Year |
Citation |
Score |
2009 |
Isleyen A, Gonsky C, Ronald RC, Garner P. Efficacious preparation of Oppolzer's glycylsultam via the Delépine reaction Synthesis. 1261-1264. DOI: 10.1055/S-0028-1088021 |
0.334 |
|
1998 |
Wahlstrom JL, Ronald RC. Detritylation of Ethers Using Iodine-Alcohol Reagents: An Acid-Catalyzed Reaction. The Journal of Organic Chemistry. 63: 6021-6022. PMID 11672207 DOI: 10.1021/Jo972222U |
0.357 |
|
1987 |
Ruder SM, Ronald RC. Solvolytic hydroperoxide rearrangements V. A stereoselective synthesis of trans-fused butyrolactones Tetrahedron Letters. 28: 135-138. DOI: 10.1016/S0040-4039(00)95668-5 |
0.754 |
|
1987 |
Ronald RC, Ruder SM, S. Lillie T. Solvolytic hydroperoxide rearrangements IV. Selective rearrangement of spiro[5,2]octan-4-ol Tetrahedron Letters. 28: 131-134. DOI: 10.1016/S0040-4039(00)95667-3 |
0.751 |
|
1986 |
Ronald RC, Lillie TS. Solvolytic hydroperoxide rearrangements III. Stereoselective Rearrangements of Methylated Cyclopropyl Carbinols Tetrahedron Letters. 27: 5787-5790. DOI: 10.1016/S0040-4039(00)85327-7 |
0.78 |
|
1985 |
Lillie TS, Ronald RC. Solvolytic hydroperoxide rearrangements. 2. Oxa bicyclic hemiketal peroxides from homoallylic and cyclopropylcarbinyl precursors Journal of Organic Chemistry. 50: 5084-5088. DOI: 10.1021/Jo00225A018 |
0.783 |
|
1985 |
Hillis LR, Ronald RC. Total synthesis of (-)-grahamimycin A1 Journal of Organic Chemistry. 50: 470-473. DOI: 10.1021/Jo00204A009 |
0.759 |
|
1984 |
Ruder SM, Ronald RC. 2-Chloroethyl dimethyl sulfonium iodide. A convenient reagent for spiroannelation of ketones Tetrahedron Letters. 25: 5501-5504. DOI: 10.1016/S0040-4039(01)81610-5 |
0.746 |
|
1984 |
Ronald RC, Wheeler CJ. Synthesis of the simple flavonoid broussonin A Journal of Organic Chemistry. 49: 1658-1660. DOI: 10.1002/Chin.198440140 |
0.446 |
|
1983 |
Ronald RC, Wheeler CJ. Methyl 5-triphenylphosphoranylidenelevulinate: a reagent for homologation of aldehydes to E-.delta.-ene-.gamma.-keto esters The Journal of Organic Chemistry. 48: 138-139. DOI: 10.1021/Jo00149A033 |
0.31 |
|
1983 |
Ronald RC, Lillie TS. Solvolytic hydroperoxide rearrangements. A new ring expansion reaction Journal of the American Chemical Society. 105: 5709-5710. DOI: 10.1021/Ja00355A041 |
0.761 |
|
1983 |
Ronald RC, Winkle MR. Regioselective metallations of (methoxymethoxy)arenes Tetrahedron. 39: 2031-2042. DOI: 10.1016/S0040-4020(01)91921-0 |
0.769 |
|
1983 |
Ronald RC, Wheeler CJ. Methyl 5-(triphenylphosphoranylidene)levulinate: A reagent for homologation of aldehydes to δ-ene γ-keto esters Journal of Organic Chemistry. 48: 138-139. |
0.309 |
|
1982 |
Gewali MB, Ronald RC. Synthesis of allolaurinterol Journal of Organic Chemistry. 47: 2792-2795. DOI: 10.1021/Jo00135A026 |
0.747 |
|
1982 |
Ronald RC, Lansinger JM, Lillie TS, Wheeler CJ. Total synthesis of frustulosin and aurocitrin Journal of Organic Chemistry. 47: 2541-2549. DOI: 10.1021/Jo00134A009 |
0.753 |
|
1982 |
Winkle MR, Ronald RC. Regioselective metalation reactions of some substituted (methoxymethoxy)arenes Journal of Organic Chemistry. 47: 2101-2108. DOI: 10.1021/Jo00132A022 |
0.771 |
|
1982 |
Ronald RC, Lansinger JM, Lillie TS, Wheeler CJ. Total synthesis of frustulosin and aurocitrin Journal of Organic Chemistry. 47: 2541-2549. |
0.756 |
|
1981 |
Hillis LR, Ronald RC. Improved preparation of (+)-(R)-methyloxirane Journal of Organic Chemistry. 46: 3348-3349. |
0.698 |
|
1980 |
Croteau R, Felton M, Ronald RC. Biosynthesis of monoterpenes: preliminary characterization of i-endo-fenchol synthetase from fennel (Foeniculum vulgare) and evidence that no free intermediate is involved in the cyclization of geranyl pyrophosphate to the rearranged product. Archives of Biochemistry and Biophysics. 200: 534-46. PMID 7436421 DOI: 10.1016/0003-9861(80)90385-9 |
0.35 |
|
1980 |
Croteau R, Felton M, Ronald RC. Biosynthesis of monoterpenes: conversion of the acyclic precursors geranyl pyrophosphate and neryl pyrophosphate to the rearranged monoterpenes fenchol and fenchone by a soluble enzyme preparation from fennel (Foeniculum vulgare). Archives of Biochemistry and Biophysics. 200: 524-33. PMID 7436420 DOI: 10.1016/0003-9861(80)90384-7 |
0.374 |
|
1980 |
Winkle MR, Lansinger JM, Ronald RC. 2,5-dimethoxybenzyl alcohol: A convenient self-indicating standard for the determination of organolithium reagents Journal of the Chemical Society, Chemical Communications. 87-88. DOI: 10.1039/C39800000087 |
0.694 |
|
1980 |
Ronald RC, Gewali MB, Ronald BP. Total synthesis of (-)-aplysin and (-)-debromoaplysin Journal of Organic Chemistry. 45: 2224-2229. |
0.741 |
|
1979 |
Lansinger JM, Ronald RC. Reactions of Aromatic Aldehydes with Boron Halides Synthetic Communications. 9: 341-349. DOI: 10.1080/00397917908064161 |
0.773 |
|
1979 |
RONALD RC, LANSINGER JM. ChemInform Abstract: TOTAL SYNTHESIS OF FRUSTULOSIN Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197945175 |
0.782 |
|
1976 |
Ronald RC. A new stereoselective synthesis of (+)-debromoaplysin and (+)-aplysin Tetrahedron Letters. 17: 4413-4416. DOI: 10.1016/0040-4039(76)80130-X |
0.433 |
|
1975 |
Ronald RC. Methoxymethyl ethers. An activating group for rapid and regioselective metalation Tetrahedron Letters. 16: 3973-3974. DOI: 10.1016/S0040-4039(00)91212-7 |
0.334 |
|
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