Year |
Citation |
Score |
2010 |
MAHAL RS, WANG S, BERRISFORD KJM, PROCTER G. ChemInform Abstract: Stereoselective Additions to α,β-Epoxyaldehydes Cheminform. 27: no-no. DOI: 10.1002/chin.199638297 |
0.307 |
|
2002 |
Pepper AG, Procter G, Voyle M. Stereoselective cycloadditions of chiral acyl-nitroso compounds; selective reactions of ring-cleaved cycloadducts leading to a new approach to polyoxamic acid. Chemical Communications (Cambridge, England). 1066-7. PMID 12122667 DOI: 10.1039/B201645C |
0.461 |
|
1995 |
Ward RA, Procter G. Allylsilanes in organic synthesis; double asymmetric induction in the dihydroxylation of a chiral allylsilane Tetrahedron. 51: 12821-12836. DOI: 10.1016/S0040-4039(00)92089-6 |
0.424 |
|
1995 |
Roe MB, Whittaker M, Procter G. Studies on the synthesis of solenolide f.; a cr(ii)-mediated cyclization to form the ten-membered ring Tetrahedron Letters. 36: 8103-8106. DOI: 10.1016/0040-4039(95)01687-D |
0.321 |
|
1995 |
Daly MJ, Procter G. Allylsilanes in organic synthesis: highly stereoselective alkylation of β-silyl-γ-lactones Tetrahedron Letters. 36: 7549-7550. DOI: 10.1016/0040-4039(95)01529-9 |
0.569 |
|
1995 |
Daly MJ, Ward RA, Thompson DF, Procter G. Allylsilanes in organic synthesis; stereoselective synthesis of trans-alkene peptide isosteres Tetrahedron Letters. 36: 7545-7548. DOI: 10.1016/0040-4039(95)01528-0 |
0.497 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; palladium(0) catalyzed allylic displacement with concomitant loss of the chiral auxiliary Tetrahedron Letters. 36: 7541-7544. DOI: 10.1016/0040-4039(95)01527-2 |
0.464 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; unexpected formation of an oxazolidinone Tetrahedron Letters. 36: 7539-7540. DOI: 10.1016/0040-4039(95)01526-4 |
0.449 |
|
1995 |
Muxworthy JP, Wilkinson JA, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; hydrolytic reactions of a clyclopentadiene adduct Tetrahedron Letters. 36: 7535-7538. DOI: 10.1016/0040-4039(95)01525-6 |
0.494 |
|
1995 |
A. Ward R, Procter G. A Total Synthesis of the Natural Enantiomer of the Gastroprotective Natural Products AI-77-B and Amicoumacin C Hydrochloride Tetrahedron. 51: 12301-12318. DOI: 10.1016/0040-4020(95)00776-5 |
0.366 |
|
1995 |
Procter G, Nally J, Ordsmith NHR. β-Lactams from tetrahydro-1,2-oxazine-3,6-diones, and a labelling study of the product stereochemistry Tetrahedron. 51: 12837-12842. DOI: 10.1016/0040-4020(95)00737-S |
0.408 |
|
1994 |
Hayes JF, Mitchell MB, Procter G. A novel and efficient synthesis of a tetra-substituted imidazole Tetrahedron Letters. 35: 273-274. DOI: 10.1016/S0040-4039(00)76529-4 |
0.502 |
|
1992 |
Heneghan M, Procter G. Stereoselective Additions to Diprotected α-Aminoaldehydes Synlett. 1992: 489-490. DOI: 10.1055/S-1992-21387 |
0.371 |
|
1992 |
Ward RA, Procter G. A total synthesis of AI-77-B Tetrahedron Letters. 33: 3359-3362. DOI: 10.1016/S0040-4039(00)92088-4 |
0.361 |
|
1992 |
Beresford KJM, Howe GP, Procter G. Asymmetric synthesis via nucleophilic addition to α,β-epoxyimines Tetrahedron Letters. 33: 3355-3358. DOI: 10.1016/S0040-4039(00)92087-2 |
0.487 |
|
1992 |
Wang S, Howe GP, Mahal RS, Procter G. Stereoselective reactions of α,β-epoxy-aldehydes; the formation of "chelation controlled" products Tetrahedron Letters. 33: 3351-3354. DOI: 10.1016/S0040-4039(00)92086-0 |
0.511 |
|
1990 |
Murphy PJ, Procter G. Allylsilanes in organic synthesis; An approach to the stereoselective synthesis of units for natural product synthesis Tetrahedron Letters. 31: 1059-1062. DOI: 10.1016/S0040-4039(00)94430-7 |
0.6 |
|
1990 |
Murphy PJ, Russell AT, Procter G. Allylsilanes in organic synthesis; stereoselective preparation and reactions of functionalised β,γ-epoxysilanes Tetrahedron Letters. 31: 1055-1058. DOI: 10.1016/S0040-4039(00)94429-0 |
0.651 |
|
1990 |
Murphy PJ, Spencer JL, Procter G. Allylsilanes in organic synthesis; convenient preparation of synthetic intermediates by catalytic hydrosilation of acetylenic alcohols Tetrahedron Letters. 31: 1051-1054. DOI: 10.1016/S0040-4039(00)94428-9 |
0.505 |
|
1990 |
Morley AD, Hollinshead DM, Procter G. Stereoselective cycloadditions of acyl-nitroso compounds; an approach to carbapenem synthesis Tetrahedron Letters. 31: 1047-1050. DOI: 10.1016/S0040-4039(00)94427-7 |
0.508 |
|
1990 |
Miller A, Procter G. Stereoselective cycloadditions of chiral acyl-nitroso compounds; synthetically useful reactions of the adducts Tetrahedron Letters. 31: 1043-1046. DOI: 10.1016/S0040-4039(00)94426-5 |
0.462 |
|
1990 |
Miller A, Procter G. On the origin of the diastereoselectivity observed in cycloadditions of chiral acyl-nitroso compounds Tetrahedron Letters. 31: 1041-1042. DOI: 10.1016/S0040-4039(00)94425-3 |
0.353 |
|
1990 |
Procter G, Genin D, Challenger S. 1,6-Anhydro-β-d-glucopyranose in organic synthesis: preparation of a fragment for the synthesis of rosaramycin Carbohydrate Research. 202: 81-92. DOI: 10.1016/0008-6215(90)84072-3 |
0.459 |
|
1989 |
Miller A, Paterson TMC, Procter G. Stereoselective Cycloadditions of Chiral Acyl-Nitroso Compounds Synlett. 1989: 32-34. DOI: 10.1055/S-1989-34699 |
0.393 |
|
1988 |
Procter G, Russell AT, Murphy PJ, Tan TS, Mather AN. Epoxy-silanes in organic synthesis Tetrahedron. 44: 3953-3973. DOI: 10.1016/S0040-4020(01)86648-5 |
0.62 |
|
1987 |
Howe GP, Wang S, Procter G. Stereoselective additions to α,β-epoxy-aldehydes; the formation of "non-chelation controlled" products Tetrahedron Letters. 28: 2629-2632. DOI: 10.1016/S0040-4039(00)96166-5 |
0.48 |
|
1987 |
Russell AT, Procter G. Allylsilanes in organic synthesis; stereoselective reaction of chiral ester-allylsilanes with m-CPBA Tetrahedron Letters. 28: 2045-2048. DOI: 10.1016/S0040-4039(00)96041-6 |
0.511 |
|
1987 |
Russell AT, Procter G. Allylsilanes in organic synthesis; Stereoselective hydroxylactonisation of chiral amide-allylsilanes Tetrahedron Letters. 28: 2041-2044. DOI: 10.1016/S0040-4039(00)96040-4 |
0.485 |
|
1987 |
Murphy PJ, Procter G, Russell AT. Stereoselective aldol reactions via titanium enolates Tetrahedron Letters. 28: 2037-2039. DOI: 10.1016/S0040-4039(00)96039-8 |
0.56 |
|
1986 |
Challenger S, Procter G. Anhydro-D-glucopyranose is organic synthesis; Preparation of a fragment for a synthesis of rosaramycin Tetrahedron Letters. 27: 391-394. DOI: 10.1016/S0040-4039(00)84027-7 |
0.41 |
|
1985 |
Hodges PJ, Procter G. 1,6-Anhydroglucose in organic synthesis; preparation of fragments suitable for natural product synthesis Tetrahedron Letters. 26: 4111-4114. DOI: 10.1016/S0040-4039(00)89306-5 |
0.484 |
|
1985 |
Nally J, Ordsmith NH, Procter G. β-Lactams from tetrahydro-1,2-oxazine-3,6-diones Tetrahedron Letters. 26: 4107-4110. DOI: 10.1016/S0040-4039(00)89305-3 |
0.391 |
|
1985 |
Barnes NJ, Davidson AH, Hughes LR, Procter G. The synthesis of optically active tetrahydropyrans by the addition of a stabilised wittig reagent to pyranose sugars Journal of the Chemical Society, Chemical Communications. 1292-1294. DOI: 10.1002/Chin.198604169 |
0.456 |
|
1984 |
Tan TS, Mather AN, Procter G, Davidson AH. Allylsilane cyclisations in organic synthesis; formation of a cyclopentane via cyclisation of an epoxy-allylsilane Journal of the Chemical Society, Chemical Communications. 585-586. DOI: 10.1039/C39840000585 |
0.486 |
|
1984 |
Tan TS, Mather AN, Procter G, Davidson AH. Allylsilane Cyclizations In Organic Synthesis: Formation Of A Cyclopentane Via Cyclization Of An Epoxyallylsilane Cheminform. 15. DOI: 10.1002/Chin.198437137 |
0.493 |
|
1983 |
Batmangherlich S, Davidson AH, Procter G. The addition of carbanions to iodolactones: a stereochemically controlled approach to substituted tetrahydrofurans Tetrahedron Letters. 24: 2889-2892. DOI: 10.1016/S0040-4039(00)88051-X |
0.337 |
|
1981 |
Barnes NJ, Davidson AH, Hughes LR, Procter G, Rajcoomar V. Synthetic studies on ambruticin: Determination of the absolute stereochemistry by a chiral synthesis of the cyclopropane ring Tetrahedron Letters. 22: 1751-1754. DOI: 10.1016/S0040-4039(01)90430-7 |
0.432 |
|
1981 |
Baldwin JE, Beckwith ALJ, Davis AP, Procter G, Singleton KA. 5-Isothiazolidinonyl and 5-isoxazolidinonyl radicals. Approaches to the biogenetic-type synthesis of β-lactams Tetrahedron. 37: 2181-2189. DOI: 10.1016/S0040-4020(01)97977-3 |
0.422 |
|
1980 |
Acheson RM, Letcher RM, Procter G. Addition reactions of heterocyclic compounds. Part 72. Dimethyl acetylenedicarboxylate with 1, 2, 6, 7, 8, 9-hexahydropyrrolo[3, 2, 1-jk]carbazole Journal of the Chemical Society, Perkin Transactions 1. 535-539. DOI: 10.1039/P19800000535 |
0.373 |
|
1979 |
Acheson RM, Prince RJ, Procter G. Two novel indole rearrangements Journal of the Chemical Society, Perkin Transactions 1. 595-598. |
0.305 |
|
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