Year |
Citation |
Score |
1977 |
Burgstahler AW, Weigel LO, Sanders ME, Shaefer CG, Bell WJ, Vuturo SB. Synthesis and activity of 29-hydroxy-3,11-dimethyl-2-nonacosanone, component B of the German cockroach sex pheromone. The Journal of Organic Chemistry. 42: 566-8. PMID 556765 DOI: 10.1002/Chin.197726380 |
0.355 |
|
1976 |
Burgstahler AW, Boger DL, Naik NC. Synthesis and chiroptical properties of some asymmetric planar cisoid dienes Tetrahedron. 32: 309-315. DOI: 10.1016/0040-4020(76)80042-7 |
0.392 |
|
1976 |
Burgstahler AW, Boger DL, Naik NC. Synthesis and chiroptical properties of some asymmetric planar dienes. Tetrahedron. 32: 2474. |
0.396 |
|
1975 |
Burgstahler AW, Weigel LO, Bell WJ, Rust MK. Synthesis of 3,11-dimethyl-2-nonacosanone, a contact courting pheromone of the German cockroach. The Journal of Organic Chemistry. 40: 3456-8. PMID 1185318 DOI: 10.1021/JO00911A039 |
0.458 |
|
1973 |
Burgstahler AW, Widiger GN. Synthesis of spiro ketals from Japanese hops Journal of Organic Chemistry. 38: 3652-3653. DOI: 10.1021/Jo00960A056 |
0.55 |
|
1973 |
Burgstahler AW, Kroeger HW. An Alternative Route to Yomogi Alcohol Synthetic Communications. 3: 211-212. DOI: 10.1002/Chin.197346462 |
0.339 |
|
1972 |
Burgstahler AW, Walker DE, Kuebrich JP, Schowen RL. Synthesis of benzaldehyde-formyl-d from benzil The Journal of Organic Chemistry. 37: 1272-1273. DOI: 10.1021/Jo00973A048 |
0.383 |
|
1972 |
Burgstahler AW, Walker DE, Kuebrich JP, Schowen RL. A convenient synthesis of benzaldehyde-formyl-d from benzil Journal of Organic Chemistry. 37: 1272-1273. DOI: 10.1021/Jo00796A923 |
0.392 |
|
1972 |
Burgstahler AW, Walker DE, Kuebrich JP, Schowen RL. Correction. A Convenient Synthesis of Benzaldehyde-formyl-dfrom Benzil The Journal of Organic Chemistry. 37: 3754-3754. DOI: 10.1021/Jo00796A625 |
0.52 |
|
1971 |
Rowe JW, Nagasampagi BA, Burgstahler AW, Fitzsimmons JW. Derivatives of nordehydroabietane from pine bark Phytochemistry. 10: 1647-1651. DOI: 10.1016/0031-9422(71)85040-9 |
0.376 |
|
1970 |
Tamelen EEV, Shamma M, Burgstahler AW, Wolinsky J, Tamm R, Aldrich PE. Totalsynth. Von Yohimbin Cheminform. 1. DOI: 10.1002/Chin.197013371 |
0.446 |
|
1969 |
van Tamelen EE, Shamma M, Burgstahler AW, Wolinsky J, Tamm R, Aldrich PE. Total synthesis of yohimbine. Journal of the American Chemical Society. 91: 7315-33. PMID 5358617 DOI: 10.1021/Ja01054A021 |
0.739 |
|
1969 |
Burgstahler AW, Groginsky CM. Rearrangement of 1-Vinyl-2-(1-Hexenyl) Cyclopropanes. Synthesis of (+-)-Dictyopterene A Transactions of the Kansas Academy of Science. 72: 486. DOI: 10.2307/3627649 |
0.559 |
|
1969 |
Burgstahler AW, Marx JN. Synthesis of fichtelite and related derivatives of abietane Journal of Organic Chemistry. 34: 1562-1566. DOI: 10.1021/Jo01258A006 |
0.685 |
|
1969 |
Burgstahler AW, Marx JN, Zinkel DF. Structure and stereochemistry of reduction products of abietic-type resin acids Journal of Organic Chemistry. 34: 1550-1561. DOI: 10.1021/Jo01258A005 |
0.59 |
|
1969 |
Worden LR, Burgstahler AW, Kaufman KD, Weis JA, Schaaf TK. Benzodifurans. I. The synthesis of benzo[1,2‐b:5,4‐b]difuran and some methyl analogs Journal of Heterocyclic Chemistry. 6: 191-198. DOI: 10.1002/Jhet.5570060208 |
0.385 |
|
1968 |
Burgstahler AW, Barkhurst RC. Preparation of Leuconic Acid from Inositol Transactions of the Kansas Academy of Science. 71: 150. DOI: 10.2307/3627366 |
0.323 |
|
1968 |
Burgstahler AW, Sticker RE. Studies in the pinane series Tetrahedron. 24: 2435-2442. DOI: 10.1016/S0040-4020(01)82516-3 |
0.322 |
|
1966 |
Burgstahler AW, Lewis TB, Abdel-Rahman MO. Products from the base-catalyzed chlorination of phenol. A new synthesis of (±)-caldariomycin Journal of Organic Chemistry. 31: 3516-3522. DOI: 10.1021/Jo01349A012 |
0.363 |
|
1965 |
Burgstahler AW, Malfer DJ, Abdel-Rahman MO. Synthesis and spectral properties of 2,6-dimethyl-t-butylbenzene Tetrahedron Letters. 6: 1625-1626. DOI: 10.1016/S0040-4039(01)84102-2 |
0.37 |
|
1964 |
BURGSTAHLER AW, TROLLOPE ML, AIMAN CE. SYNTHESIS OF 4-METHYLENE-DL-PROLINE: A NATURALLY OCCURRING RACEMIC AMINO-ACID. Nature. 202: 388-9. PMID 14158102 DOI: 10.1038/202388B0 |
0.408 |
|
1964 |
Burgstahler AW, Trollope ML, Aiman CE. Synthesis of 4-methylene-DL-proline: A naturally occurring racemic amino-acid [14] Nature. 202: 388-389. DOI: 10.1038/202388b0 |
0.334 |
|
1964 |
Chien PL, McEwen WE, Burgstahler AW, Iyer NT. Synthesis of chonemorphine stereoisomers Journal of Organic Chemistry. 29: 315-318. DOI: 10.1021/Jo01025A015 |
0.559 |
|
1964 |
Burgstahler AW, Worden LR. The synthesis of abietadienoic acids from dehydroabietic acid Journal of the American Chemical Society. 86: 96-101. DOI: 10.1021/Ja01055A022 |
0.39 |
|
1964 |
Burgstahler AW, Abdel-Rahman MO, Chien PL. Synthesis and properties of 3,4-di-t-butylphenol Tetrahedron Letters. 5: 61-64. DOI: 10.1016/S0040-4039(01)89323-0 |
0.371 |
|
1964 |
Burgstahler AW, Marx JN. The synthesis and stereochemistry of fichtelite Tetrahedron Letters. 5: 3333-3338. DOI: 10.1016/0040-4039(64)83095-1 |
0.721 |
|
1963 |
Burgstahler AW, Worden LR, Lewis TB. Direct reduction of carboxylic acids to aldehydes by lithium in ethylamine Journal of Organic Chemistry. 28: 2918-2919. DOI: 10.1021/Jo01045A532 |
0.357 |
|
1963 |
Burgstahler AW, Abdel-Rahman MO. The synthesis of o-Di-t-butylbenzene by classical reaction methods Journal of the American Chemical Society. 85: 173-180. DOI: 10.1021/Ja00885A015 |
0.32 |
|
1962 |
Burgstahler AW, Nordin IC. Angular Alkylation by the Claisen Rearrangement1 Transactions of the Kansas Academy of Science. 65: 39. DOI: 10.2307/3626467 |
0.331 |
|
1961 |
Burgstahler A, Wetmore D. Notes- Lactonization of 3-Hydroxy-3,4,4-trimethylpentanoic Acid Journal of Organic Chemistry. 26: 3516-3518. DOI: 10.1021/Jo01067A608 |
0.313 |
|
1961 |
Burgstahler AW, Worden LR. The Synthesis Of Abietic Acid From Dehydroabietic Acid Journal of the American Chemical Society. 83: 2587-2588. DOI: 10.1021/Ja01472A043 |
0.39 |
|
1961 |
Burgstahler AW, Nordin IC. Stereospecific angular alkylation. A new application of the Claisen rearrangement Journal of the American Chemical Society. 83: 198-206. DOI: 10.1021/Ja01462A039 |
0.3 |
|
1960 |
Burgstahler A, Aiman C. Correction. A Direct Synthesis of DL-Baikiain Journal of Organic Chemistry. 25: 2263-2263. DOI: 10.1021/Jo01082A642 |
0.486 |
|
1960 |
Burgstahler AW, Aiman CE. A direct synthesis of DL-baikiain Journal of Organic Chemistry. 25: 489-492. DOI: 10.1021/Jo01074A001 |
0.507 |
|
1960 |
Burgstahler AW, Bithos ZJ. Synthetic applications of hexahydrogallic acid. I. A new route to emetine Journal of the American Chemical Society. 82: 5466-5474. DOI: 10.1021/Ja01505A040 |
0.346 |
|
1959 |
Burgstahler AW, Mosettig E. The total synthesis of dl-C-17 oxygenated anthrasteroids Journal of the American Chemical Society. 81: 3697-3701. DOI: 10.1021/Ja01523A051 |
0.334 |
|
1959 |
Burgstahler AW, Nordin IC. Stereospecific introduction of angular substituents by the Claisen rearrangement [7] Journal of the American Chemical Society. 81: 3151. DOI: 10.1021/Ja01521A064 |
0.332 |
|
1959 |
Burgstahler AW, Bithos ZJ. The Synthesis Of Emetine From Hexahydrogallic Acid Journal of the American Chemical Society. 81: 503-504. DOI: 10.1021/Ja01511A063 |
0.47 |
|
1959 |
Burgstahler AW, Bithos ZJ. The synthesis of emetine from hexahydrogallic acid [3] Journal of the American Chemical Society. 81: 503-504. |
0.374 |
|
1958 |
Van Tamelen EE, Shamma M, Burgstahler AW, Wolinsky J, Tamm R, Aldrich PE. The total synthesis of yohimbine [4] Journal of the American Chemical Society. 80: 5006-5007. |
0.721 |
|
1955 |
Stork G, Burgstahler AW. The stereochemistry of polyene cyclization Journal of the American Chemical Society. 77: 5068-5077. |
0.37 |
|
1953 |
Stork G, Van Tamelen EE, Friedman LJ, Burgstahler AW. A stereospecific synthesis of cantharidin Journal of the American Chemical Society. 75: 384-392. |
0.724 |
|
1951 |
Stork G, Van Tamelen EE, Friedman LJ, Burgstahler AW. Cantharidin. A stereospecific total synthesis [8] Journal of the American Chemical Society. 73: 4501. |
0.478 |
|
1949 |
Eliel EL, Burgstahler AW. Synthesis of methyl phthalaldehydate and phthalaldehydic acid by the Rosenmund reduction Journal of the American Chemical Society. 71: 2251-2252. |
0.314 |
|
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