| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Access to 11β-ethynyl-androst-5-ene
|
Lecomte, Vincent
|
|
2005
|
46 |
7 |
p. 1123-1126
4 p.
|
artikel
|
| 2 |
A diversity-oriented synthetic approach to bengamides
|
Sarabia, Francisco
|
|
2005
|
46 |
7 |
p. 1131-1135
5 p.
|
artikel
|
| 3 |
A novel clathrate host allowing structural adjustment during the inclusion of 1,2-diaminoethanes
|
Yamaguchi, Koki
|
|
2005
|
46 |
7 |
p. 1087-1090
4 p.
|
artikel
|
| 4 |
Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids
|
Soloshonok, Vadim A.
|
|
2005
|
46 |
7 |
p. 1107-1110
4 p.
|
artikel
|
| 5 |
A thermally-cleavable linker for solid-phase synthesis
|
Keller, Keith A.
|
|
2005
|
46 |
7 |
p. 1181-1184
4 p.
|
artikel
|
| 6 |
Barrelene–semibullvalene rearrangement induced by visible light: synthesis of dicorannulenosemibullvalene dimethyl dicarboxylate
|
Sygula, Andrzej
|
|
2005
|
46 |
7 |
p. 1189-1192
4 p.
|
artikel
|
| 7 |
(Bromodimethyl)sulfonium bromide: an inexpensive reagent for the solvent-free, one-pot synthesis of α-aminophosphonates
|
Kudrimoti, Sucheta
|
|
2005
|
46 |
7 |
p. 1209-1210
2 p.
|
artikel
|
| 8 |
Chiral ferrocenyl diphosphines for asymmetric transfer hydrogenation of acetophenone
|
Cabou, Jérôme
|
|
2005
|
46 |
7 |
p. 1185-1188
4 p.
|
artikel
|
| 9 |
Contributors to this issue
|
|
|
2005
|
46 |
7 |
p. I-
1 p.
|
artikel
|
| 10 |
Corrigendum to “Enantioselective protonation of prochiral enolates in the asymmetric synthesis of (S)-naproxen”
|
Melgar-Fernández, Roberto
|
|
2005
|
46 |
7 |
p. 1221-1222
2 p.
|
artikel
|
| 11 |
Design and synthesis of novel ionic liquid/liquid crystals (IL2Cs) with axial chirality
|
Baudoux, Jérôme
|
|
2005
|
46 |
7 |
p. 1137-1140
4 p.
|
artikel
|
| 12 |
Diastereoselective synthesis of unsaturated 1,2-amino alcohols from α-hydroxy allyl ethers using chlorosulfonyl isocyanate
|
Kim, Ji Duck
|
|
2005
|
46 |
7 |
p. 1079-1082
4 p.
|
artikel
|
| 13 |
Domino functionalizations of the amino terminus of 6-aminopenicillanates with Ph3PCCO
|
Schobert, Rainer
|
|
2005
|
46 |
7 |
p. 1127-1130
4 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2005
|
46 |
7 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Efficient synthesis of 3-carboxylate pyrroles using microwave irradiation
|
Grassi, Giovanni
|
|
2005
|
46 |
7 |
p. 1061-1062
2 p.
|
artikel
|
| 16 |
Electronic structure of the enolate anion of chlorophyll b
|
Hynninen, Paavo H.
|
|
2005
|
46 |
7 |
p. 1145-1147
3 p.
|
artikel
|
| 17 |
Electrophilic reaction of nitric oxide with Wittig reagents
|
Liu, Zhongquan
|
|
2005
|
46 |
7 |
p. 1095-1097
3 p.
|
artikel
|
| 18 |
Facile, chemoenzymatic synthesis of the potent antiviral compound, 2-acetonylinosine
|
Gupta, Mukta
|
|
2005
|
46 |
7 |
p. 1165-1167
3 p.
|
artikel
|
| 19 |
Facile chemoselective rhodium carbenoid N–H insertion reactions: synthesis of 3-arylamino- or 3-heteroarylpiperidin-2-ones
|
Muthusamy, Sengodagounder
|
|
2005
|
46 |
7 |
p. 1063-1066
4 p.
|
artikel
|
| 20 |
Gallium(III) halide promoted synthesis of 1,3,5-triaryl- 1,5-dihalo-1,4-pentadienes
|
Yadav, J.S.
|
|
2005
|
46 |
7 |
p. 1161-1163
3 p.
|
artikel
|
| 21 |
Graphical contents list
|
|
|
2005
|
46 |
7 |
p. 1049-1059
11 p.
|
artikel
|
| 22 |
Hydrazine hydrate induced reductive cleavage of α,β-epoxy ketones: an efficient procedure for the preparation of β-hydroxy ketones
|
Salvador, Jorge A.R.
|
|
2005
|
46 |
7 |
p. 1067-1070
4 p.
|
artikel
|
| 23 |
Improved synthesis of 2,2′-dimethoxy-1,1′-binaphthyl-3,3′-diacetic acid derivatives
|
Zrig, Samia
|
|
2005
|
46 |
7 |
p. 1103-1105
3 p.
|
artikel
|
| 24 |
Instructions to contributors
|
|
|
2005
|
46 |
7 |
p. III-VI
nvt p.
|
artikel
|
| 25 |
Intramolecular [2+3]-addition of an azide to a CC double bond as a novel approach to piperazines
|
Lukina, Tatjana V.
|
|
2005
|
46 |
7 |
p. 1205-1207
3 p.
|
artikel
|
| 26 |
Lewis acid–aldehyde–solvent interactions. A computational approach for determining the critical amount of THF molecules necessary for achieving a high enantioselection in chiral oxazaborolidinone-promoted asymmetric aldol reactions
|
Fujiyama, Ryoji
|
|
2005
|
46 |
7 |
p. 1211-1215
5 p.
|
artikel
|
| 27 |
Micelle-derived polymer supports for enantioselective catalysts
|
Takizawa, Shinobu
|
|
2005
|
46 |
7 |
p. 1193-1197
5 p.
|
artikel
|
| 28 |
Microwave-assisted synthesis of 4,4′-diaminotriphenylmethanes
|
Guzmán-Lucero, D.
|
|
2005
|
46 |
7 |
p. 1119-1122
4 p.
|
artikel
|
| 29 |
Molecular mechanics-assisted crystal engineering of solid state photoreactions: application to the Yang photocyclization of α-1-norbornylacetophenone derivatives
|
Botoshansky, Mark
|
|
2005
|
46 |
7 |
p. 1141-1144
4 p.
|
artikel
|
| 30 |
Novel cyclo-dimerization of 1-tert-butoxycarbonyl-3-alkenylindole derivatives
|
Kawasaki, Ikuo
|
|
2005
|
46 |
7 |
p. 1199-1203
5 p.
|
artikel
|
| 31 |
Oxidative coupling of 2-substituted 1,2-dihydro-1-naphthols using Jones reagent: a simple entry into 3,3′-disubstituted 1,1′-binaphthyl-4,4′-diols
|
Fillion, Eric
|
|
2005
|
46 |
7 |
p. 1091-1094
4 p.
|
artikel
|
| 32 |
Practical and efficient synthesis of N-halo compounds
|
Zhong, Yong-Li
|
|
2005
|
46 |
7 |
p. 1099-1101
3 p.
|
artikel
|
| 33 |
Preparation of 2A,3A-alloepimino-2A,3A-dideoxy-β-cyclodextrin as a versatile scaffold candidate for the hetero-2A,3A-bifunctionalization
|
Fukudome, Makoto
|
|
2005
|
46 |
7 |
p. 1115-1118
4 p.
|
artikel
|
| 34 |
Preparation of advanced intermediates for the synthesis of both methyllycaconitine and racemulsonine via a common intermediate
|
Kraus, George A.
|
|
2005
|
46 |
7 |
p. 1111-1113
3 p.
|
artikel
|
| 35 |
Selective oxidation of benzylic or allylic hydroxyl group of sec-1,2-diols
|
Peng, Kun
|
|
2005
|
46 |
7 |
p. 1217-1220
4 p.
|
artikel
|
| 36 |
Sodium borohydride–iodine mediated reduction of γ-lactam carboxylic acids followed by DDQ mediated oxidative aromatisation: a facile entry to N-aryl-formylpyrroles
|
Haldar, Pranab
|
|
2005
|
46 |
7 |
p. 1071-1074
4 p.
|
artikel
|
| 37 |
Studies toward the total synthesis of di- and sesterterpenes with a dicyclopenta[a,d]cyclooctane skeleton. Construction of a versatile A/B ring building block via a ring-closing metathesis reaction and carbocationic rearrangement
|
Michalak, Karol
|
|
2005
|
46 |
7 |
p. 1149-1153
5 p.
|
artikel
|
| 38 |
Synthesis and structural revision of calafianin, a member of the spiroisoxazole family isolated from the marine sponge, Aplysina gerardogreeni
|
Ogamino, Takahisa
|
|
2005
|
46 |
7 |
p. 1083-1086
4 p.
|
artikel
|
| 39 |
Synthesis of alkenes from tertiary esters utilizing the triphenylphosphine–iodine system
|
Alvarez-Manzaneda, E.J.
|
|
2005
|
46 |
7 |
p. 1075-1077
3 p.
|
artikel
|
| 40 |
Synthesis of cyclobutanones and four-membered enol ethers by using a rearrangement reaction of enol triflates
|
Tanino, Keiji
|
|
2005
|
46 |
7 |
p. 1169-1172
4 p.
|
artikel
|
| 41 |
Three component condensations catalyzed by iodine–alumina for the synthesis of substituted 3,4-dihydropyrimidin-2(1H)-ones under microwave irradiation and solvent-free conditions
|
Saxena, Ira
|
|
2005
|
46 |
7 |
p. 1159-1160
2 p.
|
artikel
|
| 42 |
Titanocene(III) mediated radical cyclization of α-bromo carbonyl compounds: synthesis of tri-substituted tetrahydrofurans
|
Jana, Samaresh
|
|
2005
|
46 |
7 |
p. 1155-1157
3 p.
|
artikel
|
| 43 |
Total synthesis of the antitumor active pyrrolo[2,1-a]isoquinoline alkaloid (±)-crispine A
|
Knölker, Hans-Joachim
|
|
2005
|
46 |
7 |
p. 1173-1175
3 p.
|
artikel
|
| 44 |
Viehe’s salt in a novel one pot synthesis of pyrimidines
|
Kiselyov, Alexander S.
|
|
2005
|
46 |
7 |
p. 1177-1179
3 p.
|
artikel
|
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