Year |
Citation |
Score |
2014 |
Jacobi PA, Mascall KC. Synthetic Studies on Furanosteroids. Functionalization of Ring A of the Viridin Core Skeleton Heterocycles. 88: 1527. DOI: 10.3987/Com-13-S(S)71 |
0.72 |
|
2013 |
Onyango EO, Jacobi PA. Synthesis of an advanced precursor of demethoxyviridin Synthetic Communications. 43: 2748-2755. DOI: 10.1080/00397911.2012.737078 |
0.756 |
|
2013 |
Jacobi PA, Könekamp T, Mascall KC, O'Connor RT, Onyango EO, Sessions EH. Constructing the Heterocyclic Core of Viridin and Wortmannin Advances in Heterocyclic Chemistry. 110: 119-143. DOI: 10.1016/B978-0-12-408100-0.00004-5 |
0.671 |
|
2012 |
Onyango EO, Jacobi PA. Synthetic studies on furanosteroids: construction of the viridin core structure via Diels-Alder/retro-Diels-Alder and vinylogous Mukaiyama aldol-type reaction. The Journal of Organic Chemistry. 77: 7411-27. PMID 22849426 DOI: 10.1021/Jo301232W |
0.742 |
|
2012 |
Mascall KC, Jacobi PA. Furanosteroid studies. Improved synthesis of the A,B,C,E-ring core of viridin Tetrahedron Letters. 53: 1620-1623. DOI: 10.1016/J.Tetlet.2012.01.070 |
0.747 |
|
2010 |
Wang H, Jacobi PA. An improved synthesis of a ring-C precursor to cobyric acid Arkivoc. 2010: 15-24. DOI: 10.3998/Ark.5550190.0011.403 |
0.476 |
|
2010 |
Jacobi PA, Brielmann HL, Chiu M, Ghosh I, Hauck SI, Lanz S, Leung S, Li Y, Liu H, Löwer F, O'Neal WG, Pippin D, Pollina E, Pratt BA, Robert F, et al. 4-alkynoic acids in the synthesis of biologically important tetrapyrroles Heterocycles. 82: 1029-1081. DOI: 10.3987/Rev-10-Sr(E)6 |
0.736 |
|
2009 |
Ben Dror S, Bronshtein I, Weitman H, Smith KM, O'Neal WG, Jacobi PA, Ehrenberg B. The binding of analogs of porphyrins and chlorins with elongated side chains to albumin. European Biophysics Journal : Ebj. 38: 847-55. PMID 19330323 DOI: 10.1007/S00249-009-0444-Y |
0.381 |
|
2008 |
Wang H, Tassa C, Jacobi PA. Toward the synthesis of cobyric acid. Enantioselective syntheses of completely differentiated ring D synthons. Organic Letters. 10: 2837-40. PMID 18537250 DOI: 10.1021/Ol800985M |
0.46 |
|
2008 |
O'Neal WG, Jacobi PA. Toward a general synthesis of chlorins. Journal of the American Chemical Society. 130: 1102-8. PMID 18166060 DOI: 10.1021/Ja0780075 |
0.431 |
|
2007 |
Sessions EH, O'Connor RT, Jacobi PA. Furanosteroid studies. Stereoselective synthesis of the A,B,E-ring core of wortmannin. Organic Letters. 9: 3221-4. PMID 17655248 DOI: 10.1021/ol071158s |
0.305 |
|
2006 |
O'Neal WG, Roberts WP, Ghosh I, Wang H, Jacobi PA. Studies in chlorin chemistry. 3. A practical synthesis of c,d-ring symmetric chlorins of potential utility in photodynamic therapy. The Journal of Organic Chemistry. 71: 3472-80. PMID 16626128 DOI: 10.1021/Jo060041Z |
0.625 |
|
2005 |
Jacobi PA, Adel Odeh IM, Buddhu SC, Cai G, Rajeswari S, Fry D, Zheng W, Desimone RW, Guo J, Coutts LD, Hauck SI, Leung SH, Ghosh I, Pippin D. Synthetic Studies in Phytochrome Chemistry. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2861-2885. PMID 18633455 DOI: 10.1055/S-2005-918956 |
0.712 |
|
2005 |
O'Neal WG, Roberts WP, Ghosh I, Jacobi PA. Studies in chlorin chemistry. II. A versatile synthesis of dihydrodipyrrins. The Journal of Organic Chemistry. 70: 7243-51. PMID 16122244 DOI: 10.1021/Jo050907L |
0.61 |
|
2004 |
Roberts WP, Ghosh I, Jacobi PA. RZnl vs. R2Zn in Pd(0)-catalyzed cross-coupling reactions with thioimidates Canadian Journal of Chemistry. 82: 279-284. DOI: 10.1139/V03-205 |
0.46 |
|
2003 |
Jacobi PA, Li Y. Enantioselective syntheses of ring-C precursors of vit. B(12). Reagent control. Organic Letters. 5: 701-4. PMID 12605494 DOI: 10.1021/Ol0275116 |
0.698 |
|
2002 |
Ghosh I, Jacobi PA. Lewis acid-promoted oxidative addition of thioimidates to Pd0. The Journal of Organic Chemistry. 67: 9304-9. PMID 12492332 DOI: 10.1021/jo026510o |
0.468 |
|
2001 |
Jacobi PA, Lanz S, Ghosh I, Leung SH, Löwer F, Pippin D. A new synthesis of chlorins. Organic Letters. 3: 831-4. PMID 11263893 DOI: 10.1021/Ol006983M |
0.597 |
|
2000 |
Jacobi PA, DeSimone RW, Ghosh I, Guo J, Leung SH, Pippin D. New syntheses of the C,D-ring pyrromethenones of phytochrome and phycocyanin. The Journal of Organic Chemistry. 65: 8478-89. PMID 11112567 DOI: 10.1021/jo005531k |
0.613 |
|
2000 |
Jacobi PA, Coutts LD, Guo J, Hauck SI, Leung SH. New strategies for the synthesis of biologically important tetrapyrroles. The "B,C + D + A" approach to linear tetrapyrroles. The Journal of Organic Chemistry. 65: 205-13. PMID 10813917 DOI: 10.1021/jo991503u |
0.312 |
|
1999 |
Jacobi PA, Liu H. Iterative synthesis of semicorrins, tripyrrolines, and higher analogues [3] Journal of the American Chemical Society. 121: 1958-1959. DOI: 10.1021/ja983698d |
0.357 |
|
1997 |
Jacobi PA, Herradura P. Enantioselective syntheses of (+)- and (-)-blastmycinolactol Tetrahedron Letters. 38: 6621-6624. DOI: 10.1016/S0040-4039(97)01533-5 |
0.321 |
|
1996 |
Jacobi PA, Brielmann HL, Hauck SI. Toward the synthesis of biologically important chlorins, isobacteriochlorins, and corrins. Cyclic enamides from acetylenic amides Journal of Organic Chemistry. 61: 5013-5023. DOI: 10.1021/jo960428+ |
0.351 |
|
1996 |
Jacobi PA, Guo J, Hauck SI, Leung SH. An improved synthesis of the C,D-ring pyrromethenone of phytochrome and phytochromobilin Tetrahedron Letters. 37: 6069-6072. DOI: 10.1016/0040-4039(96)01317-2 |
0.318 |
|
1995 |
Jacobi PA, Guo J, Zheng W. An unequivocal synthesis of the ring-A,B dihydropyrromethenone of phytochrome Tetrahedron Letters. 36: 1197-1200. DOI: 10.1016/0040-4039(95)00032-8 |
0.336 |
|
1995 |
Jacobi PA, Brielmann HL, Hauck SI. Synthesis of cyclic enamides by intramolecular cyclization of acetylenic amides Tetrahedron Letters. 36: 1193-1196. DOI: 10.1016/0040-4039(95)00031-7 |
0.403 |
|
1991 |
Jacobi PA, Zheng W. A novel synthesis of juncusol Tetrahedron Letters. 32: 1279-1282. DOI: 10.1016/S0040-4039(00)79645-6 |
0.372 |
|
1991 |
Jacobi PA, Cai G. 2-oxo-3-butenoate esters as dienophiles and their utility in a novel synthesis of pyrroles Tetrahedron Letters. 32: 1765-1768. DOI: 10.1016/S0040-4039(00)74324-3 |
0.396 |
|
1989 |
Jacobi PA, Blum CA, DeSimone RW, Udodong UES. Total synthesis of (+)- and (-)-norsecurinine Tetrahedron Letters. 30: 7173-7176. DOI: 10.1016/S0040-4039(01)93926-7 |
0.355 |
|
1988 |
Jacobi PA, Kravitz JI. Enynones in organic synthesis. III. A novel synthesis of phenols Tetrahedron Letters. 29: 6873-6876. DOI: 10.1016/S0040-4039(00)88463-4 |
0.309 |
|
1988 |
Jacobi PA, Armacost LM, Kravitz JI, Martinelli MJ, Selnick HG. Enynones in organic synthesis. I. Spiroannulation by tandem oxy-cope rearrangement-electrocyclic ring closure Tetrahedron Letters. 29: 6865-6868. DOI: 10.1016/S0040-4039(00)88461-0 |
0.33 |
|
1988 |
Jacobi PA, Buddhu SC. A novel synthesis of pyrromethenones Tetrahedron Letters. 29: 4823-4826. DOI: 10.1016/S0040-4039(00)80618-8 |
0.372 |
|
1981 |
Woodward RB, Logusch E, Nambiar KP, Sakan K, Ward DE, Au-Yeung BW, Balaram P, Browne LJ, Card PJ, Chen CH, Chênevert RB, Fliri A, Frobel K, Gais HJ, Garratt DG, ... ... Jacobi PA, et al. Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin Journal of the American Chemical Society. 103: 3215-3217. DOI: 10.1021/Ja00401A051 |
0.729 |
|
1981 |
Woodward RB, Logusch E, Nambiar KP, Sakan K, Ward DE, Au-Yeung BW, Balaram P, Browne LJ, Card PJ, Chen CH, Chênevert RB, Fliri A, Frobel K, Gais HJ, Garratt DG, ... ... Jacobi PA, et al. Asymmetric total synthesis of erythromycin. 1. Synthesis of an erythronolide A seco acid derivative via asymmetric induction Journal of the American Chemical Society. 103: 3210-3213. DOI: 10.1021/Ja00401A049 |
0.591 |
|
1981 |
Jacobi PA, Martinelli M, Taylor EC. Unequivocal synthesis of euglenapterin Journal of Organic Chemistry. 46: 5416-5418. |
0.372 |
|
1981 |
Woodward RB, Logusch E, Nambiar KP, Sakan K, Ward DE, Au-Yeung BW, Balaram P, Browne LJ, Card PJ, Chen CH, Chênevert RB, Fliri A, Frobel K, Gais HJ, Garratt DG, ... ... Jacobi PA, et al. Asymmetric total synthesis of erythromycin. 2. Synthesis of an erythronolide A lactone system Journal of the American Chemical Society. 103: 3213-3215. |
0.602 |
|
1976 |
Taylor EC, Jacobi PA. Pteridines. XXXVII. A total synthesis of L-erythro-biopterin and some related 6-(polyhydroxyalkyl)pterins. Journal of the American Chemical Society. 98: 2301-7. PMID 1254867 DOI: 10.1021/Ja00424A051 |
0.439 |
|
1975 |
Taylor EC, Abdulla RF, Tanaka K, Jacobi PA. Pteridines. XXXVI. Syntheses of xanthopterin and isoxanthopterin. Application of N-oxide chemistry to highly functionalized pyrazines and pteridines. The Journal of Organic Chemistry. 40: 2341-7. PMID 1177061 DOI: 10.1021/Jo00904A017 |
0.398 |
|
1975 |
Taylor EC, Jacobi PA. Pteridines. XXXIV. Synthesis of 8-hydroxy-7(8H)-pteridinones (Pteridine hydroxamic acids). The Journal of Organic Chemistry. 40: 2332-6. PMID 1177060 DOI: 10.1021/Jo00904A015 |
0.466 |
|
1975 |
TAYLOR EC, ABDULLA RF, JACOBI PA. ChemInform Abstract: PTERIDINES PART 35, TOTAL SYNTHESIS OF ASPEROPTERIN Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197548338 |
0.55 |
|
1974 |
Taylor EC, Jacobi PA. Letter: An unequivocal total synthesis of L-erythro-biopterin. Journal of the American Chemical Society. 96: 6781-2. PMID 4414114 DOI: 10.1021/Ja00828A052 |
0.447 |
|
1974 |
TAYLOR EC, JACOBI PA. ChemInform Abstract: PTERIDINES PART 33, AN UNEQUIVOCAL TOTAL SYNTHESIS OF L-ERYTHRO-BIOPTERIN Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197452311 |
0.461 |
|
1973 |
Taylor EC, Jacobi PA. Pteridines. XXX. A facile synthesis of xanthopterin. Journal of the American Chemical Society. 95: 4455-6. PMID 4708393 DOI: 10.1021/Ja00794A071 |
0.557 |
|
1973 |
TAYLOR EC, PERLMAN KL, KIM Y, SWORD IP, JACOBI PA. ChemInform Abstract: PTERIDINES PART 29, AN UNEQUIVOCAL ROUTE TO 2,4-DIAMINO-6-SUBSTITUTED PTERIDINES Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/chin.197347322 |
0.495 |
|
1973 |
TAYLOR EC, PERLMAN KL, SWORD IP, SEQUIN-FREY M, JACOBI PA. ChemInform Abstract: PTERIDINES PART 28, A NEW, GENERAL, AND UNEQUIVOCAL PTERIN SYNTHESIS Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/chin.197347321 |
0.507 |
|
1973 |
TAYLOR EC, JACOBI PA. ChemInform Abstract: PTERIDINES PART 30, A FACILE SYNTHESIS OF XANTHOPTERIN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/chin.197336395 |
0.558 |
|
Low-probability matches (unlikely to be authored by this person) |
1979 |
Jacobi PA, Ueng SN, Carr D. An unusually facile ring opening of 5-alkoxyoxazoles. Application to the synthesis of dimethoxy-α-methyldopa Journal of Organic Chemistry. 44: 2042-2044. |
0.299 |
|
2003 |
Jacobi PA, Tassa C. Enantioselective syntheses of ring-C precursors of vitamin B12. Substrate control. A novel Si-assisted elimination of vinyl bromides. Organic Letters. 5: 4879-82. PMID 14653697 DOI: 10.1021/ol036061u |
0.295 |
|
1988 |
Jacobi PA, Egbertson M, Frechette RF, Miao CK, Weiss KT. Thiazoles in organic synthesis. Novel syntheses of menthanes and eremophilanes Tetrahedron. 44: 3327-3338. DOI: 10.1016/S0040-4020(01)85966-4 |
0.293 |
|
2009 |
Dror SB, Bronshtein I, Garini Y, O'Neal WG, Jacobi PA, Ehrenberg B. The localization and photosensitization of modified chlorin photosensitizers in artificial membranes. Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society For Photobiology. 8: 354-61. PMID 19255676 DOI: 10.1039/B814970D |
0.293 |
|
1993 |
Jacobi PA, Zheng W. A versatile synthesis of β-amino acids using the nicholas reaction. II. Formal total synthesis of thienamycin. Tetrahedron Letters. 34: 2585-2588. DOI: 10.1016/S0040-4039(00)77631-3 |
0.288 |
|
1973 |
Taylor EC, Perlman KL, Sword IP, Sequin-Frey M, Jacobi PA. Pteridines. XXVIII. A new, general, and unequivocal pterin synthesis Journal of the American Chemical Society. 95: 6407-6412. |
0.284 |
|
1991 |
Jacobi PA, Blum CA, DeSimone RW, Udodong UES. Bis-heteroannulation. 15. Enantiospecific syntheses of (+)and (-)-norsecurinine Journal of the American Chemical Society. 113: 5384-5392. |
0.283 |
|
2001 |
Jacobi PA, Li Y. Synthesis of porphobilinogen via a novel ozonide cleavage reaction. Journal of the American Chemical Society. 123: 9307-12. PMID 11562213 DOI: 10.1021/Ja016303Q |
0.282 |
|
1992 |
Jacobi PA, Rajeswari S. Tetrapyrroles. IV. A highly efficient synthesis of homochiral dihydropyrromethenones via Pdo mediated coupling of iodopyrroles and acetylenic amides Tetrahedron Letters. 33: 6235-6238. DOI: 10.1016/S0040-4039(00)60941-3 |
0.282 |
|
1973 |
Taylor EC, Perlman KL, Kim YH, Sword IP, Jacobi PA. Pteridines. XXIX. An unequivocal route to 2,4-diamino-6-substituted pteridines Journal of the American Chemical Society. 95: 6413-6418. |
0.277 |
|
2006 |
Sessions EH, Jacobi PA. Studies on the synthesis of furanosteroids. I. Viridin models. Organic Letters. 8: 4125-8. PMID 16928090 DOI: 10.1021/ol061697h |
0.276 |
|
1992 |
Jacobi PA, Cann RO, Skibbie DF. A convenient synthesis of methylenomycin B. Further mechanistic studies on the SET catalyzed electrocyclization of enynones. Tetrahedron Letters. 33: 2265-2268. DOI: 10.1016/S0040-4039(00)74185-2 |
0.273 |
|
1993 |
Jacobi PA, Cai G. A convenient synthesis of pyrrole- and N-aminopyrrole-3-propionate esters Heterocycles. 35: 1103-1120. |
0.27 |
|
1994 |
Jacobi PA, Armacost LM, Brielmann HL, Cann RO, Kravitz JI, Martinelli MJ. Enynones in organic synthesis. 6. Synthesis of spirocyclic methylenecyclopentenones and analogs of the methylenomycin class of antibiotics. Mechanism of phenol catalysis Journal of Organic Chemistry. 59: 5292-5304. DOI: 10.1021/jo00097a035 |
0.258 |
|
1975 |
TAYLOR EC, JACOBI PA. ChemInform Abstract: PTERIDINES PART 34, SYNTHESIS OF 8-HYDROXY-7(8H)-PTERIDINONES(PTERIDINE HYDROXAMIC ACIDS) Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197548339 |
0.257 |
|
2010 |
JACOBI PA, ZHENG W. ChemInform Abstract: Enantioselective Synthesis of β-Amino Acids Using the Nicholas Reaction Cheminform. 28: no-no. DOI: 10.1002/chin.199746314 |
0.253 |
|
1975 |
Taylor EC, Abdulla RF, Jacobi PA. Pteridines. XXXV. Total synthesis of asperopterin B Journal of Organic Chemistry. 40: 2336-2340. |
0.253 |
|
1997 |
Jacobi PA, Guo J, Rajeswari S, Zheng W. Dihydropyrromethenones by Pd(0)-Mediated Coupling of Iodopyrroles and Acetylenic Amides. Synthesis of the A,B-Ring Segment of Phytochrome. The Journal of Organic Chemistry. 62: 2907-2916. PMID 11671654 |
0.249 |
|
1995 |
Jacobi PA, Kravitz JI, Zheng W. Enynones in organic synthesis. 8. Synthesis of the antimicrobial-cytotoxic agent juncusol and members of the effusol class of phenols Journal of Organic Chemistry. 60: 376-385. |
0.248 |
|
1997 |
Jacobi PA, Buddhu SC, Fry D, Rajeswari S. Studies on the Synthesis of Phytochrome and Related Tetrapyrroles. Dihydropyrromethenones by Photochemical Rearrangement of N-Pyrrolo Enamides. The Journal of Organic Chemistry. 62: 2894-2906. PMID 11671653 |
0.248 |
|
1994 |
Jacobi PA, Brielmann HL, Cann RO. Enynones in organic synthesis. 7. Substituent effects on the α-tocopherol-catalyzed cyclization of enynones to methylenecyclopentenones. Convenient syntheses of members of the methylenomycin class of antibiotics Journal of Organic Chemistry. 59: 5305-5316. |
0.239 |
|
2000 |
Jacobi PA, Liu H. On the mechanism of Pd(0)-initiated coupling-cyclization of gamma-aminoalkynes. The Journal of Organic Chemistry. 65: 7676-81. PMID 11076634 DOI: 10.1021/Jo005606K |
0.238 |
|
1999 |
Jacobi PA, Liu H. Synthesis of 1,2,3,7,8,9-hexahydrodipyrrins and secocorrins: important precursors for the construction of corrins. Organic Letters. 1: 341-4. PMID 10822573 |
0.237 |
|
1999 |
Jacobi PA, Liu H. Studies on Corrin Synthesis. A Solution to the Introduction of Meso Substituents. The Journal of Organic Chemistry. 64: 1778-1779. PMID 11674262 DOI: 10.1021/jo9824899 |
0.236 |
|
1992 |
Jacobi PA, DeSimone RW. Tetrapyrroles. V. Formal syntheses of the ring-C,D pyrromethenones of phytochrome and phycocyanin Tetrahedron Letters. 33: 6239-6242. DOI: 10.1016/S0040-4039(00)60942-5 |
0.234 |
|
1996 |
Jacobi PA, Herradura P. Enantioselective syntheses of (+)- and (-)-phaseolinic acid Tetrahedron Letters. 37: 8297-8300. DOI: 10.1016/0040-4039(96)01941-7 |
0.227 |
|
2001 |
Jacobi PA, Herradura P. Enantioselective syntheses of (+)- and (-)-nephrosteranic acid employing the Nicholas-Schreiber reaction Canadian Journal of Chemistry. 79: 1727-1735. DOI: 10.1139/cjc-79-11-1727 |
0.224 |
|
1978 |
Jacobi PA, Craig T. Bis heteroannulation. 1. Model studies in the synthesis of highly oxygenated sesquiterpenes [17] Journal of the American Chemical Society. 100: 7748-7750. |
0.221 |
|
2001 |
Jacobi PA, Pippin D. Enantioselective syntheses of (13)C-labeled (2R)- and (2S)-phytochromobilin dimethyl ester. Organic Letters. 3: 827-30. PMID 11263892 DOI: 10.1021/ol006977q |
0.217 |
|
1995 |
Jacobi PA, Guo J. A conceptually new approach to the synthesis of linear tetrapyrroles related to phytochrome Tetrahedron Letters. 36: 2717-2720. DOI: 10.1016/0040-4039(95)00376-N |
0.208 |
|
1988 |
Jacobi PA, Armacost LM, Kravitz JI, Martinelli MJ. Enynones in organic synthesis. II. An electron transfer mediated synthesis of methylenecyclopentenones Tetrahedron Letters. 29: 6869-6872. DOI: 10.1016/S0040-4039(00)88462-2 |
0.207 |
|
1981 |
Jacobi PA, Brownstein A, Martinelli M, Grozinger K. A mild procedure for the generation of azomethine imines. Stereochemical factors in the intramolecular 1,3-dipolar addition of azomethine imines and a synthetic approach to saxitoxin Journal of the American Chemical Society. 103: 239-241. |
0.186 |
|
1984 |
JACOBI PA, WEISS KT, EGBERTSON M. ChemInform Abstract: BISHETEROANNULATION. 6. THE FIRST EXAMPLE OF A DIELS-ALDER REACTION INVOLVING G A THIAZOLE RING WITH AN ACETYLENIC DIENOPHILE. GEOMETRICAL CONTROL OF REACTION PATHWAY Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198429086 |
0.184 |
|
2010 |
JACOBI PA, TOUCHETTE KM, SELNICK HG. ChemInform Abstract: Bis-Heteroannulation. Part 16. A Synthetic Approach to Geigerin. Cheminform. 24: no-no. DOI: 10.1002/chin.199311256 |
0.18 |
|
1981 |
Jacobi PA, Walker DG, Odeh IMA. Bis heteroannulation. 2. Oxazole alcohols from the interaction of lithiomethyl isocyanide with lactones. A novel synthesis of evodone Journal of Organic Chemistry. 46: 2065-2069. |
0.174 |
|
1993 |
Jacobi PA, Zheng W. A versatile, synthesis of β-amino acids using the Nicholas reaction. I. Application to β-lactams of the carbapenem class Tetrahedron Letters. 34: 2581-2584. DOI: 10.1016/S0040-4039(00)77630-1 |
0.173 |
|
1984 |
Jacobi PA, Kaczmarek CSR, Udodong UE. Bis heteroannulation. 8. Total synthesis of (±)-paniculide-A Tetrahedron Letters. 25: 4859-4862. DOI: 10.1016/S0040-4039(01)91243-2 |
0.167 |
|
2018 |
Jacobi P. A Tribute to Prof. Gordon Gribble Arkivoc. 2018: 1-5. DOI: 10.24820/Ark.5550190.P001.473 |
0.159 |
|
1984 |
Jacobi PA, Martinelli MJ, Polanc S. Total synthesis of (±)-saxitoxin Journal of the American Chemical Society. 106: 5594-5598. |
0.147 |
|
1997 |
Jacobi PA, Lee K. Total synthesis of (±)-stemoamide Journal of the American Chemical Society. 119: 3409-3410. DOI: 10.1021/ja9642727 |
0.146 |
|
1987 |
Jacobi PA, Kaczmarek CSR, Udodong UE. Total synthesis of (±)-paniculide-a Tetrahedron. 43: 5475-5488. DOI: 10.1016/S0040-4020(01)87731-0 |
0.146 |
|
1992 |
Jacobi PA, Touchette KM, Selnick HG. Bis-heteroannulation. 16. A synthetic approach to geigerin Journal of Organic Chemistry. 57: 6305-6313. |
0.142 |
|
1984 |
Jacobi PA, Craig TA, Walker DG, Arrick BA, Frechette RF. Bis heteroannulation. 4. Facile syntheses of methylene acids, methylbutenolides, α-methyl-γ-lactones, and related materials. Total syntheses of (±)-ligularone and (±)-petasalbine Journal of the American Chemical Society. 106: 5585-5594. |
0.141 |
|
1993 |
Jacobi PA, Martin SF. A perspective on the contributions to heterocyclic chemistry by Professor Edward C. Taylor of Princeton University Heterocycles. 35: 1-31. |
0.122 |
|
1996 |
Jacobi PA, Murphree S, Rupprecht F, Zheng W. Formal total syntheses of the β-lactam antibiotics thienamycin and PS-5 Journal of Organic Chemistry. 61: 2413-2427. DOI: 10.1021/jo952092u |
0.107 |
|
2003 |
Jacobi PA, Sessions EH. On the methylation of carboxyl groups with methanesulfonyl chloride in pyridine Synthetic Communications. 33: 2575-2579. DOI: 10.1081/SCC-120021975 |
0.102 |
|
1992 |
Jacobi PA, Rajeswari S. Tetrapyrroles. III. Homochiral dihydropyrromethenones from N-Aminopyrroles and acetylenic acids Tetrahedron Letters. 33: 6231-6234. DOI: 10.1016/S0040-4039(00)60940-1 |
0.096 |
|
1990 |
Jacobi PA, Selnick HG. Total synthesis of (±)-gnididione and (±)-isognididione Journal of Organic Chemistry. 55: 202-209. |
0.077 |
|
2000 |
Jacobi PA, Lee K. Total syntheses of (±) and (-)-stemoamide Journal of the American Chemical Society. 122: 4295-4303. DOI: 10.1021/ja994214w |
0.064 |
|
1981 |
Jacobi PA, Walker DG. Bis heteroannulation. 3. Facile syntheses of (±)-ligularone and (±)-petasalbine Journal of the American Chemical Society. 103: 4611-4613. |
0.048 |
|
1987 |
Jacobi PA, Frechette RF. Stereospecific total syntheses of 7α- and 7β-eremophilane-6-one and 7α- and 7β-eremophilane Tetrahedron Letters. 28: 2937-2940. DOI: 10.1016/S0040-4039(00)96248-8 |
0.045 |
|
1984 |
Jacobi PA, Selnick HG. Bis heteroannulation. 7. Total syntheses of (±)-gnididione and (±)-isognididione Journal of the American Chemical Society. 106: 3041-3043. |
0.044 |
|
Hide low-probability matches. |