| Year |
Citation |
Score |
| 2012 |
Romero AL, Baptistella LHB, Coelho F, Imamura PM. Resolução do ibuprofeno: um projeto para disciplina de química orgânica experimental QuíMica Nova. 35: 1680-1685. DOI: 10.1590/S0100-40422012000800031 |
0.35 |
|
| 2009 |
Romero AL, Baptistella LHB, Imamura PM. Absolute configuration of some dinorlabdanes from the copaiba oil Journal of the Brazilian Chemical Society. 20: 1036-1040. DOI: 10.1590/S0103-50532009000600006 |
0.314 |
|
| 2008 |
de Carvalho MS, Baptistella LH, Imamura PM. 13C and 1H NMR signal assignments of some new synthetic dehydroabietic acid derivatives. Magnetic Resonance in Chemistry : Mrc. 46: 381-6. PMID 18273874 DOI: 10.1002/Mrc.2187 |
0.329 |
|
| 2006 |
Ide RM, Costa M, Imamura PM. Synthesis of Ent-16-hydroxycleroda-4(18),13-dien-15,16-olide and Ent-cleroda-4(18),13-dien-15,16-olide from (+)-hardwickiic acid Journal of the Brazilian Chemical Society. 17: 417-420. DOI: 10.1590/S0103-50532006000200029 |
0.462 |
|
| 2005 |
Imamura PM, Santos Cd. Synthesis of an Oidiolactone Analogue from Abietic Acid Synthetic Communications. 35: 2057-2065. DOI: 10.1081/Scc-200066683 |
0.451 |
|
| 2004 |
Imamura PM, Miranda PC, Giacomini RA. A complete 1H and 13C NMR data assignment for the diterpene methyl (-)-zanzibarate by 2D spectroscopy and NOE experiments. Magnetic Resonance in Chemistry : Mrc. 42: 561-3. PMID 15137049 DOI: 10.1002/Mrc.1379 |
0.328 |
|
| 2003 |
Giacomini RA, Miranda PCMdL, Baptistella LHB, Imamura PM. Synthesis of ambergris odorant ent-ambrox Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.A29 |
0.338 |
|
| 2003 |
Santos Cd, Zukerman-Schpector J, Imamura PM. Chemical transformation of abietic acid to new chiral derivatives Journal of the Brazilian Chemical Society. 14: 998-1004. DOI: 10.1590/S0103-50532003000600017 |
0.438 |
|
| 2003 |
Baptistella LHB, Giacomini RA, Imamura PM. Síntese dos analgésicos paracetamol e fenacetina e do adoçante dulcina: um projeto para química orgânica experimental QuíMica Nova. 26: 284-286. DOI: 10.1590/S0100-40422003000200024 |
0.315 |
|
| 2002 |
Nogueira RT, Giacomini RA, Shepherd GJ, Imamura PM. A New ent-Clerodane Diterpene from Hymenaea courbaril var. altissima Journal of the Brazilian Chemical Society. 13: 389-391. DOI: 10.1590/S0103-50532002000300015 |
0.357 |
|
| 2002 |
Imamura PM, Costa M, Custódio R. A Convenient Preparation Of 1,2,3,4,5,6,7,8-Octahydro-Naphthalene Skeleton. Synthesis Of (±)-Isocaridiene Synthetic Communications. 32: 1393-1399. DOI: 10.1081/Scc-120003636 |
0.374 |
|
| 2002 |
Lunardi I, Santiago GMP, Imamura PM. Synthesis of (−)- and (+)-hyrtiosal and their C-16 epimers Tetrahedron Letters. 43: 3609-3611. DOI: 10.1016/S0040-4039(02)00576-2 |
0.425 |
|
| 2001 |
Nogueira RT, Shepherd GJ, Laverde A, Marsaioli AJ, Imamura PM. Clerodane-type diterpenes from the seed pods of Hymenaea courbaril var. stilbocarpa Phytochemistry. 58: 1153-1157. PMID 11738399 DOI: 10.1016/S0031-9422(01)00303-X |
0.351 |
|
| 2000 |
Imamura PM, Costa M. Synthesis of 16,18-dihydroxycleroda-3,13Z-dien-16,15-olide, (+)-16-hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-hydroxyhalima-5(10),13-dien-16,15-olide from (+)-hardwickiic acid. Journal of Natural Products. 63: 1623-1625. PMID 11141101 DOI: 10.1021/Np000105F |
0.364 |
|
| 2000 |
Costa M, Perles EC, Fujiwara FY, Imamura PM. Synthesis of methyl dihydrohardwickiate and its C-4 epimer. Structural amendment of natural crolechinic acid. Phytochemistry. 53: 851-854. PMID 10820791 DOI: 10.1016/S0031-9422(99)00583-X |
0.432 |
|
| 2000 |
Hess SC, Farah MIS, Eguchib SY, Imamura PM. Synthetic studies with Pinus elliottiis rosin derivatives. Oxidation of maleopimaric anhydride methyl ester and trimethyl fumaropimarate Journal of the Brazilian Chemical Society. 11: 59-63. DOI: 10.1590/S0103-50532000000100011 |
0.408 |
|
| 1999 |
Santos Cd, Rosso CRSd, Imamura PM. Synthesis Of New Chiral Synthons Through Regioselective Ozonolysis Of Methyl Abietate Synthetic Communications. 29: 1903-1910. DOI: 10.1080/00397919908086178 |
0.478 |
|
| 1999 |
Costa M, Tanaka CMA, Imamura PM, Marsaioli AJ. Isolation and synthesis of a new clerodane from Echinodorus grandiflorus Phytochemistry. 50: 117-122. DOI: 10.1016/S0031-9422(98)00464-6 |
0.374 |
|
| 1998 |
Costa M, Fujiwara FY, Imamura PM. Assignment of 13C NMR data of methyl (+)-hardwickiate and its derivatives Magnetic Resonance in Chemistry. 36: 542-544. DOI: 10.1002/(Sici)1097-458X(199807)36:7<542::Aid-Omr334>3.0.Co;2-7 |
0.36 |
|
| 1997 |
Imamura PM, Santiago GMP. Chlorosulfonic Acid Mediated Cyclization of Homoterpenic Acid Synthetic Communications. 27: 2479-2485. DOI: 10.1080/00397919708004111 |
0.322 |
|
| 1995 |
Imamura PM, Nogueira RT. A Convenient Synthesis of C-8 Oxo-eudesmane. Total Synthesis of (±)-Eudesma-5,7(11)-dien-8-one Synthetic Communications. 25: 405-412. DOI: 10.1080/00397919508011372 |
0.367 |
|
| 1995 |
Imamura PM, Pantarotto H. Total synthesis of ent‐α‐polypodatetraene Liebigs Annalen. 1995: 1891-1894. DOI: 10.1002/Jlac.1995199510265 |
0.464 |
|
| 1986 |
Leite MAF, Sarragiotto MH, Imamura PM, Marsaioli AJ. Absolute configuration of drim-9(11)-en-8-ol from Aspergillus oryzae Journal of Organic Chemistry. 51: 5409-5410. DOI: 10.1021/Jo00376A066 |
0.33 |
|
| 1981 |
Imamura PM, Sierra MG, Rúveda EA. Stereoselective synthesis of the noval marine diterpene (+)-isoagatholactone Journal of the Chemical Society, Chemical Communications. 734-735. DOI: 10.1039/C39810000734 |
0.66 |
|
| 1981 |
De Miranda DS, Brendolan G, Imamura PM, Sierra MG, Marsaioli AJ, Rúveda EA. Stereoselective synthesis of the enantiomer of the novel marine diterpene isoagatholactone, ent-13(16),14-spongiadien-12α-ol, and the parent hydrocarbon isocopalane from methyl isocopalate Journal of Organic Chemistry. 46: 4851-4858. DOI: 10.1021/Jo00337A006 |
0.628 |
|
| 1981 |
Imamura PM, Sierra MG, Ruveda EA. Stereoselective Synthesis Of The Novel Marine Diterpene (+)-Isoagatholactone Cheminform. 12. DOI: 10.1002/Chin.198150310 |
0.649 |
|
| 1980 |
Imamura PM, Ruveda EA. The C-13 configuration of the bromine-containing diterpene isoaplysin-20. Synthesis of debromoisoaplysin-20 and C-13 epimer Journal of Organic Chemistry. 11: 510-515. DOI: 10.1021/Jo01291A028 |
0.346 |
|
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