| Year |
Citation |
Score |
| 2010 |
IRELAND RE, LIU L, ROPER TD, GLEASON JL. ChemInform Abstract: Total Synthesis of FK-506. Part 2. Completion of the Synthesis. Cheminform. 29: no-no. DOI: 10.1002/chin.199805232 |
0.806 |
|
| 2010 |
IRELAND RE, LIU L, ROPER TD. ChemInform Abstract: Total Synthesis of FK-506. Part 1. Construction of the C16-C34 Fragment (I). Cheminform. 29: no-no. DOI: 10.1002/chin.199805231 |
0.729 |
|
| 2010 |
IRELAND RE, GLEASON JL, GEGNAS LD, HIGHSMITH TK. ChemInform Abstract: A Total Synthesis of FK-506. Cheminform. 28: no-no. DOI: 10.1002/chin.199705297 |
0.486 |
|
| 2010 |
IRELAND RE, MEISSNER RS, RIZZACASA MA. ChemInform Abstract: Convergent Synthesis of Polyether Ionophore Antibiotics: Protective Manipulation and Synthesis of Monensin A. Cheminform. 24: no-no. DOI: 10.1002/chin.199350306 |
0.707 |
|
| 2010 |
IRELAND RE, ARMSTRONG JDI, LEBRETON J, MEISSNER RS, RIZZACASA MA. ChemInform Abstract: Convergent Synthesis of Polyether Ionophore Antibiotics: Synthesis of the Spiroketal and Tricyclic Glycal Segments of Monensin. Cheminform. 24: no-no. DOI: 10.1002/chin.199350305 |
0.688 |
|
| 2010 |
IRELAND RE, WIPF P, XIANG J. ChemInform Abstract: Stereochemical Control in the Ester Enolate Claisen Rearrangement. Part 2. Chairlike vs Boatlike Transition-State Selection. Cheminform. 22: no-no. DOI: 10.1002/chin.199141054 |
0.359 |
|
| 2010 |
IRELAND RE, WIPF P, ARMSTRONG JDI. ChemInform Abstract: Stereochemical Control in the Ester Enolate Claisen Rearrangement. Part 1. Stereoselectivity in Silyl Ketene Acetal Formation. Cheminform. 22: no-no. DOI: 10.1002/chin.199131227 |
0.473 |
|
| 2003 |
Ireland RE, Walba DM. Demethylation of Methyl Aryl Ethers: 4‐Ethoxy‐3‐Hydroxybenzaldehyde Organic Syntheses. 44-44. DOI: 10.1002/0471264180.Os056.11 |
0.548 |
|
| 2003 |
Ireland RE, Dawson DJ. Ethyl 5β‐Cholest‐3‐ene‐5‐Acetate Organic Syntheses. 74-74. DOI: 10.1002/0471264180.Os054.16 |
0.329 |
|
| 2003 |
Ireland RE, Dawson DJ. 5β‐Cholest‐3‐ene‐5‐Acetaldehyde Organic Syntheses. 71-71. DOI: 10.1002/0471264180.Os054.15 |
0.306 |
|
| 2003 |
Trust RI, Ireland RE. Stereoselective Synthesis of Trisubstituted Olefins: Ethyl 4‐Methyl‐(E)‐4,8‐Nonadienoate Organic Syntheses. 116-116. DOI: 10.1002/0471264180.Os053.27 |
0.378 |
|
| 1997 |
Ireland RE, Liu L, Roper TD, Gleason JL. Total synthesis of FK-506. Part 2: Completion of the synthesis Tetrahedron. 53: 13257-13284. DOI: 10.1016/S0040-4020(97)00866-1 |
0.772 |
|
| 1997 |
Ireland RE, Liu L, Roper TD. Total synthesis of FK-506. Part 1: Construction of the C16-C34 fragment Tetrahedron. 53: 13221-13256. DOI: 10.1016/S0040-4020(97)00865-X |
0.723 |
|
| 1996 |
Ireland RE, Gleason JL, Gegnas LD, Highsmith TK. A Total Synthesis of FK-506(1). The Journal of Organic Chemistry. 61: 6856-6872. PMID 11667580 DOI: 10.1021/Jo951646Q |
0.66 |
|
| 1996 |
Ireland RE, Gleason JL, Gegnas LD, Highsmith TK. A total synthesis of FK-5061 Journal of Organic Chemistry. 61: 6856-6872. |
0.487 |
|
| 1993 |
Ireland RE, Meissner RS, Rizzacasa MA. Convergent synthesis of polyether ionophore antibiotics: Protective manipulation and synthesis of monensin A Journal of the American Chemical Society. 115: 7166-7172. DOI: 10.1021/Ja00069A014 |
0.718 |
|
| 1993 |
Ireland RE, Armstrong JD, Lebreton J, Meissner RS, Rizzacasa MA. Convergent synthesis of polyether ionophore antibiotics: Synthesis of the spiroketal and tricyclic glycal segments of monensin Journal of the American Chemical Society. 115: 7152-7165. DOI: 10.1021/Ja00069A013 |
0.685 |
|
| 1992 |
Ireland RE, Highsmith TK, Gegnas LD, Gleason JL. Synthesis of the 9,10-acetonide of 9-dihydro-FK-506 Journal of Organic Chemistry. 57: 5071-5073. DOI: 10.1021/Jo00045A013 |
0.701 |
|
| 1991 |
Ireland RE, Wipf P, Xiang JN. Stereochemical control in the ester enolate Claisen rearrangement. 2. Chairlike vs boatlike transition-state selection Journal of Organic Chemistry. 56: 3572-3582. DOI: 10.1021/Jo00011A023 |
0.446 |
|
| 1991 |
Ireland RE, Wipf P, Armstrong JD. Stereochemical control in the ester enolate Claisen rearrangement. 1. Stereoselectivity in silyl ketene acetal formation Journal of Organic Chemistry. 56: 650-657. DOI: 10.1021/Jo00002A030 |
0.524 |
|
| 1990 |
Ireland RE, Wipf P, Roper TD. Use of a masked aldol unit in the synthesis of the right side of FK-506 Journal of Organic Chemistry. 55: 2284-2285. DOI: 10.1021/Jo00295A009 |
0.771 |
|
| 1990 |
Ireland RE, Wipf P. Carboalumination of 1-alkynes and in situ transmetalation to higher order cyanocuprates. Stereospecific synthesis of tri- and disubstituted olefins by conjugate addition to enones Journal of Organic Chemistry. 55: 1425-1426. DOI: 10.1021/Jo00292A009 |
0.57 |
|
| 1990 |
Ireland RE, Wipf P, Miltz W, Vanasse B. Methodology for the enantioselective synthesis of aldols and other 1,3-dioxygenated systems Journal of Organic Chemistry. 55: 1423-1424. DOI: 10.1021/Jo00292A008 |
0.6 |
|
| 1990 |
IRELAND RE, WIPF P, MILTZ W, VANASSE B. ChemInform Abstract: Methodology for the Enantioselective Synthesis of Aldols and Other 1,3-Dioxygenated Systems. Cheminform. 21. DOI: 10.1002/chin.199033189 |
0.513 |
|
| 1990 |
IRELAND RE, WIPF P. ChemInform Abstract: Carboalumination of 1-Alkynes and in situ Transmetalation to Higher Order Cyanocuprates. Stereospecific Synthesis of Tri- and Disubstituted Olefins by Conjugate Addition to Enones. Cheminform. 21. DOI: 10.1002/chin.199033063 |
0.562 |
|
| 1989 |
Ireland RE, Wipf P. Studies directed towards the total synthesis of FK-506 preparation of a C(1) to C(15) segment Tetrahedron Letters. 30: 919-922. DOI: 10.1016/S0040-4039(00)95278-X |
0.458 |
|
| 1989 |
IRELAND RE, JEFFERSON T. ChemInform Abstract: Synthetic Methodology in the Context of Natural Product Total Synthesis Cheminform. 20. DOI: 10.1002/chin.198928362 |
0.355 |
|
| 1988 |
Ireland RE, Maienfisch P. The convergent synthesis of polyether ionophore antibiotics: The synthesis of the A ring carbamonensin spiro ether Journal of Organic Chemistry. 53: 640-651. DOI: 10.1021/Jo00238A030 |
0.529 |
|
| 1988 |
Ireland RE, Thaisrivongs S, Dussault PH. An approach to the total synthesis of aplysiatoxin Journal of the American Chemical Society. 110: 5768-5779. DOI: 10.1021/Ja00225A031 |
0.634 |
|
| 1988 |
Ireland RE, Smith MG. 3-Acyltetramic acid antibiotics. 2. Synthesis of (+)-streptolic acid Journal of the American Chemical Society. 110: 854-860. DOI: 10.1021/Ja00211A025 |
0.37 |
|
| 1988 |
IRELAND RE, THAISRIVONGS S, DUSSAULT PH. ChemInform Abstract: An Approach to the Total Synthesis of Aplysiatoxin. Cheminform. 19. DOI: 10.1002/chin.198850302 |
0.649 |
|
| 1988 |
IRELAND RE, MAIENFISCH P. ChemInform Abstract: The Convergent Synthesis of Polyether Ionophore Antibiotics: The Synthesis of the A Ring Carbamonensin Spiro Ether. Cheminform. 19. DOI: 10.1002/chin.198825368 |
0.449 |
|
| 1987 |
Ireland RE, Wardle RB. 3-Acyltetramic acid antibiotics. 3. An approach to the synthesis of Bu-2313 Journal of Organic Chemistry. 52: 1780-1789. DOI: 10.1021/Jo00385A024 |
0.419 |
|
| 1987 |
IRELAND RE, WARDLE RB. ChemInform Abstract: 3-Acyltetramic Acid Antibiotics. Part 3. An Approach to the Synthesis of Bu-2313. Cheminform. 18. DOI: 10.1002/chin.198741378 |
0.333 |
|
| 1986 |
Ireland RE, Varney MD. Approach to the total synthesis of chlorothricolide: Synthesis of (±)-19,20-dihydro-24-O-methylchlorothricolide, methyl ester, ethyl carbonate Journal of Organic Chemistry. 51: 635-648. DOI: 10.1021/Jo00355A013 |
0.447 |
|
| 1986 |
Ireland RE, Obrecht DM. Diels-Alder Approach to Highly Functionalized Tertiary ?-Hydroxy Ketones: A Novel Route to the Hexahydrobenzofuran Portion of the Avermectins and Milbemycins Helvetica Chimica Acta. 69: 1273-1286. DOI: 10.1002/Chin.198652126 |
0.354 |
|
| 1986 |
IRELAND RE, VARNEY MD. ChemInform Abstract: Approach to the Total Synthesis of Chlorothricolide: Synthesis of (±)-19,20-Dihy- dro-24-O-methylchlorothricolide, Methyl Ester, Ethyl Carbonate. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198636328 |
0.32 |
|
| 1985 |
Ireland RE, Norbeck DW, Mandel GS, Mandel NS. The convergent synthesis of polyether ionophore antibiotics: An approach to the synthesis of the monensin tetrahydropyran-bis(tetrahydrofuran) via the ester enolate Claisen rearrangement and reductive decarboxylation Journal of the American Chemical Society. 107: 3285-3294. DOI: 10.1021/Ja00297A039 |
0.555 |
|
| 1985 |
Ireland RE, Norbeck DW. The convergent synthesis of polyether ionophore antibiotics: The synthesis of the monensin bis(tetrahydrofuran) via the Claisen rearrangement of an ester enolate with a β-leaving group Journal of the American Chemical Society. 107: 3279-3285. DOI: 10.1021/Ja00297A038 |
0.498 |
|
| 1985 |
IRELAND RE, NORBECK DW. ChemInform Abstract: CONVERGENT SYNTHESIS OF POLYETHER IONOPHORE ANTIBIOTICS: THE SYNTHESIS OF THE MONENSIN BIS(TETRAHYDROFURAN) VIA THE CLAISEN REARRANGEMENT OF AN ESTER ENOLATE WITH A β-LEAVING GROUP Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198538344 |
0.41 |
|
| 1985 |
Ireland RE, Häbich D, Norbeck DW. The convergent synthesis of polyether ionophore antibiotics: The synthesis of the monensin spiroketal Journal of the American Chemical Society. 107: 3271-3278. DOI: 10.1002/Chin.198538343 |
0.546 |
|
| 1985 |
IRELAND RE, HAEBICH D, NORBECK DW. ChemInform Abstract: CONVERGENT SYNTHESIS OF POLYETHER IONOPHORE ANTIBIOTICS: THE SYNTHESIS OF THE MONENSIN SPIROKETAL Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198538343 |
0.469 |
|
| 1984 |
Ireland RE, Dow WC, Godfrey JD, Thaisrivongs S. Total synthesis of (.+-.)-aphidicolin and (.+-.)-.beta.-chamigrene The Journal of Organic Chemistry. 49: 1001-1013. DOI: 10.1021/Jo00180A010 |
0.325 |
|
| 1984 |
IRELAND RE, DOW WC, GODFREY JD, THAISRIVONGS S. ChemInform Abstract: TOTAL SYNTHESIS OF (.+-.)-APHIDICOLIN AND (.+-.)-β-CHAMIGRENE Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198435317 |
0.417 |
|
| 1984 |
IRELAND RE, COURTNEY L, FITZSIMMONS BJ. ChemInform Abstract: TOTAL SYNTHESIS OF POLYETHER ANTIBIOTICS. SYNTHESIS OF THE ENANTIOMER OF LASALOCID A (X-537A) Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198423319 |
0.342 |
|
| 1983 |
Ireland RE, Varney MD. Stereochemistry of the Claisen rearrangement of derivatives of 5-tert-butyl-1-(hydroxymethyl)-1-cyclohexene: Preferred axial attachment of the side chain Journal of Organic Chemistry. 48: 1829-1833. DOI: 10.1021/Jo00159A008 |
0.301 |
|
| 1983 |
Ireland RE, Daub JP, Mandel GS, Mandel NS. Macrolide total synthesis. The synthesis of seco-acid derivatives for the synthesis of methymycin and 10-deoxymethymycin Journal of Organic Chemistry. 48: 1312-1325. DOI: 10.1021/Jo00156A032 |
0.564 |
|
| 1983 |
Ireland RE, Daub JP. Macrolide total synthesis. The synthesis of spiro ketal intermediates and their cleavage into open-chain derivatives Journal of Organic Chemistry. 48: 1303-1312. DOI: 10.1021/Jo00156A031 |
0.533 |
|
| 1983 |
Ireland RE, Anderson RC, Badoud R, Fitzsimmons BJ, McGarvey GJ, Thaisrivongs S, Wilcox CS. The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A) Journal of the American Chemical Society. 105: 1988-2006. DOI: 10.1021/Ja00345A055 |
0.734 |
|
| 1983 |
Ireland RE, Courtney L, Fitzsimmons BJ. Total synthesis of polyether antibiotics. Synthesis of the enantiomer of lasalocid a (X-537A) Journal of Organic Chemistry. 48: 5186-5198. DOI: 10.1002/Chin.198423319 |
0.434 |
|
| 1983 |
IRELAND RE, DAUB JP, MANDEL GS, MANDEL NS. ChemInform Abstract: MACROLIDE TOTAL SYNTHESIS. THE SYNTHESIS OF SECO-ACID DERIVATIVES FOR THE SYNTHESIS OF METHYMYCIN AND 10-DEOXYMETHYMYCIN Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198337343 |
0.491 |
|
| 1983 |
IRELAND RE, ANDERSON RC, BADOUD R, FITZSIMMONS BJ, MCGARVEY GJ, THAISRIVONGS S, WILCOX CS. ChemInform Abstract: THE TOTAL SYNTHESIS OF IONOPHORE ANTIBIOTICS. A CONVERGENT SYNTHESIS OF LASALOCID A (X537A) Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198328370 |
0.717 |
|
| 1983 |
IRELAND RE, DAUB JP. ChemInform Abstract: SYNTHESIS OF CHIRAL SUBUNITS FOR MACROLIDE SYNTHESIS: AN EFFICIENT METHOD FOR CONVERTING SPIROKETALS INTO OPEN-CHAIN DERIVATIVES Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198301160 |
0.416 |
|
| 1982 |
Ireland RE, Daub JP. Synthesis of chiral subunits for macrolide synthesis: an efficient method for converting spiroketals into open-chain derivatives Tetrahedron Letters. 23: 3471-3474. DOI: 10.1016/S0040-4039(00)87644-3 |
0.453 |
|
| 1982 |
IRELAND RE, THOMPSON WJ, SROUJI GH, ETTER R. ChemInform Abstract: APPROACH TO THE TOTAL SYNTHESIS OF CHLOROTHRICOLIDE: SYNTHESIS OF “7-EPI-BOTTOM HALF” AND ITS UNION WITH “TOP HALF” SYSTEMS Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198216350 |
0.402 |
|
| 1981 |
Ireland RE, Vevert J. Synthèse totale des acides (+) et (–) nonactique à partir de carbohydrates Canadian Journal of Chemistry. 59: 572-583. DOI: 10.1139/V81-083 |
0.456 |
|
| 1981 |
Ireland RE, Thompson WJ, Srouji GH, Etter R. Approach to the total synthesis of chlorothricolide: Synthesis of "7-epi-bottom half" and its union with "top half" systems Journal of Organic Chemistry. 46: 4863-4873. DOI: 10.1021/Jo00337A008 |
0.483 |
|
| 1981 |
Ireland RE, Daub JP. Synthesis of chiral subunits for macrolide synthesis: The Prelog-Djerassi lactone and derivatives Journal of Organic Chemistry. 46: 479-485. DOI: 10.1021/Jo00316A001 |
0.539 |
|
| 1981 |
Ireland RE, Wuts PGM, Ernst B. 3-Acyltetramic acid antibiotics. 1. Synthesis of tirandamycic acid Journal of the American Chemical Society. 103: 3205-3207. DOI: 10.1021/Ja00401A047 |
0.584 |
|
| 1981 |
Ireland RE, Godfrey JD, Thaisrivongs S. Efficient, stereoselective total synthesis of (.+-.)-aphidicolin Journal of the American Chemical Society. 103: 2446-2448. DOI: 10.1021/Ja00399A068 |
0.528 |
|
| 1981 |
IRELAND RE, GODFREY JD, THAISRIVONGS S. ChemInform Abstract: EFFICIENT, STEREOSELECTIVE TOTAL SYNTHESIS OF (.+-.)-APHIDICOLIN Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198133315 |
0.457 |
|
| 1981 |
IRELAND RE, HAEBICH D. ChemInform Abstract: PHEROMONE SYNTHESES - MODEL REACTIONS FOR THE SYNTHESIS OF POLYETHER ANTIBIOTICS Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198131328 |
0.332 |
|
| 1981 |
IRELAND RE, VEVERT J. ChemInform Abstract: TOTAL SYNTHESIS OF (+) AND (-) NONACTIC ACIDS FROM CARBOHYDRATES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198126338 |
0.376 |
|
| 1981 |
IRELAND RE, DAUB JP. ChemInform Abstract: THE SYNTHESIS OF CHIRAL SUBUNITS FOR MACROLIDE SYNTHESIS: THE PRELOG-DJERASSI LACTONE AND DERIVATIVES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198126248 |
0.459 |
|
| 1981 |
Ireland RE, Häbich D. Pheromonsynthesen ‐ Modellreaktionen zur Synthese von Polyether‐Antibiotika Chemische Berichte. 114: 1418-1427. DOI: 10.1002/Cber.19811140419 |
0.32 |
|
| 1981 |
Ireland RE, Habich D. Pherome syntheses - Model reactions for the synthesis of polyether antibiotics | PHEROMONSYNTHESEN - MODELLREAKTIONEN ZUR SYNTHESE VON POLYETHER-ANTIBIOTIKA Chemische Berichte. 114: 1418-1427. |
0.337 |
|
| 1980 |
Ireland RE, Vevert JP. A chiral total synthesis of (-)- and ( + )-nonactic acids from carbohydrate precursors and the definition of the transition for the enolate claisen rearrangement in heterocyclic systems Journal of Organic Chemistry. 45: 4259-4260. DOI: 10.1021/Jo01309A050 |
0.442 |
|
| 1980 |
Ireland RE, Brown FR. Macrocyclic lactone formation through sulfide contraction. Synthesis of (±)-diplodialide A Journal of Organic Chemistry. 45: 1868-1880. DOI: 10.1021/Jo01298A022 |
0.388 |
|
| 1980 |
Ireland RE, Wilcox CS. New and efficient synthesis of 6-deoxy-L-gulose Journal of Organic Chemistry. 45: 197-203. DOI: 10.1021/Jo01290A001 |
0.642 |
|
| 1980 |
Ireland RE, Thaisrivongs S, Vanier N, Wilcox CS. Enolate Claisen rearrangement of esters from furanoid and pyranoid glycals Journal of Organic Chemistry. 45: 48-61. DOI: 10.1021/Jo01289A012 |
0.67 |
|
| 1980 |
Ireland RE, McGarvey GJ, Anderson RC, Badoud R, Fitzsimmons B, Thaisrivongs S. A chiral synthesis of the left-side aldehyde for lasalocid A synthesis [23] Journal of the American Chemical Society. 102: 6178-6180. DOI: 10.1021/Ja00539A051 |
0.518 |
|
| 1980 |
Ireland RE, Thaisrivongs S, Wilcox CS. Total synthesis of lasalocid A (X537A) Journal of the American Chemical Society. 102: 1155-1157. DOI: 10.1021/Ja00523A038 |
0.744 |
|
| 1980 |
Ireland RE, Häbich D. A convergent scheme for the synthesis of spiroketals and the synthesis of (±)-chalcogran Tetrahedron Letters. 21: 1389-1392. DOI: 10.1016/S0040-4039(00)92727-8 |
0.497 |
|
| 1980 |
IRELAND RE, MCGARVEY GJ, ANDERSON RC, BADOUD R, FITZSIMMONS B, THAISRIVONGS S. ChemInform Abstract: A CHIRAL SYNTHESIS OF THE LEFT-SIDE ALDEHYDE FOR LASALOCID A SYNTHESIS Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198050335 |
0.437 |
|
| 1980 |
IRELAND RE, BROWN FRJ. ChemInform Abstract: MACROCYCLIC LACTONE FORMATION THROUGH SULFIDE CONTRACTION. SYNTHESIS OF (.+-.)-DIPLODIALIDE A Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198044265 |
0.436 |
|
| 1980 |
IRELAND RE, HAEBICH D. ChemInform Abstract: A CONVERGENT SCHEME FOR THE SYNTHESIS OF SPIROKETALS AND THE SYNTHESIS OF (+)-CHALCOGRAN Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198032337 |
0.375 |
|
| 1980 |
IRELAND RE, THAISRIVONGS S, VANIER N, WILCOX CS. ChemInform Abstract: ENOLATE CLAISEN REARRANGEMENT OF ESTERS FROM FURANOID AND PYRANOID GLYCALS Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198023119 |
0.635 |
|
| 1980 |
IRELAND RE, THAISRIVONGS S, WILCOX CS. ChemInform Abstract: TOTAL SYNTHESIS OF LASALOCID A (X537A) Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198019316 |
0.722 |
|
| 1980 |
Ireland RE, Thaisrivongs S, Wilcox CS. Total synthesis of lasalocid A (X537A) [3] Journal of the American Chemical Society. 102: 1155-1157. |
0.488 |
|
| 1979 |
Ireland RE, Wilcox CS, Thaisrivongs S, Vanier NR. The generation of C-glycosides through the enolate Claisen rearrangement Canadian Journal of Chemistry. 57: 1743-1745. DOI: 10.1139/V79-278 |
0.683 |
|
| 1979 |
Ireland RE, Aristoff PA. Experiments directed toward the total synthesis of terpenes. 24. On the π route to aphidicolin: Synthesis of 18,19-bisnoraphidicolan-3-one Journal of Organic Chemistry. 44: 4323-4331. DOI: 10.1021/Jo01338A018 |
0.546 |
|
| 1979 |
Ireland RE, Aristoff PA, Hoyng CF. Experiments directed toward the total synthesis of terpenes. 23. Synthesis of 4a-methyl-4,4a,7,8-tetrahydro-9H-benzocycloheptene-2(3H),5(6H)-dione (B-homo Wieland-Miescher ketone): A versatile intermediate for terpene synthesis Journal of Organic Chemistry. 44: 4318-4322. DOI: 10.1021/Jo01338A017 |
0.385 |
|
| 1979 |
Ireland RE, Thompson WJ. An approach to the total sythesis of chlorothricolide: The synthesis of the top half Journal of Organic Chemistry. 44: 3041-3052. DOI: 10.1021/Jo01331A017 |
0.463 |
|
| 1979 |
Ireland RE, Thompson WJ. The facile reduction of methoxyethoxymethyl esters with lithium triethylborohydride Tetrahedron Letters. 20: 4705-4708. DOI: 10.1016/S0040-4039(01)86689-2 |
0.375 |
|
| 1979 |
IRELAND RE, THOMPSON WJ. ChemInform Abstract: AN APPROACH TO THE TOTAL SYNTHESIS OF CHLOROTHRICOLIDE: THE SYNTHESIS OF THE TOP HALF Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197951121 |
0.461 |
|
| 1978 |
Ireland RE, Wilcox CS, Thaisrivongs S. An efficient method for the preparation of furanoid and pyranoid glycals Journal of Organic Chemistry. 43: 786-787. DOI: 10.1021/Jo00398A078 |
0.6 |
|
| 1978 |
IRELAND RE, WILCOX CS, THAISRIVONGS S. ChemInform Abstract: AN EFFICIENT METHOD FOR THE PREPARATION OF FURANOID AND PYRANOID GLYCALS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197827216 |
0.584 |
|
| 1977 |
Ireland RE, Giger R, Kamata S. Studies on the total synthesis of steroidal antibiotics. 3. Generation and correlation of Tetracyclic derivatives from the degradation of fusidic acid and total synthesis. The Journal of Organic Chemistry. 42: 1276-82. PMID 845710 DOI: 10.1002/Chin.197733185 |
0.508 |
|
| 1977 |
Ireland RE, Beslin P, Giger R, Hengartner U, Kirst HA, Maag H. Studies on the total synthesis of steroidal antibiotics. 2. Two convergent schemes for the synthesis of tetracyclic intermediates. The Journal of Organic Chemistry. 42: 1267-76. PMID 845709 DOI: 10.1002/Chin.197733184 |
0.48 |
|
| 1977 |
IRELAND RE, GIGER R, KAMATA S. ChemInform Abstract: STUDIES ON THE TOTAL SYNTHESIS OF STEROIDAL ANTIBIOTICS. 3. GENERATION AND CORRELATION OF TETRACYCLIC DERIVATIVES FROM THE DEGRADATION OF FUSIDIC ACID AND TOTAL SYNTHESIS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197733185 |
0.427 |
|
| 1977 |
IRELAND RE, BESLIN P, GIGER R, HENGARTNER U, KIRST HA, MAAG H. ChemInform Abstract: STUDIES ON THE TOTAL SYNTHESIS OF STEROIDAL ANTIBIOTICS. 2. TWO CONVERGENT SCHEMES FOR THE SYNTHESIS OF TETRACYCLIC INTERMEDIATES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197733184 |
0.394 |
|
| 1976 |
Ireland RE, Mueller RH, Willard AK. The ester enolate claisen rearrangement. Construction of the prostanoid skeleton Journal of Organic Chemistry. 41: 986-996. DOI: 10.1021/Jo00868A018 |
0.383 |
|
| 1976 |
Ireland RE, Mueller RH, Willard AK. The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation Journal of the American Chemical Society. 98: 2868-2877. DOI: 10.1021/Ja00426A033 |
0.381 |
|
| 1976 |
Ireland RE, Walba1 DM. The total synthesis of (±)-friedelin, an unsymmetrical, pentacyclic triterpene Tetrahedron Letters. 17: 1071-1074. DOI: 10.1016/S0040-4039(00)93753-5 |
0.378 |
|
| 1976 |
Ireland RE, Mueller RH, Willard AK. Ester enolate Claisen rearrangement. Construction of the prostanoid skeleton Cheminform. 7. DOI: 10.1002/Chin.197626350 |
0.383 |
|
| 1976 |
IRELAND RE, WALBA DM. ChemInform Abstract: THE TOTAL SYNTHESIS OF (.+-.)-FRIEDELIN, AN UNSYMMETRICAL PENTACYCLIC TRITERPENE Chemischer Informationsdienst. 7. DOI: 10.1002/chin.197625330 |
0.686 |
|
| 1975 |
Ireland RE, McKenzie TC, Trust RI. Total synthesis of terpenes. XXII. Polyene cyclization approach to tetradecahydropicene derivatives for pentacyclic triterpene synthesis The Journal of Organic Chemistry. 40: 1007-1017. DOI: 10.1021/Jo00896A004 |
0.55 |
|
| 1975 |
Ireland RE, Bey P, Cheng KF, Czarny RJ, Moser JF, Trust RI. Experiments directed toward the total synthesis of terpenes. XXI. An alternate total synthesis of dl-alnusenone via polyene cyclization Journal of Organic Chemistry. 40: 1000-1007. DOI: 10.1021/Jo00896A003 |
0.564 |
|
| 1975 |
Ireland RE, Kowalski CJ, Tilley JW, Walba DM. Total synthesis of terpenes. XX. Total synthesis of (+-)-shionone, a tetracyclic triterpene The Journal of Organic Chemistry. 40: 990-1000. DOI: 10.1021/Jo00896A002 |
0.715 |
|
| 1975 |
Ireland RE, Dawson MI, Kowalski CJ, Lipinski CA, Marshall DR, Tilley JW, Bordner J, Trus BL. Total synthesis of terpenes. XIX. Synthesis of 8-methoxy-4a.beta., 10b.beta., 12a.alpha.-trimethyl-3,4,4a,4b.alpha.,5,6,10b,11,12,12a-decahydrochrysen-1(2H)-one, a key intermediate in the total synthesis of (+-)-shionone The Journal of Organic Chemistry. 40: 973-990. DOI: 10.1021/Jo00896A001 |
0.318 |
|
| 1975 |
Ireland RE, Willard AK. The stereoselective generation of ester enolates Tetrahedron Letters. 16: 3975-3978. DOI: 10.1016/S0040-4039(00)91213-9 |
0.382 |
|
| 1975 |
IRELAND RE, MCKENZIE TC, TRUST RI. ChemInform Abstract: EXPERIMENTS DIRECTED TOWARD THE TOTAL SYNTHESIS OF TERPENES PART 22, A POLYENE CYCLIZATION APPROACH TO TETRADECAHYDROPICENE DERIVATIVES FOR PENTACYCLIC TRITERPENE SYNTHESIS Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197532383 |
0.551 |
|
| 1975 |
IRELAND RE, DAWSON MI, KOWALSKI CJ, LIPINSKI CA, MARSHALL DR, TILLEY JW, BORDNER J, TRUS BL. ChemInform Abstract: EXPERIMENTS DIRECTED TOWARD THE TOTAL SYNTHESIS OF TERPENES PART 19, SYNTHESIS OF 8-METHOXY-4A BETA,10B BETA,12A ALPHA-TRIMETHYL-3,4,4A,4B ALPHA,5,6,10B,11,12A-DECAHYDROCHRYSEN-1(2H)-ONE, A KEY INTERMEDIATE IN THE TOTAL SYNTHESIS OF ( Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197532381 |
0.329 |
|
| 1975 |
IRELAND RE, KOWALSKI CJ, TILLEY JW, WALBA DM. ChemInform Abstract: EXPERIMENTS DIRECTED TOWARD THE TOTAL SYNTHESIS OF TERPENES PART 20, TOTAL SYNTHESIS OF (+-)-SHIONONE, A TETRACYCLIC TRITERPENE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197532380 |
0.707 |
|
| 1975 |
IRELAND RE, BEY P, CHENG KF, CZARNY RJ, MOSER JF, TRUST RI. ChemInform Abstract: EXPERIMENTS DIRECTED TOWARD THE TOTAL SYNTHESIS OF TERPENES PART 21, AN ALTERNATE TOTAL SYNTHESIS OF DL-ALNUSENONE VIA POLYENE CYCLIZATION Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197532379 |
0.489 |
|
| 1975 |
Ireland RE, Dawson MI, Kowalski CJ, Lipinski CA, Marshall DR, Tilley JW, Bordner J, Trus BL. Experiments directed toward the total synthesis of terpenes. XIX. Synthesis of 8-methoxy-4aβ,10bβ,12aα-trimethyl-3,4,4a,4bα,5,6,10b,11, 12,12a-decahydrochrysen-1(2H)-one, a key intermediate in the total synthesis of (±)-shionone Journal of Organic Chemistry. 40: 973-993. |
0.306 |
|
| 1975 |
Ireland RE, McKenzie TC, Trust RI. Experiments directed toward the total synthesis of terpenes. XXII. A polyene cyclization approach to tetradecahydropicene derivatives for pentacyclic triterpene synthesis Journal of Organic Chemistry. 40: 1007-1017. |
0.453 |
|
| 1974 |
Ireland RE, Lipinski CA, Kowalski CJ, Tilley JW, Walba DM. Total synthesis of dl-shionone, a tetracyclic triterpene [16] Journal of the American Chemical Society. 96: 3333-3335. DOI: 10.1021/Ja00817A061 |
0.712 |
|
| 1974 |
IRELAND RE, LIPINSKI CA, KOWALSKI CJ, TILLEY JW, WALBA DM. ChemInform Abstract: TOTAL SYNTHESIS OF DL-SHIONONE, A TETRACYCLIC TRITERPENE Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197429408 |
0.684 |
|
| 1974 |
IRELAND RE, DAWSON MI, WELCH SC, HAGENBACH A, BORDNER J, TRUS B. ChemInform Abstract: EXPERIMENTS DIRECTED TOWARD THE TOTAL SYNTHESIS OF TERPENES PART 18, THE CONVERGENT, STEREOSELECTIVE TOTAL SYNTHESIS OF THE UNSYMMETRICAL PENTACYCLIC TRITERPENE ALNUSENONE Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197404354 |
0.565 |
|
| 1973 |
Ireland RE, Dawson MI, Welch SC, Hagenbach A, Bordner J, Trus B. Total synthesis of terpenes, XVIII. Convergent, stereoselective total synthesis of the unsymmetrical pentacyclic triterpene alnusenone Journal of the American Chemical Society. 95: 7829-7841. DOI: 10.1021/Ja00804A045 |
0.577 |
|
| 1973 |
Ireland RE, Dawson MI, Welch SC, Hagenbach A, Bordner J, Trus B. Experiments directed toward the total synthesis of terpenes. XVIII. The convergent, stereoselective total synthesis of the unsymmetrical pentacyclic triterpene alnusenone Journal of the American Chemical Society. 95: 7829-7841. |
0.474 |
|
| 1972 |
Ireland RE, Hengartner U. Studies on the total synthesis of steroidal antibiotics. I. An efficient, stereoselective method for the formation of trans-syn-trans-perhydrophenanthrene derivatives. Journal of the American Chemical Society. 94: 3652-3. PMID 5032972 DOI: 10.1021/Ja00765A079 |
0.49 |
|
| 1972 |
Ireland RE, Pfister G, Dawson JD, Dennis D, Stanford RH. The Synthesis12 And Single Crystal X-rayStructure Determination1b Of 9α-Cyand- 19-Nortestosterone Synthetic Communications. 2: 175-180. DOI: 10.1080/00397917208081761 |
0.427 |
|
| 1972 |
Ireland RE, Mueller RH. Claisen rearrangement of allyl esters Journal of the American Chemical Society. 94: 5897-5898. DOI: 10.1021/Ja00771A062 |
0.441 |
|
| 1972 |
Ireland RE, Baldwin SW, Welch SC. Experiments directed toward the total synthesis of terpenes. XVII. Development of methods for the synthesis of pentacyclic triterpenes based on a mechanistic interpretation of the stereochemical outcome of the Friedel-Crafts cyclialkylation reaction Journal of the American Chemical Society. 94: 2056-2066. DOI: 10.1021/Ja00761A044 |
0.686 |
|
| 1972 |
Ireland RE, Baldwin SW, Welch SC. Untersuchungen Im Hinblick Auf Die Totalsynth. Von Terpenen 17. Mitt. Entwicklung Von Methoden Zur Synth. Pentacyclischer Triterpene Auf Der Grundlage Einer Mechanistischen Interpretation Der Stereochemischen Faktoren Der Friedel-Craf Cheminform. 3. DOI: 10.1002/Chin.197224288 |
0.576 |
|
| 1972 |
Ireland RE, Mueller RH. The Claisen rearrangement of allyl esters [5] Journal of the American Chemical Society. 94: 5897-5898. |
0.332 |
|
| 1970 |
Ireland RE, Welch SC. Total synthesis of DL-alnusenone Journal of the American Chemical Society. 92: 7232-7234. DOI: 10.1021/Ja00727A053 |
0.565 |
|
| 1970 |
Ireland RE, et al. .. Total synthesis of an unsymmetrical pentacyclic triterpene. DL-germanicol Journal of the American Chemical Society. 92: 5743-5746. DOI: 10.1021/Ja00722A041 |
0.572 |
|
| 1970 |
Ireland RE, Marshall DR, Tilley JW. Convenient, stereoselective synthesis of 9,10-dimethyl-trans-1-decalones through the protolysis of fused methoxycyclopropanes Journal of the American Chemical Society. 92: 4754-4756. DOI: 10.1021/Ja00718A058 |
0.562 |
|
| 1970 |
Ireland RE, Dawson MI, Bordner J, Dickerson RE. Stereospecific synthesis and acid-catalyzed cyclization of 4,6-dimethyl-trans-5,9-decadienal Journal of the American Chemical Society. 92: 2568-2570. DOI: 10.1021/Ja00711A070 |
0.498 |
|
| 1970 |
Ireland RE, Dawson MI, Lipinski CA. The utility of the coupling reaction between propargyl grignard reagent and allylic halides for the synthesis of acetylenes Tetrahedron Letters. 11: 2247-2250. DOI: 10.1016/S0040-4039(01)98200-0 |
0.422 |
|
| 1970 |
Ireland RE, Baldwin SW, Dawson DJ, Dawson MI, Dolfini JE, Newbould J, Johnson WS, Brown M, Crawford RJ, Hudrlik PF, Rasmussen GH, Schmiegel KK. Totalsynth. Eines Unsymmetrischen, Pentacyclischen Triterpens, Dl-Germanicol Cheminform. 1. DOI: 10.1002/Chin.197049405 |
0.697 |
|
| 1970 |
Ireland RE, Marshall DR, Tilley JW. Bequeme, Stereoselektive Synth. Von 9,10-Dimethyl-Trans-Decalonen-(1) Durch Protolyse Von Ankondensierten Methoxy-Cyclopropanen Cheminform. 1. DOI: 10.1002/Chin.197043330 |
0.301 |
|
| 1970 |
IRELAND RE, EVANS DA, LOELIGER P, BORDNER J, STANFORD RH, DICKERSON RE. ChemInform Abstract: VERSUCHE ZU EINER TOTALSYNTH. VON TERPENEN 16. MITT. STRUKTUR UND STEREOCHEMIE VON ZWEI DECAHYDROPICEN-DERIVATEN Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197013234 |
0.424 |
|
| 1970 |
IRELAND RE, EVANS DA, GLOVER D, RUBOTTOM GM, YOUNG H. ChemInform Abstract: VERSUCHE ZU EINER TOTALSYNTH. VON TERPENEN 15. MITT. SYNTH. VON 3,10-DIMETHOXY-6A BETA,12B BETA-DIMETHYL-5,6,6A,6B ALPHA,7,8,12B,13-OCTAHYDROPICEN, EINER POTENTIELLEN ZWISCHENSTUFE BEI TRITERPENSYNTH. Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197013233 |
0.375 |
|
| 1970 |
Ireland RE, Welch SC. The total synthesis of DL-alnusenone [22] Journal of the American Chemical Society. 92: 7232-7234. |
0.481 |
|
| 1970 |
Ireland RE, Baldwin SW, Dawson DJ, Dawson MI, Dolfini JE, Newbould J, Johnson WS, Brown M, Crawford RJ, Hudrlik PF, Rasmussen GH, Schmiegel KK. The total synthesis of an unsymmetrical pentacyclic triterpene. DL-germanicol [13] Journal of the American Chemical Society. 92: 5743-5746. |
0.75 |
|
| 1970 |
Ireland RE, Dawson MI, Bordner J, Dickerson RE. The stereospecific synthesis and acid-catalyzed cyclization of 4,6-dimethyl-trans-5,9-decadienal [18] Journal of the American Chemical Society. 92: 2568-2570. |
0.401 |
|
| 1970 |
Ireland RE, Marshall DR, Tilley JW. A convenient, stereoselective synthesis of 9,10-dimethyl-trans-1-decalones through the protolysis of fused methoxycyclopropanes [20] Journal of the American Chemical Society. 92: 4754-4756. |
0.477 |
|
| 1969 |
Ireland RE, Evans DA, Loeliger P, Bordner J, Stanford RH, Dickerson RE. Total synthesis of terpenes. XVI. Structure and stereochemistry of two decahydropicene derivatives The Journal of Organic Chemistry. 34: 3729-3739. DOI: 10.1021/Jo01264A002 |
0.569 |
|
| 1969 |
Ireland RE, Evans DA, Glover D, Rubottom GM, Young H. Total synthesis of terpenes. XV. Synthesis of 3,10-dimethoxy-6a.beta.,12b.beta.-dimethyl-5,6,6a,6b.alpha.,7,8,12b,13-octahydropicene, a potential intermediate in triterpene synthesis The Journal of Organic Chemistry. 34: 3717-3729. DOI: 10.1021/Jo01264A001 |
0.474 |
|
| 1969 |
Ireland RE, Mander LN. Experiments directed toward the total synthesis of terpenes. XIII. The construction of the lactone ring of rosenonolactone Journal of Organic Chemistry. 34: 142-152. DOI: 10.1021/Jo00838A032 |
0.631 |
|
| 1969 |
Ireland RE, Pfister G. A new method for the synthesis of structurally specific olefins from enolate anions Tetrahedron Letters. 10: 2145-2148. DOI: 10.1016/S0040-4039(01)88107-7 |
0.413 |
|
| 1969 |
Ireland RE, Evans DA, Löliger P, Bordner J, Stanford RH, Dickerson RE. Experiments directed toward the total synthesis of terpenes. XVI. The structure and stereochemistry of two decahydropicene derivatives Journal of Organic Chemistry. 34: 3729-3739. |
0.356 |
|
| 1969 |
Ireland RE, Evans DA, Glover D, Rubottom GM, Young H. Experiments directed toward the total synthesis of terpenes. XV. The synthesis of 3,10-dimethoxy-6aβ,12bβ-dimethyl-5,6,6a,6bα,7,8,12b,13- octahydropicene, a potential intermediate in triterpene synthesis Journal of Organic Chemistry. 34: 3717-3729. |
0.386 |
|
| 1968 |
Giarrusso F, Ireland RE. Experiments directed toward the total synthesis of terpenes. XII. A stereoselective synthesis of (±)-desoxypodocarpic acid and (±)-13-methoxydesoxypodocarpic acid Journal of Organic Chemistry. 33: 3560-3565. DOI: 10.1021/Jo01273A045 |
0.395 |
|
| 1967 |
Ireland RE, Mander LN. Experiments directed toward the total synthesis of terpenes. XI. The total synthesis of (±)-rimuene and (±)-13-epi-rimuene Journal of Organic Chemistry. 32: 689-696. DOI: 10.1021/Jo01278A041 |
0.582 |
|
| 1966 |
Ireland RE, Kierstead RC. Experiments directed toward the total synthesis of terpenes. X. A stereoselective scheme for diterpenoid resin acid synthesis. The Journal of Organic Chemistry. 31: 2543-59. PMID 5917444 DOI: 10.1021/Jo01346A026 |
0.456 |
|
| 1966 |
Bell RA, Ireland RE, Mander LN. Experiments directed toward the total synthesis of terpenes. IX. The total synthesis of (+or-)-hibaene and the oxygenation of some tetracyclic diterpenes. The Journal of Organic Chemistry. 31: 2536-42. PMID 5917443 DOI: 10.1021/Jo01346A025 |
0.653 |
|
| 1966 |
Bell RA, Ireland RE, Partyka RA. Experiments directed toward the total synthesis of terpenes. 8. The total synthesis of (+or-)-kaurene and,(+or-)-atisirene. The Journal of Organic Chemistry. 31: 2530-6. PMID 5917442 DOI: 10.1021/Jo01346A024 |
0.55 |
|
| 1966 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. VII. The synthesis of (+or-)-8-beta-carbomethoxy-13-oxopodocarpanone, a degradation product of phyllocladene. The Journal of Organic Chemistry. 31: 2526-30. PMID 5917441 DOI: 10.1021/Jo01346A023 |
0.644 |
|
| 1966 |
Bell RA, Ireland RE, Mander LN. Experiments directed toward the total synthesis of terpenes. IX. The total synthesis of (±)-hibaene and the oxygenation of some tetracyclic diterpenes Journal of Organic Chemistry. 31: 2536-2542. |
0.579 |
|
| 1965 |
Ireland RE, Mander LN. The total synthesis of (±)-hibaene Tetrahedron Letters. 6: 2627-2632. DOI: 10.1016/S0040-4039(00)90219-3 |
0.525 |
|
| 1964 |
Ireland RE, Mander LN. The total synthesis of dl-rimuene Tetrahedron Letters. 5: 3453-3457. DOI: 10.1016/S0040-4039(01)89410-7 |
0.669 |
|
| 1963 |
Chaykovsky M, Ireland RE. An approach to the total synthesis of steroids Journal of Organic Chemistry. 28: 748-755. DOI: 10.1021/Jo01038A038 |
0.465 |
|
| 1963 |
Ireland RE, Newbould J. Experiments directed toward the total synthesis of terpenes. VI. The stereochemistry of isopimaric acid Journal of Organic Chemistry. 28: 23-26. DOI: 10.1021/Jo01036A004 |
0.456 |
|
| 1963 |
Church RF, Ireland RE. Experiments directed toward the total synthesis of terpenes. V. The synthesis of the (±)-9-isopimaradienes Journal of Organic Chemistry. 28: 17-23. DOI: 10.1021/Jo01036A003 |
0.443 |
|
| 1963 |
Ireland RE, Schiess PW. Experiments directed toward the total synthesis of terpenes. IV. The synthesis of (±)-sandaracopimaradiene and (±)-pimaradiene Journal of Organic Chemistry. 28: 6-16. DOI: 10.1021/Jo01036A002 |
0.376 |
|
| 1962 |
Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. III. The use of trans-Δ6-octalone-1 in the preparation of dicyclic intermediates Journal of Organic Chemistry. 27: 1620-1627. DOI: 10.1021/Jo01052A032 |
0.669 |
|
| 1962 |
Ireland RE, Marshall JA. The n-butylthiomethylene blocking group Journal of Organic Chemistry. 27: 1615-1619. DOI: 10.1021/Jo01052A031 |
0.509 |
|
| 1962 |
Church RF, Ireland RE, Marshall JA. Experiments directed toward the total synthesis of terpenes. II. The synthesis of dl-6-keto-5,5,9-trimethyl-2-methylene-trans-decalyl-1α-acetic acid and derivatives Journal of Organic Chemistry. 27: 1118-1125. DOI: 10.1021/Jo01051A002 |
0.686 |
|
| 1962 |
Church RF, Ireland RE, Shridhar DR. Experiments directed toward the total synthesis of terpenes. I. The synthesis of 1β,9-dimethyl-6,6-ethylenedioxy-cis-decalone-2 Journal of Organic Chemistry. 27: 707-714. DOI: 10.1021/Jo01050A001 |
0.468 |
|
| 1962 |
Bell RA, Ireland RE, Partyka RA. The total synthesis of dl-kaurene [1] Journal of Organic Chemistry. 27: 3741-3742. |
0.481 |
|
| 1962 |
Ireland RE, Kierstead RC. A stereoselective total synthesis of dl-dehydroabietic acid [4] Journal of Organic Chemistry. 27: 703-704. |
0.39 |
|
| 1961 |
Church RF, Ireland RE, Marshall JA. A novel approach to a key intermediate in the total synthesis of α-onocerin Tetrahedron Letters. 2: 34-38. DOI: 10.1016/S0040-4039(01)99201-9 |
0.614 |
|
| 1961 |
Church RF, Ireland RE. The synthesis of the dl-9-iso-pimaradienes and the revision of the structures of isopimaric acid and rimuene Tetrahedron Letters. 2: 493-498. DOI: 10.1016/S0040-4039(00)71760-6 |
0.303 |
|
| 1960 |
Church RF, Ireland RE, Marshall JA. The stereospecific total synthesis of d1-8β-carbomethoxy-13-oxopodocarpane, a degradation product of phyllocladene Tetrahedron Letters. 1: 1-4. DOI: 10.1016/S0040-4039(01)99337-2 |
0.557 |
|
| 1960 |
Ireland RE, Schiess PW. The synthesis of dl-sandaracopimaradiene, dl-pimaradiene and some observations on the structure of rimuene Tetrahedron Letters. 1: 37-43. |
0.313 |
|
| 1959 |
Ireland RE, Marshall JA. The n-butylthiomethylene grouping: A superior blocking group for the alkylation of ketones [12] Journal of the American Chemical Society. 81: 6336-6337. DOI: 10.1021/Ja01532A064 |
0.539 |
|
| 1959 |
Ireland RE, Marshall JA. A new synthetic method for the preparation of α-substituted β-ketoesters [4] Journal of the American Chemical Society. 81: 2907-2908. DOI: 10.1021/Ja01520A073 |
0.577 |
|
| 1957 |
Johnson WS, Christiansen RG, Ireland RE. A total synthesis of estrone and 14-isoestrone Journal of the American Chemical Society. 79: 1995-2005. DOI: 10.1021/Ja01565A065 |
0.735 |
|
| Show low-probability matches. |
