| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A chemoselective aniline–chloropyrimidine coupling in a competing electrophilic environment
|
Choudhury, Anusuya
|
|
2008
|
49 |
1 |
p. 102-105
4 p.
|
artikel
|
| 2 |
An efficient synthesis of fluorocyclopentenes using fluoroalkylidenecarbenes
|
Guan, Tong
|
|
2008
|
49 |
1 |
p. 76-79
4 p.
|
artikel
|
| 3 |
A new photolabile carboxyl protecting group for native chemical ligation
|
Briand, Benoît
|
|
2008
|
49 |
1 |
p. 85-87
3 p.
|
artikel
|
| 4 |
Application of microwave method to the solid phase synthesis of pseudopeptides containing ester bond
|
Joshi, Bishnu Prasad
|
|
2008
|
49 |
1 |
p. 98-101
4 p.
|
artikel
|
| 5 |
Au(I)-catalyzed efficient synthesis of α-acyloxy-α′-silyl ketones from α-acyloxy-α-alkynylsilanes
|
Sakaguchi, Kazuhiko
|
|
2008
|
49 |
1 |
p. 25-28
4 p.
|
artikel
|
| 6 |
2,6-Bis(2-benzimidazolyl)pyridine as a chemosensor for fluoride ions
|
Chetia, Bolin
|
|
2008
|
49 |
1 |
p. 94-97
4 p.
|
artikel
|
| 7 |
Boric acid: an efficient and environmentally benign catalyst for transesterification of ethyl acetoacetate
|
Kondaiah, G.C.M.
|
|
2008
|
49 |
1 |
p. 106-109
4 p.
|
artikel
|
| 8 |
Calendar
|
|
|
2008
|
49 |
1 |
p. I-II
nvt p.
|
artikel
|
| 9 |
Catalytic synthesis of 1,4-dihydropyridine derivatives using scandium(III) triflate
|
Kikuchi, Satoshi
|
|
2008
|
49 |
1 |
p. 114-116
3 p.
|
artikel
|
| 10 |
Copper-catalyzed synthesis of primary arylamines from aryl halides and 2,2,2-trifluoroacetamide
|
Tao, Chuan-Zhou
|
|
2008
|
49 |
1 |
p. 70-75
6 p.
|
artikel
|
| 11 |
Cyclisation reactions of bis-protected guanidines
|
Albrecht, Christiane
|
|
2008
|
49 |
1 |
p. 185-188
4 p.
|
artikel
|
| 12 |
Desulfurization of sultams with simultaneous methylenation
|
Rogachev, Victor O.
|
|
2008
|
49 |
1 |
p. 133-136
4 p.
|
artikel
|
| 13 |
Dynamic kinetic resolution of hemiaminals using a novel DMAP catalyst
|
Yamada, Shinji
|
|
2008
|
49 |
1 |
p. 32-35
4 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2008
|
49 |
1 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Efficient access to 5-substituted thiazoles by a novel metallotropic rearrangement
|
Zambon, Alfonso
|
|
2008
|
49 |
1 |
p. 66-69
4 p.
|
artikel
|
| 16 |
Efficient organocatalysis with a calix[4]pyrrole derivative
|
Cafeo, Grazia
|
|
2008
|
49 |
1 |
p. 153-155
3 p.
|
artikel
|
| 17 |
Efficient oxidation of alcohols electrochemically mediated by azabicyclo-N-oxyls
|
Demizu, Yosuke
|
|
2008
|
49 |
1 |
p. 48-52
5 p.
|
artikel
|
| 18 |
6-endo-dig Cyclization of heteroarylesters to alkynes promoted by Lewis acid catalyst in the presence of Brønsted acid
|
Hellal, Malik
|
|
2008
|
49 |
1 |
p. 62-65
4 p.
|
artikel
|
| 19 |
Fe3+-Catalyzed transacetalization of 2-alkoxytetrahydrofurans with alcohols
|
Yamanaka, Daisetsu
|
|
2008
|
49 |
1 |
p. 53-56
4 p.
|
artikel
|
| 20 |
FeCl3-catalyzed alkylation of indoles with 1,3-dicarbonyl compounds: an expedient synthesis of 3-substituted indoles
|
Yadav, J.S.
|
|
2008
|
49 |
1 |
p. 199-202
4 p.
|
artikel
|
| 21 |
First isolation of 1,2-dithietan-3-one from α-dithiolactone
|
Shigetomi, Toshiyuki
|
|
2008
|
49 |
1 |
p. 36-38
3 p.
|
artikel
|
| 22 |
Graphical contents list
|
|
|
2008
|
49 |
1 |
p. 1-12
12 p.
|
artikel
|
| 23 |
Guide for Authors (2006)
|
|
|
2008
|
49 |
1 |
p. III-VI
nvt p.
|
artikel
|
| 24 |
Highly efficient catalytic system for hydrosilylation of ketones with iron(II) acetate–thiophenecarboxylate
|
Furuta, Akihiro
|
|
2008
|
49 |
1 |
p. 110-113
4 p.
|
artikel
|
| 25 |
Highly regioselective propanoylation of dihydroxybenzenes mediated by Candida antarctica lipase B in organic solvents
|
Miyazawa, Toshifumi
|
|
2008
|
49 |
1 |
p. 175-178
4 p.
|
artikel
|
| 26 |
Highly selective imine-linked fluorescent chemosensor for adenine employing multiple hydrogen bonding
|
Singh, Narinder
|
|
2008
|
49 |
1 |
p. 44-47
4 p.
|
artikel
|
| 27 |
Iodine-catalyzed allylation of 1,3-dicarbonyl compounds with allylic alcohols at room temperature
|
Rao, Weidong
|
|
2008
|
49 |
1 |
p. 122-126
5 p.
|
artikel
|
| 28 |
Lewis acid-catalyzed Prins-type reactions of methylenecyclopropylcarbinols with aldehydes and aldimines
|
Shao, Li-Xiong
|
|
2008
|
49 |
1 |
p. 165-168
4 p.
|
artikel
|
| 29 |
Modified o-methyl-substituted IBX: room temperature oxidation of alcohols and sulfides in common organic solvents
|
Moorthy, Jarugu Narasimha
|
|
2008
|
49 |
1 |
p. 80-84
5 p.
|
artikel
|
| 30 |
Observation of differential reactivity of cyclic amines in SN2 and SNAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors
|
Hopper, Darrin W.
|
|
2008
|
49 |
1 |
p. 137-140
4 p.
|
artikel
|
| 31 |
Ozonolysis of Morita–Baylis–Hillman adducts originated from aromatic aldehydes: an expeditious diastereoselective approach for the preparation of α,β-dihydroxy-esters
|
Abella, Carlos A.M.
|
|
2008
|
49 |
1 |
p. 145-148
4 p.
|
artikel
|
| 32 |
Polymorphism-dependent fluorescence of 9,10-bis(pentafluorobenzoyloxy)anthracene
|
Kohmoto, Shigeo
|
|
2008
|
49 |
1 |
p. 39-43
5 p.
|
artikel
|
| 33 |
Practical synthesis of the calcimimetic agent, cinacalcet
|
Thiel, Oliver R.
|
|
2008
|
49 |
1 |
p. 13-15
3 p.
|
artikel
|
| 34 |
Rearrangement of furo[2,3-c]quinoline-2,4(3aH,5H)-diones to furo[3,4-c]quinoline-3,4(1H,5H)-diones
|
Kafka, Stanislav
|
|
2008
|
49 |
1 |
p. 90-93
4 p.
|
artikel
|
| 35 |
Regioselective, photochemical bromination of aromatic compounds using N-bromosuccinimide
|
Chhattise, Prakash K.
|
|
2008
|
49 |
1 |
p. 189-194
6 p.
|
artikel
|
| 36 |
Rhodium(II) catalysed three-component coupling: a novel reaction of in situ generated iodonium ylides
|
Bonge, Hanne Therese
|
|
2008
|
49 |
1 |
p. 57-61
5 p.
|
artikel
|
| 37 |
Schiff’s base phenol–hydrazone derivatives as colorimetric chemosensors for fluoride ions
|
Saravanakumar, Duraisamy
|
|
2008
|
49 |
1 |
p. 127-132
6 p.
|
artikel
|
| 38 |
Solid phase synthesis of N-aminodipeptides in high optical purity
|
Felten, Anne-Sophie
|
|
2008
|
49 |
1 |
p. 156-158
3 p.
|
artikel
|
| 39 |
Stereocalpin A, a bioactive cyclic depsipeptide from the Antarctic lichen Stereocaulon alpinum
|
Seo, Changon
|
|
2008
|
49 |
1 |
p. 29-31
3 p.
|
artikel
|
| 40 |
Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to α-amino aldehydes
|
Cella, Rodrigo
|
|
2008
|
49 |
1 |
p. 16-19
4 p.
|
artikel
|
| 41 |
Sterically encumbered hexakis(alkylseleno)benzenes: conformational behavior of hexakis(iso-propylselenomethyl)benzene toward Hg2+ ions on selective recognition
|
Singh, Jai Deo
|
|
2008
|
49 |
1 |
p. 117-121
5 p.
|
artikel
|
| 42 |
Studies on isocyanides: synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation/intramolecular amidation
|
Marcos, Carlos F.
|
|
2008
|
49 |
1 |
p. 149-152
4 p.
|
artikel
|
| 43 |
Synthesis and characterization of polar functional group substituted mono- and bis-(o-carboranyl)-1,3,5-triazine derivatives
|
Lee, Chai-Ho
|
|
2008
|
49 |
1 |
p. 159-164
6 p.
|
artikel
|
| 44 |
Synthesis of a versatile metacyclophane macrolactam
|
Wang, Mingwen
|
|
2008
|
49 |
1 |
p. 141-144
4 p.
|
artikel
|
| 45 |
Synthesis of the naringinase inhibitors l-swainsonine and related 6-C-methyl-l-swainsonine analogues: (6R)-C-methyl-l-swainsonine is a more potent inhibitor of l-rhamnosidase by an order of magnitude than l-swainsonine
|
Håkansson, Anders E.
|
|
2008
|
49 |
1 |
p. 179-184
6 p.
|
artikel
|
| 46 |
Synthetic study of (−)-lasubine II via sequential cyclization process
|
Lim, Jaebum
|
|
2008
|
49 |
1 |
p. 88-89
2 p.
|
artikel
|
| 47 |
The effect of an N-substituent on the recyclization of (2-aminoaryl)bis(5-tert-butyl-2-furyl)methanes: synthesis of 3-furylindoles and triketoindoles
|
Butin, Alexander V.
|
|
2008
|
49 |
1 |
p. 20-24
5 p.
|
artikel
|
| 48 |
The first example of direct cyclopropylation of arylamines at the 2-position with magnesium cyclopropylidenes
|
Yamada, Yukie
|
|
2008
|
49 |
1 |
p. 169-174
6 p.
|
artikel
|
| 49 |
Watching microwave-promoted chemistry: reaction monitoring using a digital camera interfaced with a scientific microwave apparatus
|
Bowman, Matthew D.
|
|
2008
|
49 |
1 |
p. 195-198
4 p.
|
artikel
|
Tijdschrift beschrijving