| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A catalytic asymmetric anti-selective nitroaldol reaction with a neodymium–sodium heterobimetallic complex
|
Nitabaru, Tatsuya
|
|
2008
|
49 |
2 |
p. 272-276
5 p.
|
artikel
|
| 2 |
Acceleration effect of allylic hydroxy group on ring-closing enyne metathesis of terminal alkynes: scope and application to the synthesis of isofagomine
|
Imahori, Tatsushi
|
|
2008
|
49 |
2 |
p. 265-268
4 p.
|
artikel
|
| 3 |
A concise approach to (+)-1-epi-castanospermine
|
Wu, Tian-Jun
|
|
2008
|
49 |
2 |
p. 383-386
4 p.
|
artikel
|
| 4 |
An efficient synthesis of N-arylated, orthogonally protected racemic aspartates
|
Luo, Guanglin
|
|
2008
|
49 |
2 |
p. 296-299
4 p.
|
artikel
|
| 5 |
A new easily accessible chiral phosphite–phosphoramidite ligand based on 2-anilinoethanol and R-BINOL moieties for Rh-catalyzed asymmetric olefin hydrogenation
|
Kostas, Ioannis D.
|
|
2008
|
49 |
2 |
p. 331-334
4 p.
|
artikel
|
| 6 |
A new strategy for the preparation of heterocyclic β-amino esters: orthogonally protected β-amino esters with a piperidine skeleton
|
Kiss, Loránd
|
|
2008
|
49 |
2 |
p. 339-342
4 p.
|
artikel
|
| 7 |
A new synthesis of potent antitumor saponin OSW-1 via Wittig rearrangement
|
Tsubuki, Masayoshi
|
|
2008
|
49 |
2 |
p. 229-232
4 p.
|
artikel
|
| 8 |
An improved synthesis of α-phosphonoenamines based on a modified Peterson olefination
|
McNulty, James
|
|
2008
|
49 |
2 |
p. 281-285
5 p.
|
artikel
|
| 9 |
A pentacyclic condensation product from 2,4-dimethyl-7-nitro-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acid
|
Ilaš, Janez
|
|
2008
|
49 |
2 |
p. 222-225
4 p.
|
artikel
|
| 10 |
Base-free monosulfonylation of amines using tosyl or mesyl chloride in water
|
Kamal, Ahmed
|
|
2008
|
49 |
2 |
p. 348-353
6 p.
|
artikel
|
| 11 |
Boronic acid-appended bis-viologens as a new family of viologen quenchers for glucose sensing
|
Sharrett, Zachary
|
|
2008
|
49 |
2 |
p. 300-304
5 p.
|
artikel
|
| 12 |
Conformational control of molecular tweezers containing a disulfide bond by redox reactions
|
Iwamoto, Hajime
|
|
2008
|
49 |
2 |
p. 277-280
4 p.
|
artikel
|
| 13 |
Construction of the 3-prenyl-4-oxa-tricyclo[4.3.1.03,7]dec-8-en-2-one core of caged xanthonoid natural products via tandem Wessely oxidation–intramolecular [4+2] cycloaddition
|
Mehta, Goverdhan
|
|
2008
|
49 |
2 |
p. 318-322
5 p.
|
artikel
|
| 14 |
Cucurbit[7]uril stabilization of a diarylmethane carbocation in aqueous solution
|
Wang, Ruibing
|
|
2008
|
49 |
2 |
p. 311-314
4 p.
|
artikel
|
| 15 |
Determination of the absolute configuration of the male aggregation pheromone, 2-methyl-6-(4′-methylenebicyclo[3.1.0]hexyl)hept-2-en-1-ol, of the stink bug Erysarcoris lewisi (Distant) as 2Z,6R,1′S,5′S by its synthesis
|
Mori, Kenji
|
|
2008
|
49 |
2 |
p. 354-357
4 p.
|
artikel
|
| 16 |
Editorial board
|
|
|
2008
|
49 |
2 |
p. IFC-
1 p.
|
artikel
|
| 17 |
Electrophilic cyclization of 4-thio-but-2-yn-1-ols via 1,2-migration of the thio group: efficient synthesis of 2,4-dihalo-3-thio-substituted furans
|
Zhou, Hongwei
|
|
2008
|
49 |
2 |
p. 226-228
3 p.
|
artikel
|
| 18 |
Enantioselective alkynylation to aldimines catalyzed by chiral 2,2′-di(2-aminoaryloxy)-1,1′-binaphthyl-copper(I) complexes
|
Hatano, Manabu
|
|
2008
|
49 |
2 |
p. 379-382
4 p.
|
artikel
|
| 19 |
Enantioselective total synthesis of (−)-tetrahydrolipstatin using Oppolzer’s sultam directed aldol reaction
|
Kumaraswamy, G.
|
|
2008
|
49 |
2 |
p. 327-330
4 p.
|
artikel
|
| 20 |
First synthesis of oxa-analogous isoindigo-N-glycosides
|
Libnow, Stefanie
|
|
2008
|
49 |
2 |
p. 289-291
3 p.
|
artikel
|
| 21 |
Formal synthesis of (−)-morphine from d-glucal based on the cascade Claisen rearrangement
|
Tanimoto, Hiroki
|
|
2008
|
49 |
2 |
p. 358-362
5 p.
|
artikel
|
| 22 |
Four new colchicinoids, gloriosamines A–D, from Gloriosa rothschildiana
|
Kitajima, Mariko
|
|
2008
|
49 |
2 |
p. 257-260
4 p.
|
artikel
|
| 23 |
From theoretical calculations to the enantioselective synthesis of a 1,3,4-trisubstituted Gly-derived 2-azetidinone
|
Pérez-Faginas, Paula
|
|
2008
|
49 |
2 |
p. 215-218
4 p.
|
artikel
|
| 24 |
Graphical contents list
|
|
|
2008
|
49 |
2 |
p. 203-214
12 p.
|
artikel
|
| 25 |
Green diastereoselective synthesis of highly functionalised trifluoromethylated γ-lactone phosphonate esters bearing a thioester or ketothiophene
|
Rostami Charati, Faramarz
|
|
2008
|
49 |
2 |
p. 343-347
5 p.
|
artikel
|
| 26 |
Greener and rapid access to bio-active heterocycles: room temperature synthesis of pyrazoles and diazepines in aqueous medium
|
Polshettiwar, Vivek
|
|
2008
|
49 |
2 |
p. 397-400
4 p.
|
artikel
|
| 27 |
Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands
|
Maayan, Galia
|
|
2008
|
49 |
2 |
p. 335-338
4 p.
|
artikel
|
| 28 |
Highly efficient indium-catalyzed chemoselective allylation–etherification and reductive etherification of aromatic aldehydes with functional silanes
|
Yang, Ming-Song
|
|
2008
|
49 |
2 |
p. 253-256
4 p.
|
artikel
|
| 29 |
Highly selective acylation of ferrocene using microfluidic chip reactor
|
Hu, Rui-Jun
|
|
2008
|
49 |
2 |
p. 387-389
3 p.
|
artikel
|
| 30 |
(IBC)Guide to Authors (2006)
|
|
|
2008
|
49 |
2 |
p. IBC-
1 p.
|
artikel
|
| 31 |
Intramolecular thermal allenyne [2+2] cycloadditions: facile construction of the 5–6–4 ring core of sterpurene
|
Ovaska, Timo V.
|
|
2008
|
49 |
2 |
p. 376-378
3 p.
|
artikel
|
| 32 |
Microwave-assisted protocols for the expedited synthesis of pyrazolo[1,5-a] and [3,4-d]pyrimidines
|
Daniels, R. Nathan
|
|
2008
|
49 |
2 |
p. 305-310
6 p.
|
artikel
|
| 33 |
Microwave-assisted synthesis of non-substituted tripyrrane, tetrapyrrane and pentapyrrane
|
Saltsman, Irena
|
|
2008
|
49 |
2 |
p. 247-249
3 p.
|
artikel
|
| 34 |
New BODIPY–triazine based tripod fluorescent systems
|
Qi, Xin
|
|
2008
|
49 |
2 |
p. 261-264
4 p.
|
artikel
|
| 35 |
Palladium-catalyzed Heck reaction under thermomorphic mode
|
Lu, Norman
|
|
2008
|
49 |
2 |
p. 371-375
5 p.
|
artikel
|
| 36 |
Practical method for the synthesis of polysilanes using Mg and Lewis acid system
|
Kashimura, Shigenori
|
|
2008
|
49 |
2 |
p. 269-271
3 p.
|
artikel
|
| 37 |
Preparation of 3-substituted-2-pyridin-2-ylindoles: regioselectivity of Larock’s indole annulation with 2-alkynylpyridines
|
Roschangar, Frank
|
|
2008
|
49 |
2 |
p. 363-366
4 p.
|
artikel
|
| 38 |
Progress towards the synthesis of papuaforin A: selective formation of α-bromoenones from silyl enol ethers
|
Kraus, George A.
|
|
2008
|
49 |
2 |
p. 286-288
3 p.
|
artikel
|
| 39 |
Radical chain reactions using THP as a solvent
|
Yasuda, Hiroshi
|
|
2008
|
49 |
2 |
p. 367-370
4 p.
|
artikel
|
| 40 |
Reactive diene for synthesis of substituted catechols
|
Compton, Benjamin J.
|
|
2008
|
49 |
2 |
p. 219-221
3 p.
|
artikel
|
| 41 |
Spectroscopic binding studies of novel fluorescent distamycin derivatives
|
Tkadlecová, Marcela
|
|
2008
|
49 |
2 |
p. 323-326
4 p.
|
artikel
|
| 42 |
Stereocontrolled approach to 1-azabicyclo[4.1.0]heptanes: application to the synthesis of trans-2,6-disubstituted piperidines
|
Wynne, Emma L.
|
|
2008
|
49 |
2 |
p. 250-252
3 p.
|
artikel
|
| 43 |
Stereospecific synthesis of the sex pheromone of the passionvine mealybug, Planococcus minor
|
Millar, Jocelyn G.
|
|
2008
|
49 |
2 |
p. 315-317
3 p.
|
artikel
|
| 44 |
Syntheses of epi-aigialomycin D and deoxy-aigialomycin C via a diastereoselective ring closing metathesis macrocyclization protocol
|
Bajwa, Naval
|
|
2008
|
49 |
2 |
p. 390-393
4 p.
|
artikel
|
| 45 |
Synthesis and metal-binding studies of a novel pyrene discotic
|
Jradi, Fadi M.
|
|
2008
|
49 |
2 |
p. 238-242
5 p.
|
artikel
|
| 46 |
Synthesis of partially reduced ferrocenylphenanthrenes from 2-oxobenzo[h]chromenes through C–C insertion
|
Pratap, Ramendra
|
|
2008
|
49 |
2 |
p. 394-396
3 p.
|
artikel
|
| 47 |
Synthesis of the DE-ring of goniodomin A and prediction of its natural relative stereochemistry
|
Katagiri, Takahiro
|
|
2008
|
49 |
2 |
p. 233-237
5 p.
|
artikel
|
| 48 |
Thio-functionalised glucosinolates: unexpected transformation of desulfoglucoraphenin
|
Iori, Renato
|
|
2008
|
49 |
2 |
p. 292-295
4 p.
|
artikel
|
| 49 |
Unusual conversion of substituted-3-formylchromones to 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones: a facile and efficient route to novel 1,2,4-dithiazoles
|
Raj, Tilak
|
|
2008
|
49 |
2 |
p. 243-246
4 p.
|
artikel
|
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