Year |
Citation |
Score |
2003 |
Mosher HS, Yanko WH, Whitmore FC. 6-Methoxy-8-nitroquinoline † Organic Syntheses. 48-48. DOI: 10.1002/0471264180.Os027.20 |
0.458 |
|
1991 |
Cheng MC, Kim K, Lin YT, Plummer JS, Talhouk J, Wang Y, You TP, Mosher HS. 3-amino-2,3-dideoxy-D-erythro-furanose derivatives Tetrahedron. 47: 4861-4868. DOI: 10.1016/S0040-4020(01)80952-2 |
0.322 |
|
1986 |
Weber JF, Talhouk JW, Nachman RJ, You TP, Halaska RC, Williams TM, Mosher HS. Methyl 2,3-dideoxy-3-nitro-D-erythro-pentofuranoside, isomers and derivatives Journal of Organic Chemistry. 51: 2702-2706. DOI: 10.1021/Jo00364A015 |
0.306 |
|
1986 |
Wu B, Mosher HS. Configuration of some para-substituted benzhydrols Journal of Organic Chemistry. 51: 1904-1906. DOI: 10.1002/Chin.198645068 |
0.328 |
|
1985 |
Makino T, Orfanopoulos M, You TP, Wu B, Mosher CW, Mosher HS. Chiral benzhydrol-2,3,4,5,6-d5 Journal of Organic Chemistry. 50: 5357-5360. DOI: 10.1021/Jo00225A067 |
0.552 |
|
1985 |
Williams TM, Mosher HS. A chiral nitronate dianion from (=d)-glyceraldehyde. Enantiospecific syntheses of 2,3-dideoxy-3-nitro furanosides and pyranosides Tetrahedron Letters. 26: 6269-6272. DOI: 10.1016/S0040-4039(01)84574-3 |
0.368 |
|
1983 |
Mosher HS, Morrison JD. Current status of asymmetric synthesis. Science (New York, N.Y.). 221: 1013-9. PMID 17736639 DOI: 10.1002/Chin.198401370 |
0.333 |
|
1981 |
Shortt AB, Mosher HS. The Reaction of P2I4 and N, N-Dimethylformamide Synthetic Communications. 11: 733-736. DOI: 10.1080/00397918108063650 |
0.325 |
|
1974 |
Anderson PH, Stephenson B, Mosher HS. Displacement reaction of neopentyl-1-d tosylate without rearrangement and optical rotatory dispersion spectra of chiral compounds with four different groups of either C3.nu. or C.inf..nu. symmetry attached to a central carbon Journal of the American Chemical Society. 96: 3171-3177. DOI: 10.1021/Ja00817A025 |
0.312 |
|
1974 |
Mosher HS. Stereochemistry of neopentyl systems Tetrahedron. 30: 1733-1745. DOI: 10.1016/S0040-4020(01)97307-7 |
0.34 |
|
1973 |
Yamaguchi S, Mosher HS. Asymmetric reductions with chiral reagents from lithium aluminum hydride and (+)-(2S,3R)-4-dimethylamino-3-methyl-1,2-diphenyl-2-butanol Journal of Organic Chemistry. 38: 1870-1877. DOI: 10.1021/Jo00950A020 |
0.3 |
|
1971 |
Biernbaum MS, Mosher HS. Asymmetric reductions. XIV. Reductions of phenyl trimethylsilyl ketone and phenyl triphenylsilyl ketone and configurational studies on the corresponding carbinols Journal of Organic Chemistry. 36: 3168-3177. DOI: 10.1021/Jo00820A020 |
0.367 |
|
1971 |
Biernbaum MS, Mosher HS. Stereochemistry of the silylcarbinol to silyl ether rearrangement Journal of the American Chemical Society. 93: 6221-6223. DOI: 10.1021/Ja00752A037 |
0.362 |
|
1971 |
Knight MH, Putkey T, Mosher HS. Bldg. Eines Benzocyclobuten-Derivates, Die Diazotierung Von 3-Amino-4-Tert.-Butyl-5-Nitro-Benzoesaeure Cheminform. 2. DOI: 10.1002/Chin.197138243 |
0.308 |
|
1968 |
Peters HM, Feigl DM, Mosher HS. Absolute configuration of substituted trifluoromethylcarbinols Journal of Organic Chemistry. 33: 4245-4250. DOI: 10.1021/Jo01275A048 |
0.328 |
|
1968 |
Blomberg C, Mosher HS. A radical process in a reaction of a grignard compound Journal of Organometallic Chemistry. 13: 519-522. DOI: 10.1016/S0022-328X(00)82781-3 |
0.325 |
|
1967 |
Singer MS, Salinger RM, Mosher HS. Kinetic study of the reduction of di-tert-butyl ketone with tert-butylmagnesium compounds Journal of Organic Chemistry. 32: 3821-3826. DOI: 10.1021/Jo01287A021 |
0.365 |
|
1964 |
MACLEOD R, PROSSER H, FIKENTSCHER L, LANYI J, MOSHER HS. ASYMMETRIC REDUCTIONS. 12. STEREOSELECTIVE KETONE REDUCTIONS BY FERMENTING YEAST. Biochemistry. 3: 838-46. PMID 14211626 DOI: 10.1021/Bi00894A020 |
0.314 |
|
1964 |
Birtwistle JS, Lee K, Morrison JD, Sanderson WA, Mosher HS. Asymmetric reductions. XI. The Grignard reagent from (+)-1-chloro-2-phenylbutane Journal of Organic Chemistry. 29: 37-40. DOI: 10.1021/Jo01024A008 |
0.341 |
|
1963 |
Cowan DO, Mosher HS. Comparison of the initial and final stages of the Grignard reduction reaction Journal of Organic Chemistry. 28: 204-206. DOI: 10.1021/Jo01036A048 |
0.513 |
|
1962 |
Cowan DO, Mosher HS. Comparison of the reactions of Grignard reagents and dialkylmagnesium compounds in addition, reduction, and enolization reactions Journal of Organic Chemistry. 27: 1-5. DOI: 10.1021/Jo01048A001 |
0.562 |
|
1962 |
Margerum JD, Miller LJ, Saito E, Brown MS, Mosher HS, Hardwick R. Phototropism of ortho-nitrobenzyl derivatives Journal of Physical Chemistry. 66: 2434-2438. DOI: 10.1021/J100818A028 |
0.305 |
|
1960 |
Burrows EP, Welch FJ, Mosher HS. Asymmetric reductions. VIII. The action of the Grignard reagent from (+)-1-chloro-2-methylbutane on cyclohexyl alkyl ketones Journal of the American Chemical Society. 82: 880-885. DOI: 10.1021/Ja01489A029 |
0.353 |
|
1960 |
MacLeod R, Welch FJ, Mosher HS. Asymmetric Reductions. VII. The Action of the Grignard reagent from (+)-1-chloro-2-methylbutane on a series of alkyl phenyl ketones Journal of the American Chemical Society. 82: 876-880. DOI: 10.1021/Ja01489A028 |
0.373 |
|
1959 |
Foley W, Welch F, LaCombe E, Mosher H. Additions and Corrections: Asymmetric Reductions. VI. The Action of the Grignard Reagent from (+)-1-Chloro-2-methylbutane on a Series of Alkyl t-Butyl Ketones. Journal of the American Chemical Society. 81: 6535-6537. DOI: 10.1021/Ja01533A643 |
0.311 |
|
1956 |
Mosher HS, Stevenot JE, Kimble DO. Asymmetric reductions. IV. The action of the Grignard reagent from (+)-2-methylbutyl chloride on 2,2,2-trifluoroacetophenone Journal of the American Chemical Society. 78: 4374-4376. DOI: 10.1021/Ja01598A049 |
0.305 |
|
1956 |
Mosher HS, Parker ED. Asymmetric reductions. III. The action of (+)-2-methylbutylmagnesium chloride on substituted benzophenones Journal of the American Chemical Society. 78: 4081-4082. DOI: 10.1021/Ja01597A059 |
0.32 |
|
1955 |
Mosher HS, Look M. Heterocyclic basic compounds. XVI. 4-chloropico-linic acid and some of its derivatives Journal of Organic Chemistry. 20: 283-286. DOI: 10.1021/Jo01121A002 |
0.33 |
|
1954 |
Spalding DP, Chapin EC, Mosher HS. Heterocyclic basic compounds. XV. Benzacridine derivatives Journal of Organic Chemistry. 10: 357-364. DOI: 10.1021/Jo01368A011 |
0.332 |
|
1953 |
Mosher HS, Frankel MB, Gregory M. Heterocyclic diphenylmethane derivatives Journal of the American Chemical Society. 75: 5326-5328. DOI: 10.1021/Ja01117A054 |
0.323 |
|
1953 |
Mosher HS, Cornell J, Stafford OL, Roe T. Synthesis of Piperazines by Reductive Cyclization1,2 Journal of the American Chemical Society. 75: 4949-4951. DOI: 10.1021/Ja01116A020 |
0.303 |
|
1951 |
Mosher HS, Tessieri JE. Heterocyclic basic compounds. XIV. 4-phenyl-4-(3-pyridyl)-6-dimethylamino-3-hexanone Journal of the American Chemical Society. 73: 4925-4927. DOI: 10.1021/Ja01154A135 |
0.327 |
|
1951 |
Mosher HS, Mooney WT. The reduction of trimethylacetonitrile with Grignard reagents Journal of the American Chemical Society. 73: 3948-3949. DOI: 10.1021/Ja01152A114 |
0.304 |
|
1951 |
Gray FW, Mosher HS, Whitmore FC, Oakwood TS. Methyl β-(m-Chloroanilino)-acrylate Journal of the American Chemical Society. 73: 3577-3578. DOI: 10.1021/Ja01152A008 |
0.458 |
|
1950 |
Spalding DP, Mosher HS, Whitmore FC. Heterocyclic basic compounds. XIII. 4-aminocoumarin derivatives Journal of the American Chemical Society. 72: 5338-5339. DOI: 10.1021/Ja01167A537 |
0.529 |
|
1950 |
Clark DE, Mosher HS. Reaction of phenylmagnesium bromide with basically substituted nitriles Journal of the American Chemical Society. 72: 1026-1027. DOI: 10.1021/Ja01158A506 |
0.333 |
|
1950 |
Frankel M, Mosher HS, Whitmore FC. Addition Reactions of 1-Cyano-1,3-butadiene1,2 Journal of the American Chemical Society. 72: 81-83. DOI: 10.1021/Ja01157A023 |
0.504 |
|
1950 |
Frankel M, Mosher HS, Whitmore FC. Addition reactions of 1-cyano-1,3-butadiene Journal of the American Chemical Society. 72: 81-83. |
0.449 |
|
1949 |
Miller AL, Mosher HS, Gray FW, Whitmore FC. The Sulfonation ofm-Aminophenol Journal of the American Chemical Society. 71: 3559-3560. DOI: 10.1021/Ja01178A524 |
0.431 |
|
1949 |
Conroy AE, Mosher HS, Whitmore FC. Heterocyclic basic compounds. XII. 7-Bromo-and 7-iodo-quinolines Journal of the American Chemical Society. 71: 3236-3237. DOI: 10.1021/Ja01177A504 |
0.47 |
|
1946 |
Spalding DP, Moersch GW, Mosher HS, Whitmore FC. Heterocyclic basic compounds. IX. 3,6-Dichloro-9-(1-methyl-4-diethylaminobutyl)-aminoacridine Journal of the American Chemical Society. 68: 1596-1598. PMID 20994993 |
0.475 |
|
1946 |
Whitmore FC, Mosher HS, Spalding DP, Taylor RB, Moersch GW, Yanko WH. Addition of secondary amines to dibromopropanol Journal of the American Chemical Society. 68: 531-532. DOI: 10.1021/Ja01207A516 |
0.454 |
|
1945 |
Weisel CA, Taylor RB, Mosher HS, Whitmore FC. Substituted β-aminopropionic esters Journal of the American Chemical Society. 67: 1071-1072. DOI: 10.1021/Ja01223A012 |
0.421 |
|
1945 |
Weisel CA, Mosher HS, Whitmore FC. Basically substituted aliphatic derivatives of urea Journal of the American Chemical Society. 67: 1055-1056. DOI: 10.1021/Ja01223A005 |
0.486 |
|
1945 |
Yanko WH, Mosher HS, Whitmore FC. Heterocyclic basic compounds. III. Basically-substituted quinoline derivatives Journal of the American Chemical Society. 67: 664-668. DOI: 10.1021/Ja01220A048 |
0.494 |
|
1945 |
Mosher HS, Whitmore FC. Heterocyclic basic compounds. II. Aminoalkylamino-s-triazines Journal of the American Chemical Society. 67: 662-664. DOI: 10.1021/Ja01220A047 |
0.442 |
|
1945 |
Whitmore FC, Mosher HS, Goldsmith DPJ, Rytina AW. Heterocyclic basic compounds. I. 2-Aminoalkylamino-pyridines Journal of the American Chemical Society. 67: 393-395. |
0.469 |
|
1944 |
Whitmore FC, Mosher HS, Adams RR, Taylor RB, Chapin EC, Weisel C, Yanko W. Basically substituted aliphatic nitriles and their catalytic reduction to amines Journal of the American Chemical Society. 66: 725-731. DOI: 10.1021/Ja01233A019 |
0.492 |
|
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