| Year |
Citation |
Score |
| 2018 |
Tompkins DC, Nelson RB, Dolby LJ, Gribble GW. Synthesis of 7‐Oxo‐1,2,3,4,6,7,12,12b‐octahydroindolo[2,3‐a]quinolizine Journal of Heterocyclic Chemistry. 55: 2168-2171. DOI: 10.1002/Jhet.3251 |
0.521 |
|
| 2018 |
Tompkins DC, Nelson RB, Dolby LJ, Gribble GW. Synthesis of 7-Oxo-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a
]quinolizine Journal of Heterocyclic Chemistry. 55: 2168-2171. DOI: 10.1002/Jhet.3130 |
0.49 |
|
| 2006 |
Garst ME, Dolby LJ, Esfandiari S, Okrent RA, Avey AA. Studies of the condensation of sulfones with ketones and aldehydes. The Journal of Organic Chemistry. 71: 553-6. PMID 16408963 DOI: 10.1021/Jo051947S |
0.364 |
|
| 2006 |
Garst ME, Dolby LJ, Esfandiari S, Okrent RA, Avey AA. Studies of the condensation of sulfones with ketones and aldehydes Journal of Organic Chemistry. 71: 553-556. DOI: 10.1021/jo051947s |
0.304 |
|
| 1981 |
Koyama Y, Yokose K, Dolby LJ. Isolation, characterization and synthesis of pimprinine, pimprinethine and pimprinaphine, metabolites of streptoverticillium olivoreticuli Agricultural and Biological Chemistry. 45: 1285-1287. DOI: 10.1271/Bbb1961.45.1285 |
0.303 |
|
| 1979 |
Cooper GK, Dolby LJ. Convenient synthesis of the 2-methyl-4-hydroxybut-2-enolide moiety of strigol Journal of Organic Chemistry. 44: 3414-3416. DOI: 10.1021/Jo01333A034 |
0.346 |
|
| 1977 |
Sakai S, Yamanaka E, Dolby LJ. Transformation of indole alkaloids. III. The partial synthesis of protopine type indole alkaloid 'burnamicine' (Japanese) Yakugaku Zasshi. 97: 309-319. PMID 559080 DOI: 10.1248/Yakushi1947.97.3_309 |
0.319 |
|
| 1977 |
McCrae DA, Dolby L. Total synthesis of (.+-.)-acorone The Journal of Organic Chemistry. 42: 1607-1610. DOI: 10.1021/Jo00429A028 |
0.358 |
|
| 1976 |
Dolby LJ, Hanson G. A convenient synthesis of a hydrindan precursor to strigol Journal of Organic Chemistry. 41: 563-564. DOI: 10.1021/Jo00865A036 |
0.382 |
|
| 1974 |
Dolby LJ, Skold CN. Model studies of the synthesis of the a ring of gibberellic acid Journal of the American Chemical Society. 96: 3276-3279. DOI: 10.1021/Ja00971A062 |
0.36 |
|
| 1971 |
Dolby LJ, Esfandiari S, Elliger CA, Marshall KS. Synthesis of the B, C, and D rings of gibberellic acid The Journal of Organic Chemistry. 36: 1277-1285. DOI: 10.1021/Jo00808A024 |
0.332 |
|
| 1970 |
Dolby LJ, Biere H. Total synthesis of (+-)-dasycarpidone, (+-)-epidasycarpidone, and (+-)-epiuleine The Journal of Organic Chemistry. 35: 3843-3845. DOI: 10.1021/Jo00836A058 |
0.358 |
|
| 1969 |
Dolby LJ, Wilkins CL. Structure and reactivity of highly substituted cyclobutyl tosylates Tetrahedron. 25: 2381-2391. DOI: 10.1016/S0040-4020(01)82786-1 |
0.638 |
|
| 1968 |
Dolby LJ, Wilkins CL, Rodia RM. The mechanism of the Prins reaction. VII. Kinetic studies of the Prins reaction of styrenes Journal of Organic Chemistry. 33: 4155-4158. DOI: 10.1021/Jo01275A031 |
0.626 |
|
| 1968 |
Dolby LJ, Gribble GW. New reactions of 3-vinylindoles Tetrahedron. 24: 6377-6386. DOI: 10.1016/S0040-4020(01)96829-2 |
0.334 |
|
| 1968 |
Dolby L, Gribble G. New reactions of 3-vinylindoles Tetrahedron. 24: 6377-6386. DOI: 10.1016/S0040-4020(01)96829-2 |
0.432 |
|
| 1967 |
Dolby LJ, Sakai S. The C--D ring cleavage of dihydrocorynantheine derivatives. The partial synthesis of dihydroburnamicine. Tetrahedron. 23: 1-9. PMID 6037282 DOI: 10.1016/S0040-4020(01)83280-4 |
0.338 |
|
| 1967 |
Dolby L, Gribble G. The Conversion of Tetrahydro-β-carbolines into 2-Acylindoles The Journal of Organic Chemistry. 32: 1391-1398. DOI: 10.1021/Jo01280A600 |
0.415 |
|
| 1966 |
Dolby LJ, Wilkins C, Frey TG. The mechanism of the Prins reaction. V. The Prins reaction of styrenes Journal of Organic Chemistry. 31: 1110-1116. DOI: 10.1021/Jo01342A029 |
0.622 |
|
| 1966 |
Dolby LJ, Milligan RJ. A Model Study of the Synthesis of the A Ring of Gibberellic Acid1 Journal of the American Chemical Society. 88: 3276-3279. DOI: 10.1021/Ja00817A041 |
0.36 |
|
| 1966 |
Dolby LJ, Wilkins C. The solvolysis of and - 3-hydroxy- 2,2,3,4,4-pentamethylcyclobutyl tosylates Tetrahedron Letters. 7: 2751-2757. DOI: 10.1016/S0040-4039(00)62020-8 |
0.661 |
|
| 1966 |
Dolby LJ, Gribble GW. A convenient preparation of indoline Journal of Heterocyclic Chemistry. 3: 124-125. DOI: 10.1002/jhet.5570030202 |
0.431 |
|
| 1966 |
Dolby LJ, Gribble GW. A convenient preparation of indoline Journal of Heterocyclic Chemistry. 3: 124-125. DOI: 10.1002/Jhet.5570030202 |
0.337 |
|
| 1966 |
Dolby LJ, Wilkins C. The solvolysis of cis and trans- 3-hydroxy- 2,2,3,4,4-pentamethylcyclobutyl tosylates Tetrahedron Letters. 7: 2751-2757. |
0.588 |
|
| 1964 |
Dolby LJ, Sakai SI. A new C-D ring cleavage of dihydrocorynantheine derivatives. The partial synthesis of the dihydroburnamicine ring system [29] Journal of the American Chemical Society. 86: 5362-5363. DOI: 10.1021/Ja01077A084 |
0.323 |
|
| 1964 |
Dolby LJ, Wilkins C. The solvolysis of 2,2,4,4-tetramethylcyclobutane derivatives Tetrahedron Letters. 5: 2379-2384. DOI: 10.1016/S0040-4039(01)89453-3 |
0.619 |
|
| 1961 |
Noyce DS, Dolby LJ. Studies of configuration. XI. A new method for the evaluation of conformational free energy differences Journal of Organic Chemistry. 26: 3619-3626. DOI: 10.1021/Jo01068A001 |
0.462 |
|
| 1961 |
Noyce D, Weingarten H, Dolby L. Notes- Rearrangement of Lactones from Substituted 3-Hydroxycyclohexanecarboxylic Acids. The Journal of Organic Chemistry. 26: 2101-2102. DOI: 10.1021/Jo01065A604 |
0.546 |
|
| 1961 |
Noyce DS, Dolby LJ. Studies of configuration. IX. The preparation and stereochemical characterization of some alkyl-3-hyxlroxycyclohexanecarboxylic acids Journal of Organic Chemistry. 26: 1732-1737. DOI: 10.1021/Jo01065A010 |
0.551 |
|
| 1961 |
Noyce DS, Weingarten HI, Dolby LJ. Rearrangement of lactones from substituted 3-hydroxycyclohexanecarboxylic acids Journal of Organic Chemistry. 26: 2101-2102. |
0.548 |
|
| 1960 |
van Tamelen EE, Dolby LJ, Lawton RG. A biogenetically-patterned laboratory synthesis in the strychnine - curare alkaloid series Tetrahedron Letters. 1: 30-35. |
0.652 |
|
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