JJM, Koomen GJ, Pandit UK. POTENTIAL CARCINOSTATICS. 4. SYNTHESIS AND BIOLOGICAL PROPERTIES OF ERYTHRO- AND THREO-β-FLUOROASPARTIC ACID AND ERYTHRO-β-FLUOROASPARAGINE Cheminform. 11. DOI: 10.1002/Chin.198024111 |
0.577 |
|
| 1979 |
de Nie-Sarink MJ, Pandit UK. Chemioselectivity of the reduction of phenyl-substituted α,β-unsaturated iminium salts by an nadh model Tetrahedron Letters. 20: 2449-2452. DOI: 10.1016/S0040-4039(01)86317-6 |
0.316 |
|
| 1979 |
Bieraugel H, Pandit UK. Functionalized enamines XXVIII. A facile synthesis of 6-methyl-19-norsteroids Recueil Des Travaux Chimiques Des Pays Bas. 98: 496-498. DOI: 10.1002/Recl.19790980906 |
0.37 |
|
| 1979 |
de Nie-Sarink M, Pandit U. The reductive animation of 4-tert
-butylcyclohexanone with an NADH model Recueil Des Travaux Chimiques Des Pays-Bas. 98: 162-164. DOI: 10.1002/Recl.19790980404 |
0.397 |
|
| 1979 |
ODIJK WM, WANNER MJ, KOOMEN GJ, PANDIT UK. ChemInform Abstract: POTENTIAL CARCINOSTATIC AGENTS. PART III. PSEUDO-GLYCOSIDIC DERIVATIVES OF 5-FLUOROURACIL Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197909223 |
0.587 |
|
| 1979 |
Kanner CB, Pandit UK. Functionalized Enamines, Xxvi. Reaction Of Conjugated Enamines With Diazonium Salts. A Convenient Synthesis Of Cinnoline Derivatives Cheminform. 10. DOI: 10.1002/Chin.197909221 |
0.416 |
|
| 1978 |
Kanner CB, Pandit UK. Functionalized Enamines. Xxv. Reaction Of Enamine Esters With Diazonium Salts. A Facile One-Pot Synthesis Of Imidazo(1,2A)Azacycloalkanes Cheminform. 9. DOI: 10.1002/Chin.197847184 |
0.401 |
|
| 1978 |
Wanner MJ, Hageman JJM, Koomen GJ, Pandit UK. Potential Carcinostatics. Part Ii. Synthesis And Properties Of Potential Inhibitors Of The Adenylosuccinate Synthetase And Adenylosuccinate Lyase Systems Cheminform. 11. DOI: 10.1002/Chin.197843246 |
0.587 |
|
| 1978 |
van Ramesdonk HJ, Verhoeven JW, Pandit UK, de Boer TJ. Asymmetric reductions by a chiral pyridine-dinucleotide model Recueil Des Travaux Chimiques Des Pays-Bas. 97: 195-196. DOI: 10.1002/Chin.197843074 |
0.303 |
|
| 1978 |
SOETENS H, PANDIT UK. ChemInform Abstract: PHOTOCYCLIZATION OF 4-SUBSTITUTED ISOQUINOLINONE. AN APPROACH TO THE SYNTHESIS OF PHENANTHRIDINE ALKALOIDS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197819187 |
0.314 |
|
| 1978 |
HAGEMAN JJM, WANNER MJ, KOOMEN GJ, PANDIT UK. ChemInform Abstract: POTENTIAL CARCINOSTATICS. SYNTHESIS AND BIOLOGICAL PROPERTIES OF D- AND L-β,β-DIFLUOROASPARTIC ACID AND β,β-DIFLUOROASPARAGINE Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197816128 |
0.567 |
|
| 1978 |
Wanner MJ, Hageman JJM, Koomen GJ, Pandit UK. Potential carcinostatics. Synthesis and properties of potential inhibitors of the adenylosuccinate synthetase and adenylosuccinate lyase systems Recueil Des Travaux Chimiques Des Pays Bas. 97: 211-214. |
0.544 |
|
| 1977 |
Hageman JJ, Wanner MJ, Koomen GJ, Pandit UK. Potential carcinostatics. Synthesis and biological properties of d- and 1-beta,beta-difluoroaspartic acid and beta,beta-difluoroasparagine. Journal of Medicinal Chemistry. 20: 1677-9. PMID 592334 DOI: 10.1021/Jm00222A029 |
0.543 |
|
| 1977 |
Armande JCL, Pandit UK. Alkylation of 3-pyrrolines. A Facile entry into the 12-Aza-Prostanoid Skeleton Tetrahedron Letters. 18: 897-898. DOI: 10.1016/S0040-4039(01)92785-6 |
0.394 |
|
| 1977 |
Thiellier HPM, Koomen GJ, Pandit UK. Unconventional nucleotide analogues1 1 Part XV. H.P.M Thiellier, G.J. Koomen and U.K. Pandit, Heterocycles 5, 19 (1976). Reaction of carbenes with uracil and uridine derivatives Tetrahedron. 33: 1493-1500. DOI: 10.1016/0040-4020(77)88011-3 |
0.633 |
|
| 1977 |
Thiellier HPM, Koomen GJ, Pandit UK. Unconventional nucleotide analogues-XVIII1 1 Part XVII. H.P.M. Thiellier, G.J. Koomen and U.K. Pandit, Tetrahedron 33, 2603 (1977). Ring expansion of uridine halocarbene adducts. Synthesis of diazepine nucleosides Tetrahedron. 33: 2609-2612. DOI: 10.1016/0040-4020(77)80087-2 |
0.648 |
|
| 1977 |
Thiellier HPM, Koomen GJ, Pandit UK. Unconventional nucleotide analogues-XVII1 1 Part XVI. H.P.M. Thiellier, G.J. Koomen and U.K. Pandit, Tetrahedron 33, 1493 (1977). Ring-transformations of uracil dihalocarbene adducts Tetrahedron. 33: 2603-2607. DOI: 10.1016/0040-4020(77)80086-0 |
0.633 |
|
| 1977 |
Bieraeugel H, Soetens HP, Pandit UK. A Facile Synthesis Of 3-Benzazepine And Dibenzazonine Derivatives Cheminform. 7: 37. DOI: 10.1002/Chin.197813231 |
0.424 |
|
| 1977 |
THIELLIER HPM, KOOMEN GJ, PANDIT UK. ChemInform Abstract: UNCONVENTIONAL NUCLEOTIDE ANALOGS. XV. NOVEL BASE-MODIFIED NUCLEOSIDES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197717341 |
0.594 |
|
| 1976 |
Pandit UK, Keijzer PC, Gase RA. Reduction of a thiol ester by dihydropyridine derivatives. A model reaction of glyceraldehyde-3-phosphate dehydrogenase Journal of the Chemical Society, Chemical Communications. 493-494. DOI: 10.1039/C39760000493 |
0.302 |
|
| 1976 |
THIELLIER HPM, KOOMEN GJ, PANDIT UK. ChemInform Abstract: TRANSFORMATIONS OF 1,3-DISUBSTITUTED URACIL-CARBENE ADDUCTS. RING EXPANSION TO 1,3-DIAZEPINE DERIVATIVES Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197603227 |
0.618 |
|
| 1975 |
Pandit UK, Gase RA, Cabré FRM, De Nie-Sarink MJ. Reduction of the ≻C=N≺ bond by an NADH model Journal of the Chemical Society, Chemical Communications. 211-212. DOI: 10.1039/C39750000211 |
0.336 |
|
| 1975 |
Manhas MS, Brown JW, Pandit UK, Houdewind P. Functionalized enamines-XXII. Annelation of enamines of polycyclic α,β-unsaturated ketones; a facile partial synthesis of furano- indolo- and benzsteroids. Total synthesis of 3-oxa-A-norsteroid Tetrahedron. 31: 1325-1330. DOI: 10.1016/0040-4020(75)80178-5 |
0.417 |
|
| 1974 |
Pandit UK, Cabré FRM, Gase RA, De Nie-Sarink MJ. Biomimetic stereospecific reduction of αβ-unsaturated iminium salts Journal of the Chemical Society, Chemical Communications. 627b-628. DOI: 10.1039/C3974000627B |
0.391 |
|
| 1974 |
Houdewind P, Pandit UK. Reaction of dienamines with allylic halides. A case of facile multiple aza-cope rearrangement Tetrahedron Letters. 15: 2359-2362. DOI: 10.1016/S0040-4039(01)92254-3 |
0.319 |
|
| 1974 |
Houdewind P, Armande JCL, Pandit UK. A simple ring annelation of BI- and polycyclic α,β-unsaturated ketones. A facile route to benz[4,5,6]steroids Tetrahedron Letters. 15: 591-594. DOI: 10.1016/S0040-4039(01)82279-6 |
0.337 |
|
| 1974 |
De Graaf SAG, Pandit UK. Functionalized enamines-XVII. Ring expansion of α,β-unsaturated cyclic ketones by reaction of pyrrolidine dienamines with dihalocarbenes; Synthesis of A-homo-steroids Tetrahedron. 30: 1115-1119. DOI: 10.1016/S0040-4020(01)97277-1 |
0.421 |
|
| 1974 |
THIELLIER HPM, BURG AMVD, KOOMEN GJ, PANDIT UK. ChemInform Abstract: REACTION OF CARBENES WITH 1,3-DISUBSTITUTED URACIL DERIVATIVES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197451349 |
0.634 |
|
| 1974 |
HOUDEWIND P, PANDIT UK. ChemInform Abstract: REACTION OF DIENAMINES WITH ALLYLIC HALIDES, FUNCTIONALIZED ENAMINES PART 14, A CASE OF FACILE MULTIPLE AZA-COPE REARRANGEMENT Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197440234 |
0.342 |
|
| 1974 |
Kaspersen FM, Bieraeugel H, Pandit UK. Synthesis Of A Non-Saccharidal Analog Of Puromycin Cheminform. 2: 15. DOI: 10.1002/Chin.197437425 |
0.39 |
|
| 1973 |
Koomen GJ, Pandit UK. Unconventional nucleotide analogues. IX. N-substituted 3-(pyrimidin-1-yl) pyrrolidin-2-ones. Journal of the Chemical Society. Perkin Transactions 1. 17: 1929-33. PMID 4799178 DOI: 10.1039/P19730001929 |
0.621 |
|
| 1973 |
Koomen GJ, Kroon AP, Mas Cabré FR, Goores AP, Peereboom R, Pandit UK. Unconventional nucleotide analogues. Part X. Synthesis of N-substituted 3-(Adenin-9-yl)pyrrolidin-2-ones Journal of the Chemical Society, Perkin Transactions 1. 1934-1940. PMID 4363162 DOI: 10.1039/P19730001934 |
0.649 |
|
| 1973 |
Pandit UK, Steevens JB, Cabré FRM. NADH models. II. Mechanism of reduction of electrophilic olefins with 3,5-diethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine (1) Bioorganic Chemistry. 2: 293-300. DOI: 10.1016/0045-2068(73)90030-8 |
0.336 |
|
| 1973 |
de Graaf SAG, Pandit UK. Functionalized enamines-XV. Reactivity patterns of carbene addition to morpholine enamine of 1-β-acetoxy-6-oxo-8a-methyl-Δ4a(5)-octalin Tetrahedron. 29: 4263-4270. DOI: 10.1016/0040-4020(73)80268-6 |
0.4 |
|
| 1973 |
de Graaf SAG, Pandit UK. Functionalized enamines-XIV. Reaction of α-tetralone enamines with carbenes influence of the nature of carbene and the base-component of the enamine on the reaction pattern Tetrahedron. 29: 2141-2146. DOI: 10.1016/0040-4020(73)80155-3 |
0.377 |
|
| 1973 |
KOOMEN GJ, PANDIT UK. ChemInform Abstract: UNCONVENTIONAL NUCLEOTIDE ANALOGUES PART 9, N-SUBSTITUTED 3-(PYRIMIDIN-1-YL)-PYRROLIDIN-2-ONES Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/chin.197349468 |
0.605 |
|
| 1972 |
PANDIT UK, DE GRAAF SAG. ChemInform Abstract: DIE FRAGE DER QUASI-ENAMIN-REAKTIVITAET VON AMINO-CYCLOPROPANEN, UMLAGERUNG ISOMERER 1-MORPHOLINO-7-CHLOR-7-PHENYL-BICYCLO(4,1,0)HEPTANE Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197251361 |
0.351 |
|
| 1971 |
Koomen GJ, Kroon AP, Goores AP, Pandit UK. Non-Sacccfaridal Nucleoside and Hucleotide Analocuses Synthetic Communications. 1: 41-45. DOI: 10.1080/00397917108081615 |
0.499 |
|
| 1971 |
de Koning H, Pandit U. Unconventional nucleotide analogues. VI. Synthesis of Purinyl- and Pyrimidinyl-Peptides Recueil Des Travaux Chimiques Des Pays-Bas. 90: 1069-1080. DOI: 10.1002/Recl.19710901003 |
0.329 |
|
| 1971 |
EVERS H, PANDIT UK, HUISMAN HO. ChemInform Abstract: EIN EINFACHER SYNTH.-WEG ZU 5,10-DIAZASTEROIDEN 26. MITT. UEBER HETEROCYCLISCHE STEROIDE Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/CHIN.197152386 |
0.569 |
|
| 1971 |
DE KONING H, PANDIT UK. ChemInform Abstract: UNKONVENTIONELLE NUCLEOTID-ANALOGE 6. MITT. SYNTH. VON PURINYL- UND PYRIMIDINYL-PEPTIDEN Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197148386 |
0.307 |
|
| 1971 |
DE KONING H, PANDIT UK. ChemInform Abstract: UNKONVENTIONELLE NUCLEOTID-ANALOGA 5. MITT. DERIVATE VON 6-(PYRIMIDINYL-(1))- UND 6-(PURINYL-(9))-2-AMINO-CAPRONSAEURE Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197145361 |
0.326 |
|
| 1971 |
KOOMEN GJ, KROON AP, GOORES AP, PANDIT UK. ChemInform Abstract: ZUCKERFREIE NUCLEOSID- UND NUCLEOTID-ANALOGA Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197139334 |
0.587 |
|
| 1971 |
WILLE HJ, PANDIT UK, HUISMAN HO. ChemInform Abstract: HETEROCYCLISCHE STEROIDE 20. MITT. EIN LEICHTER ZUGANG ZU 10-AZASTEROIDEN Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197105384 |
0.608 |
|
| 1970 |
Pandit UK, De Graaf SAG. Ring-expansion of cyclic ketones via reaction of enamines with carbenes. Synthesis of A-homo-steroids Journal of the Chemical Society D: Chemical Communications. 381a. DOI: 10.1039/C2970000381A |
0.412 |
|
| 1970 |
Wille HJ, Pandit UK, Huisman HO. Heterocyclic steroids - XX a facile approach to 10-aza-steroids Tetrahedron Letters. 11: 4429-4432. DOI: 10.1016/S0040-4039(00)89450-2 |
0.598 |
|
| 1970 |
Pandit UK, Reus HR, de Jonge K. Functionalized enamines. Part IX: Synthesis of fused furan systems via
reaction of conjugated enamines with α-halogenoketones Recueil Des Travaux Chimiques Des Pays-Bas. 89: 956-960. DOI: 10.1002/Recl.19700890909 |
0.402 |
|
| 1970 |
Pollmann MJM, Pandit UK, Huisman HO. Functionalized enamines. Part VIII: Application of dienamines in the synthesis of 6,7-diazasteroids and polynuclear heterocycles Recueil Des Travaux Chimiques Des Pays-Bas. 89: 941-955. DOI: 10.1002/Recl.19700890908 |
0.348 |
|
| 1970 |
Pollmann MJM, Reus HR, Pandit UK, Huisman HO. Functionalized enamines. Part VII: Reaction of dienamines with arenediazonium salts; Synthesis of 6,7-diaza-D-homoequilenin methyl e her Recueil Des Travaux Chimiques Des Pays-Bas. 89: 929-940. DOI: 10.1002/Recl.19700890907 |
0.404 |
|
| 1970 |
POLLMANN MJM, PANDIT UK, HUISMAN HO. ChemInform Abstract: FUNKTIONATISIERTE ENAMINE 8. MITT. VERWENDUNG VON DIENAMINEN BEI DER SYNTH. VON 6,7-DIAZASTEROIDEN UND MEHRKERNIGEN HETEROCYCLEN Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197050419 |
0.59 |
|
| 1970 |
POLLMANN MJM, REUS HR, PANDIT UK, HUISMAN HO. ChemInform Abstract: FUNKTIONATISIERTE ENAMINE 7. MITT. RK. VON DIENAMINEN MIT ARENDIAZONIUMSALZEN, SYNTH. VON 6,7-DIAZA-D-HOMOEQUILENINMETHYLAETHER Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197050418 |
0.569 |
|
| 1970 |
WILLEMS AGM, VAN ECK RR, NIJHUIS H, PANDIT UK, HUISMAN HO. ChemInform Abstract: VIELKERNIGE HETEROCYCLISCHE SYST. 7. MITT. ADDITION VON DIMETHYLAZODIFORMIAT AN 1-ARYL-CYCLOALKENE Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197050257 |
0.65 |
|
| 1969 |
Nollet AJ, Pandit UK. Unconventional nucleotide analogues. II. Synthesis of the adenyl analogue of Willardiine. Tetrahedron. 25: 5983-7. PMID 5377766 DOI: 10.1016/S0040-4020(01)83105-7 |
0.387 |
|
| 1969 |
Nollet AJ, Huting CM, Pandit UK. Unconventional nucleotide analogues. I. N9-purinyl alpha-amino acids. Tetrahedron. 25: 5971-81. PMID 5377765 DOI: 10.1016/S0040-4020(01)83104-5 |
0.373 |
|
| 1969 |
Nollet AJ, Pandit UK. Unconventional nucleotide analogues. 3. 4-(N1-pyrimidyl)-2-aminobutyric acids. Tetrahedron. 25: 5989-94. PMID 5373538 DOI: 10.1016/S0040-4020(01)83106-9 |
0.389 |
|
| 1969 |
Pandit UK, Pollmann MJM, Huisman HO. A simple synthesis of 6,7-diaza-steroids Journal of the Chemical Society D: Chemical Communications. 527. DOI: 10.1039/C29690000527 |
0.625 |
|
| 1969 |
Nollet AJH, Koomen GJ, Grose WFA, Pandit UK. Application of NMR spectroscopy in distinguishing between N1- and N3-substituted 2,4-dioxo-1,2,3,4,-tetrahydropyrimidines. Tetrahedron Letters. 10: 4607-4608. DOI: 10.1016/S0040-4039(01)88762-1 |
0.588 |
|
| 1969 |
Pandit UK, van der Vlugt FA, van Dalen AC. A new approach to the total synthesis of steroids Tetrahedron Letters. 10: 3697-3698. DOI: 10.1016/S0040-4039(01)88490-2 |
0.345 |
|
| 1969 |
Pandit UK, van der Vlugt FA, van Dalen AC, Joustra AH, Schenk H. A facile approach to ring C modified steroids Tetrahedron Letters. 10: 3693-3696. DOI: 10.1016/S0040-4039(01)88489-6 |
0.308 |
|
| 1969 |
Pandit UK, de Jonge K, Huisman HO. Heterocyclic steroids XV. Synthesis of 13,14-diazasteroidal systems Recueil Des Travaux Chimiques Des Pays-Bas. 88: 149-157. DOI: 10.1002/Recl.19690880204 |
0.389 |
|
| 1969 |
Pandit UK, de Jongen Mrs K, Erhart K, Huisman HO. A new approach to the total synthesis of B-norsteroids Tetrahedron Letters. 10: 1207-1208. |
0.579 |
|
| 1968 |
Speckamp WN, van Velthuysen JA, Douw MA, Pandit UK, Huisman HO. Heterocyclic steroids. 13. The synthesis of N-methyl-6-aza-8(14)-dehydro-19-nor-testosterone. Tetrahedron. 24: 5893-8. PMID 5713422 |
0.616 |
|
| 1968 |
Speckamp WN, van Velthuysen JA, Pandit UK, Huisman HO. Heterocyclic steroids. XII. N-ethyl-6-aza-8(14)-dehydroestrone methyl ether. Tetrahedron. 24: 5881-91. PMID 5713421 DOI: 10.1016/S0040-4020(01)96318-5 |
0.644 |
|
| 1967 |
Pandit UK, Jonge Kd, Koomen GJ, Huisman HO. Heterocyclic steroids IX : A Convenient Synthesis of 14-Aza-11-Keto Steroids☆ Tetrahedron Letters. 8: 3529-3533. DOI: 10.1016/S0040-4039(01)89836-1 |
0.455 |
|
| 1967 |
Pandit UK, Huisman HO. Heterocyclic steroids X. Synthesis of 12-aza-11-keto and 12-oxa-11-keto steroids Tetrahedron Letters. 8: 3901-3905. DOI: 10.1016/S0040-4039(01)89749-5 |
0.63 |
|
| 1967 |
Pandit UK, de Jonge K, Koomen GJ, Huisman HO. Heterocyclic steroids IX. A Convenient Synthesis of 14-Aza-11-Keto Steroids Tetrahedron Letters. 8: 3529-3533. |
0.746 |
|
| 1966 |
van Velthuysen JA, Douw MA, Speckamp WN, Pandit UK, Huisman HO. Heterocyclic steroids 8. Synthesis of (+ -)-N-methyl-6-aza-8(14)-dehydro-19-nor-testosterone. Tetrahedron Letters. 27: 3081-6. PMID 5955874 DOI: 10.1016/S0040-4039(01)99919-8 |
0.682 |
|
| 1966 |
Sluyter MA, Pandit UK, Speckamp WN, Huisman HO. Heterocyclic steroids. VI. Total synthesis of 4-aza-19-norsteroids. Tetrahedron Letters. 87-90. PMID 5904861 DOI: 10.1016/S0040-4039(01)99635-2 |
0.671 |
|
| 1966 |
Willems AGM, Eck RRv, Pandit UK, Huisman HO. Polynuclear heterocyclic systems IV A total synthesis of 11,12-diazasteroid skeleton. Tetrahedron Letters. 7: 81-86. DOI: 10.1016/S0040-4039(01)99634-0 |
0.625 |
|
| 1966 |
Westra JG, Speckamp WN, Pandit UK, Huisman HO. Heterocyclic steroids VII. Total synthesis of 6-thiasteroids Tetrahedron Letters. 7: 2781-2784. DOI: 10.1016/S0040-4039(00)62024-5 |
0.666 |
|
| 1966 |
Speckamp WN, Pandit UK, Korver PK, van der Haak PJ, Huisman HO. Dihydroquinolones-V. Hindered inversion in dihydroquinolones and related systems Tetrahedron. 22: 2413-2427. |
0.491 |
|
| 1965 |
Speckamp WN, de Koning H, Pandit UK, Huisman HO. Heterocyclic steroids. IV. Total synthesis of some 6-aza-estrogens. Tetrahedron. 21: 2517-27. PMID 5879296 DOI: 10.1016/S0040-4020(01)93907-9 |
0.65 |
|
| 1965 |
Pandit UK, Speckamp WN, Huisman HO. Heterocyclic steroids-III. Mass spectra of 6-azasteroids with two aromatic rings Tetrahedron. 21: 1767-1775. DOI: 10.1016/S0040-4020(01)98648-X |
0.616 |
|
| 1965 |
Gen Avd, Zunnebeld WA, Pandit UK, Huisman HO. Addition to steroid polyenes—III : Reactivity of the cholesta-5,7,9(11)-triene system Tetrahedron. 21: 3651-3659. DOI: 10.1016/S0040-4020(01)96980-7 |
0.347 |
|
| 1965 |
van der Gen A, Lakeman J, Pandit UK, Huisman HO. Addition to steroid polyenes-II. Reaction of 7-dehydrocholesteryl acetate with dimethyl acetylenedicarboxylate Tetrahedron. 21: 3641-3649. DOI: 10.1016/S0040-4020(01)96979-0 |
0.639 |
|
| 1965 |
van der Gen A, Zunnebeld WA, Pandit UK, Huisman HO. Addition to steroid polyenes-III. Reactivity of the cholesta-5,7,9(11)-triene system Tetrahedron. 21: 3651-3659. |
0.546 |
|
| 1964 |
Speckamp WN, Pandit UK, Huisman HO. A case of hindered inversion of trigonal nitrogen Tetrahedron Letters. 5: 3279-3284. DOI: 10.1016/S0040-4039(01)89423-5 |
0.545 |
|
| 1964 |
Huisman H, Speckamp W, de Koning H, Pandit U. Total synthesis of aza-steroids II Tetrahedron Letters. 5: 1275-1278. DOI: 10.1016/S0040-4039(00)90464-7 |
0.624 |
|
| 1964 |
Pandit U, Hofman H, Huisman H. Polynuclear heterocyclic systems—II Tetrahedron. 20: 1679-1684. DOI: 10.1016/S0040-4020(01)99167-7 |
0.586 |
|
| 1964 |
de Koning H, Wiedhaup K, Pandit UK, Huisman HO. A convenient synthesis of 9,10-dihydrophenanthrene-9-carboxylic acid Recueil Des Travaux Chimiques Des Pays-Bas. 83: 364-366. DOI: 10.1002/Recl.19640830405 |
0.306 |
|
| 1964 |
Pandit UK, Hofman HJ, Huisman HO. Polynuclear heterocyclic systems-II. Mass spectra of certain benzindole and dihydrobenzindole acids and esters Tetrahedron. 20: 1679-1684. |
0.542 |
|
| 1964 |
Huisman HO, Speckamp WN, de Koning H, Pandit UK. Total synthesis of aza-steroids II. Methyl ethers of 6-azaequilenin and 8ε{lunate},9ε{lunate}-6-azaestrone Tetrahedron Letters. 5: 1275-1278. |
0.599 |
|
| 1963 |
Heitman H, Pandit UK, Huisman HO. Some stereochemical implications of a bi-functional wittig reaction Tetrahedron Letters. 4: 915-920. DOI: 10.1016/S0040-4039(01)90743-9 |
0.603 |
|
| 1961 |
Pandit UK, Kloetzel MC. Synthetic analogs of cortical hormones. IV. Synthesis and reactions of 3-acetoxy-2-oxo-3-(2-phenanthryl)-diazopropane Journal of the American Chemical Society. 83: 482-486. DOI: 10.1021/Ja01463A053 |
0.683 |
|
| 1959 |
KLOETZEL MC, DAVIS SJ, PANDIT U, SMITH CR, NISHIHARA H. Potential chemotherapeutic compounds. III. Derivatives of 2-aminodiphenylamine and N,N-bis(4-aminophenyl)-alkylamines. Journal of Medicinal and Pharmaceutical Chemistry. 1: 197-211. PMID 14409941 DOI: 10.1021/Jm50004A001 |
0.647 |
|
| 1956 |
Kloetzel MC, Pandit UK. Synthetic analogs of cortical hormones. III. Hydroxymethyl 9,10-diacetoxyphenanthryl ketones Journal of the American Chemical Society. 78: 1412-1413. DOI: 10.1021/Ja01588A040 |
0.64 |
|
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