| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A convenient methodology for the chemoselective reduction of a wide variety of functionalized alkenes
|
Babler, James H.
|
|
2010
|
51 |
2 |
p. 439-441
3 p.
|
artikel
|
| 2 |
A facile approach for the synthesis of 14-aryl- or alkyl-14H-dibenzo[a,j]xanthenes under solvent-free condition
|
Kumar, Ram
|
|
2010
|
51 |
2 |
p. 442-445
4 p.
|
artikel
|
| 3 |
AlCl3 as a powerful catalyst for the one-pot preparation of 1,1,3-triheteroaryl compounds
|
Shiri, Morteza
|
|
2010
|
51 |
2 |
p. 264-268
5 p.
|
artikel
|
| 4 |
Alkoxide-induced nucleophilic trifluoromethylation using diethyl trifluoromethylphosphonate
|
Cherkupally, Prabhakar
|
|
2010
|
51 |
2 |
p. 252-255
4 p.
|
artikel
|
| 5 |
A modified Curtius reaction: an efficient and simple method for direct isolation of free amine
|
Ma, Bin
|
|
2010
|
51 |
2 |
p. 385-386
2 p.
|
artikel
|
| 6 |
An easy access to pyrimidine-fused azocine derivatives by thiophenol-mediated radical cyclization via 8-endo-trig mode
|
Majumdar, K.C.
|
|
2010
|
51 |
2 |
p. 348-350
3 p.
|
artikel
|
| 7 |
A novel access to bisformylated pyrroles via decarboxylation of N-aryl-γ-lactam-carboxylic acids under Vilsmeier reaction conditions
|
Barman, Gopa
|
|
2010
|
51 |
2 |
p. 297-300
4 p.
|
artikel
|
| 8 |
A short route to the synthesis of pyrroloacridines via Ullmann–Goldberg condensation
|
Meesala, Ramu
|
|
2010
|
51 |
2 |
p. 422-424
3 p.
|
artikel
|
| 9 |
A simple and highly effective oxidative chlorination protocol for the preparation of arenesulfonyl chlorides
|
Pu, Yu-Ming
|
|
2010
|
51 |
2 |
p. 418-421
4 p.
|
artikel
|
| 10 |
A simple method for the oxidation of α-amino acid esters to α-oximino esters
|
Wu, Lisa Y.
|
|
2010
|
51 |
2 |
p. 402-403
2 p.
|
artikel
|
| 11 |
A simplified [11C]phosgene synthesis
|
Bramoullé, Yann
|
|
2010
|
51 |
2 |
p. 313-316
4 p.
|
artikel
|
| 12 |
Asymmetric organocatalytic Michael-type reaction of phosphorus ylides to nitroolefins: synthesis of γ-nitro-β-aryl-α-methylene carboxylic esters
|
Allu, Suresh
|
|
2010
|
51 |
2 |
p. 446-448
3 p.
|
artikel
|
| 13 |
A two-step synthesis of allylic syn 1,3-diols via an intramolecular oxa-Michael reaction followed by a modified Julia olefination
|
Oriez, Raphaël
|
|
2010
|
51 |
2 |
p. 256-258
3 p.
|
artikel
|
| 14 |
Carbohydrate-based spiro bis(isoxazolines): synthesis and evaluation in asymmetric catalysis
|
Goyard, David
|
|
2010
|
51 |
2 |
p. 374-377
4 p.
|
artikel
|
| 15 |
Chiral carbene approach to gold-catalyzed asymmetric cyclization of 1,6-enynes
|
Matsumoto, Yasumasa
|
|
2010
|
51 |
2 |
p. 404-406
3 p.
|
artikel
|
| 16 |
Copper-catalyzed addition of water affording highly substituted furan and unusual formation of naphthofuran ring from 3-(1-alkenyl)-2-alkene-1-al
|
Jana, Rathin
|
|
2010
|
51 |
2 |
p. 273-276
4 p.
|
artikel
|
| 17 |
Copper(0) in the Ullmann heterocycle-aryl ether synthesis of 4-phenoxypyridine using multimode microwave heating
|
Benaskar, Faysal
|
|
2010
|
51 |
2 |
p. 248-251
4 p.
|
artikel
|
| 18 |
Corrigendum to “FeCl3-catalyzed functionalization of monoterpenes via hydroalkylation of unactivated alkenes” [Tetrahedron Lett. 50 (2009) 5783]
|
Yadav, J.S.
|
|
2010
|
51 |
2 |
p. 457-
1 p.
|
artikel
|
| 19 |
Critical importance of leaving group ‘softness’ in nucleophilic ring closure reactions of ambident anions to 1,2-diazetidines
|
Brown, Michael J.
|
|
2010
|
51 |
2 |
p. 382-384
3 p.
|
artikel
|
| 20 |
Cross coupling of 3-bromopyridine and sulfonamides (R1NHSO2R2·R1 =H, Me, alkyl; R2 =alkyl and aryl) catalyzed by CuI/1,3-di(pyridin-2-yl)propane-1,3-dione
|
Han, Xiaojun
|
|
2010
|
51 |
2 |
p. 360-362
3 p.
|
artikel
|
| 21 |
Cycloaddition of trifluoromethyl azafulvenium methides: synthesis of new trifluoromethylpyrrole-annulated derivatives
|
Nunes, Cláudio M.
|
|
2010
|
51 |
2 |
p. 411-414
4 p.
|
artikel
|
| 22 |
Diastereoselective synthesis of spiro-functionalized tetraalkyl benzoisoquinopyrrolonaphthyridine-tetracarboxylates from isoquinoline, dialkyl acetylenedicarboxylates, and indane-1,3-dione
|
Yavari, Issa
|
|
2010
|
51 |
2 |
p. 396-398
3 p.
|
artikel
|
| 23 |
Double Michael addition of dithiols to acetylenic carbonyl compounds under the influence of molecular sieve and dimethyl sulfoxide
|
Kakinuma, Tomoko
|
|
2010
|
51 |
2 |
p. 290-292
3 p.
|
artikel
|
| 24 |
Editorial board
|
|
|
2010
|
51 |
2 |
p. IFC-
1 p.
|
artikel
|
| 25 |
Efficient synthesis of chiral C 2-symmetric diamines via allylboration of bis-N,N′-metallodiimines
|
Ramachandran, P. Veeraraghavan
|
|
2010
|
51 |
2 |
p. 332-336
5 p.
|
artikel
|
| 26 |
Enzymatic synthesis of (S)-glutaric acid monoesters aided by molecular docking
|
Wang, Bo
|
|
2010
|
51 |
2 |
p. 309-312
4 p.
|
artikel
|
| 27 |
Facile nucleophilic fluorination of primary alkyl halides using tetrabutylammonium fluoride in a tert-alcohol medium
|
Kim, Dong Wook
|
|
2010
|
51 |
2 |
p. 432-434
3 p.
|
artikel
|
| 28 |
First example of FeCl3-catalyzed alkylation of indoles with pinenes
|
Yadav, J.S.
|
|
2010
|
51 |
2 |
p. 244-247
4 p.
|
artikel
|
| 29 |
Fullerenyl azide: synthesis and reactivity
|
Jiang, Zhongping
|
|
2010
|
51 |
2 |
p. 415-417
3 p.
|
artikel
|
| 30 |
Gold-catalyzed C–S bond formation from thiols
|
Jean, Mickaël
|
|
2010
|
51 |
2 |
p. 378-381
4 p.
|
artikel
|
| 31 |
Graphical contents list
|
|
|
2010
|
51 |
2 |
p. 213-229
17 p.
|
artikel
|
| 32 |
Hg cathode-free electrochemical detosylation of N,N-disubstituted p-toluenesulfonamides: mild, efficient, and selective removal of N-tosyl group
|
Senboku, Hisanori
|
|
2010
|
51 |
2 |
p. 435-438
4 p.
|
artikel
|
| 33 |
Highly stereoselective synthesis of 2′-deoxy-β-ribonucleosides via a 3′-(N-acetyl)-glycyl-directing group
|
Liu, Zhaogui
|
|
2010
|
51 |
2 |
p. 240-243
4 p.
|
artikel
|
| 34 |
High-pressure-promoted Fmoc-aminoacylation of N-ethylcysteine: preparation of key devices for the solid-phase synthesis of peptide thioesters
|
Nakahara, Yuko
|
|
2010
|
51 |
2 |
p. 407-410
4 p.
|
artikel
|
| 35 |
(IBC)Guide to Authors (2006)
|
|
|
2010
|
51 |
2 |
p. IBC-
1 p.
|
artikel
|
| 36 |
Iminonitroso ene reactions: experimental studies on reactivity, regioselectivity, and enantioselectivity
|
Yang, Baiyuan
|
|
2010
|
51 |
2 |
p. 328-331
4 p.
|
artikel
|
| 37 |
Lanthanum-catalyzed stereoselective synthesis of vinyl sulfides and selenides
|
Reddy, V. Prakash
|
|
2010
|
51 |
2 |
p. 293-296
4 p.
|
artikel
|
| 38 |
LDA-mediated domino carbolithiation reactions of vinylidenecyclopropanes with but-3-yn-2-one and 1-phenylprop-2-yn-1-one
|
Lu, Bei-Li
|
|
2010
|
51 |
2 |
p. 321-324
4 p.
|
artikel
|
| 39 |
McMurry coupling of aryl aldehydes and imino pinacol coupling mediated by Ti(O-i-Pr)4/Me3SiCl/Mg reagent
|
Okamoto, Sentaro
|
|
2010
|
51 |
2 |
p. 387-390
4 p.
|
artikel
|
| 40 |
Microwave-assisted organic synthesis of 3-substituted-imidazo[1,5-a]pyridines
|
Arvapalli, Venkata Satyanarayana
|
|
2010
|
51 |
2 |
p. 284-286
3 p.
|
artikel
|
| 41 |
N-Alkylation of poor nucleophilic amine and sulfonamide derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate
|
Martínez-Asencio, Ana
|
|
2010
|
51 |
2 |
p. 325-327
3 p.
|
artikel
|
| 42 |
Negishi coupling of 2-pyridylzinc bromide—paradigm shift in cross-coupling chemistry?
|
Coleridge, Brian M.
|
|
2010
|
51 |
2 |
p. 357-359
3 p.
|
artikel
|
| 43 |
New tricyclic geldanamycin analogues from an engineered strain of Streptomyces hygroscopicus JCM4427
|
Hong, Seong Su
|
|
2010
|
51 |
2 |
p. 351-353
3 p.
|
artikel
|
| 44 |
Norcholanic acids as substrates for recombinant 3β-hydroxysteroid dehydrogenase and progesterone 5β-reductase, enzymes of the 5β-cardenolide biosynthesis
|
Schebitz, Pia
|
|
2010
|
51 |
2 |
p. 367-370
4 p.
|
artikel
|
| 45 |
One-pot amide synthesis from allyl or benzyl halides and amines by Pd-catalysed carbonylation
|
Troisi, Luigino
|
|
2010
|
51 |
2 |
p. 371-373
3 p.
|
artikel
|
| 46 |
One-pot highly enantioselective catalytic Mannich-type reactions between aldehydes and stable α-amido sulfones: asymmetric synthesis of β-amino aldehydes and β-amino acids
|
Deiana, Luca
|
|
2010
|
51 |
2 |
p. 234-237
4 p.
|
artikel
|
| 47 |
On the catalytic duo PdCl2(PPh3)2/AuCl(PPh3) that cannot effect a Sonogashira-type reaction: a correction
|
Panda, Biswajit
|
|
2010
|
51 |
2 |
p. 301-305
5 p.
|
artikel
|
| 48 |
Oxidative bromination reaction using vanadium catalyst and aluminum halide under molecular oxygen
|
Kikushima, Kotaro
|
|
2010
|
51 |
2 |
p. 340-342
3 p.
|
artikel
|
| 49 |
Palladium- and base-free synthesis of conjugated ynones by cross-coupling reactions of alkynylboronates with acid chlorides mediated by CuCl
|
Nishihara, Yasushi
|
|
2010
|
51 |
2 |
p. 306-308
3 p.
|
artikel
|
| 50 |
Palladium-catalyzed cyclization of 1,6-enyne with 2-bromoarylaldehyde: domino sequence to [5-7-6] tricyclic ring systems
|
Fang, Xianjie
|
|
2010
|
51 |
2 |
p. 317-320
4 p.
|
artikel
|
| 51 |
Palladium-catalyzed double allylic alkylation of indole-2-hydroxamates: easy access to pyrazino[1,2-a]indole derivatives
|
Laliberté, Sébastien
|
|
2010
|
51 |
2 |
p. 363-366
4 p.
|
artikel
|
| 52 |
PhIO/Bu4NI mediated oxidative cyclization of amidoalkylation adducts for the synthesis of N-benzoyl aziridines and oxazolines
|
Fan, Renhua
|
|
2010
|
51 |
2 |
p. 453-456
4 p.
|
artikel
|
| 53 |
Rate enhancement by water in a TiCl4-mediated stereoselective vinylogous Mukaiyama aldol reaction
|
Yamaoka, Makoto
|
|
2010
|
51 |
2 |
p. 287-289
3 p.
|
artikel
|
| 54 |
Reactivity of a propiolate dimer with nucleophiles and an efficient synthesis of dimethyl α-aminoadipate
|
Zhou, Li-Hong
|
|
2010
|
51 |
2 |
p. 425-427
3 p.
|
artikel
|
| 55 |
Structure, biological activity, and a biomimetic partial synthesis of the lirofolines, novel pentacylic indole alkaloids from Tabernaemontana
|
Low, Yun-Yee
|
|
2010
|
51 |
2 |
p. 269-272
4 p.
|
artikel
|
| 56 |
Synthesis and applications of a chiral-oxygenated 3-chloro-3,6-dihydro-2H-pyran obtained under Overman rearrangement conditions
|
Montero, Ana
|
|
2010
|
51 |
2 |
p. 277-280
4 p.
|
artikel
|
| 57 |
Synthesis, crystal structures and photochromic properties of novel chiral Schiff base macrocycles
|
Tanaka, Koichi
|
|
2010
|
51 |
2 |
p. 449-452
4 p.
|
artikel
|
| 58 |
Synthesis of 6-imino-5-tetrahydro-1H-2-pyrrolylidenhexahydro-2,4-pyrimidinediones as intermediates for the synthesis of C-azanucleosides
|
Martirosyan, Ashot
|
|
2010
|
51 |
2 |
p. 231-233
3 p.
|
artikel
|
| 59 |
Synthesis of 3-methoxy-quinoxalin-2-ones from methyl trimethoxyacetate and phenylenediamines
|
Venable, Jennifer D.
|
|
2010
|
51 |
2 |
p. 337-339
3 p.
|
artikel
|
| 60 |
Synthesis of N-amino- and N-nitramino-nitroimidazoles
|
Duddu, Raja
|
|
2010
|
51 |
2 |
p. 399-401
3 p.
|
artikel
|
| 61 |
Synthesis of new thieno[3,2-b]pyridine derivatives by palladium-catalyzed couplings and intramolecular cyclizations
|
Calhelha, Ricardo C.
|
|
2010
|
51 |
2 |
p. 281-283
3 p.
|
artikel
|
| 62 |
The first ‘alkane-like’ functionalization of n-alkyl acetates: a new method for one-pot selective syntheses of bifunctional aliphatic compounds with an acetate group
|
Orlinkov, Alexander V.
|
|
2010
|
51 |
2 |
p. 259-263
5 p.
|
artikel
|
| 63 |
The first example of the cascade assembly of a spirocyclopropane structure: direct transformation of benzylidenemalononitriles and N,N′-dialkylbarbituric acids into substituted 2-aryl-4,6,8-trioxo-5,7-diazaspiro[2.5]octane-1,1-dicarbonitriles
|
Elinson, Michail N.
|
|
2010
|
51 |
2 |
p. 428-431
4 p.
|
artikel
|
| 64 |
The 4-nitrobenzenesulfonyl group as a convenient N-protecting group for iminosugars—synthesis of oligosaccharide inhibitors of heparanase
|
Csíki, Zsuzsánna
|
|
2010
|
51 |
2 |
p. 391-395
5 p.
|
artikel
|
| 65 |
Theoretical study of three predominant tautomers of 2-oxo-6-methylpurine and their two transition state structures
|
Kim, Jong Hwa
|
|
2010
|
51 |
2 |
p. 354-356
3 p.
|
artikel
|
| 66 |
Total synthesis of fuligocandines A and B
|
Pettersson, Birgitta
|
|
2010
|
51 |
2 |
p. 238-239
2 p.
|
artikel
|
| 67 |
Triphenylamine-based receptor for selective recognition of dicarboxylates
|
Ghosh, Kumaresh
|
|
2010
|
51 |
2 |
p. 343-347
5 p.
|
artikel
|
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