nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A biogenetically inspired heterodimerization approach to the synthesis of the core structure of the alkaloid fissoldhimine
|
Twin, Heather |
|
2007 |
48 |
10 |
p. 1841-1844 4 p. |
artikel |
2 |
An efficient and versatile route to the synthesis of 9,10-dihydro-3-formylphenanthrenes
|
Pratap, Ramendra |
|
2007 |
48 |
10 |
p. 1715-1719 5 p. |
artikel |
3 |
A novel and convenient synthesis of 5-aryl-4-bromo-3-carboxyisoxazoles: useful intermediates for the solid-phase synthesis of 4,5-diarylisoxazoles
|
Letourneau, Jeffrey J. |
|
2007 |
48 |
10 |
p. 1739-1743 5 p. |
artikel |
4 |
An unprecedented methylene oxidation accompanying the aza Diels–Alder reactions of acyclic unactivated alkenes: synthesis of novel quinolin-3-one substituted pyrimidinone derivatives
|
Mohan, Chander |
|
2007 |
48 |
10 |
p. 1711-1713 3 p. |
artikel |
5 |
1,2-Bis(2,5-diphenylphospholano)methane, a new ligand for asymmetric hydrogenation
|
Jackson, Mark |
|
2007 |
48 |
10 |
p. 1831-1834 4 p. |
artikel |
6 |
Calendar
|
|
|
2007 |
48 |
10 |
p. I-III nvt p. |
artikel |
7 |
Carbon–bromine cleavage by dimethyl sulfoxide: the key step of C(5) functionalization of push–pull 2-alkylidene-4-oxothiazolidine vinyl bromides
|
Baranac Stojanović, Marija |
|
2007 |
48 |
10 |
p. 1695-1698 4 p. |
artikel |
8 |
Chiral P,O-ligands derived from N,O-phenylene prolinols for palladium-catalyzed asymmetric allylic alkylation
|
Jiang, Biao |
|
2007 |
48 |
10 |
p. 1703-1706 4 p. |
artikel |
9 |
Copper(I) iodide dimethyl sulfide catalyzed 1,4-addition of alkenyl groups from alkenyl-alkylzincate reagents
|
El-Batta, Amer |
|
2007 |
48 |
10 |
p. 1761-1765 5 p. |
artikel |
10 |
Corrigendum to “Non-linear effects in acyclic amino acid-catalyzed direct asymmetric aldol reactions”
|
Dziedzic, Pawel |
|
2007 |
48 |
10 |
p. 1875- 1 p. |
artikel |
11 |
Dioxadispiroketal compounds and a potential acyclic precursor from Amomum aculeatum
|
Salim, Angela A. |
|
2007 |
48 |
10 |
p. 1849-1853 5 p. |
artikel |
12 |
Eco-friendly synthesis of imines by ultrasound irradiation
|
Guzen, Karla P. |
|
2007 |
48 |
10 |
p. 1845-1848 4 p. |
artikel |
13 |
Editorial board
|
|
|
2007 |
48 |
10 |
p. CO2- 1 p. |
artikel |
14 |
Efficient and rapid synthesis of 1-substituted-1H-1,2,3,4-tetrazoles in the acidic ionic liquid 1-n-butylimidazolium tetrafluoroborate
|
Potewar, Taterao M. |
|
2007 |
48 |
10 |
p. 1721-1724 4 p. |
artikel |
15 |
Enzyme promiscuity: first protein-catalyzed Morita–Baylis–Hillman reaction
|
Reetz, Manfred T. |
|
2007 |
48 |
10 |
p. 1679-1681 3 p. |
artikel |
16 |
Evaluation of polymer-supported vinyltin reagents in the Stille cross-coupling reaction
|
Chrétien, Jean-Mathieu |
|
2007 |
48 |
10 |
p. 1781-1785 5 p. |
artikel |
17 |
First total synthesis of tuberonic acid
|
Nonaka, Hisato |
|
2007 |
48 |
10 |
p. 1745-1748 4 p. |
artikel |
18 |
Glycosylative transcarbamylation: efficient transformation of tert-butyl carbamates to novel glycoconjugates
|
Henry Jr., Kenneth J. |
|
2007 |
48 |
10 |
p. 1791-1794 4 p. |
artikel |
19 |
Graphical contents list
|
|
|
2007 |
48 |
10 |
p. 1667-1678 12 p. |
artikel |
20 |
Hg(OTf)2-Catalyzed cycloisomerization of 2-ethynylaniline derivatives leading to indoles
|
Kurisaki, Takahiro |
|
2007 |
48 |
10 |
p. 1871-1874 4 p. |
artikel |
21 |
Highly efficient and regioselective synthesis of keto-enamine Schiff bases of 7-hydroxy-4-methyl-2-oxo-2H-benzo[h]chromene-8,10-dicarbaldehyde and 1-hydroxynaphthalene-2,4-dicarbaldehyde
|
Sashidhara, Koneni V. |
|
2007 |
48 |
10 |
p. 1699-1702 4 p. |
artikel |
22 |
(IBC) Guide to Authors (2006)
|
|
|
2007 |
48 |
10 |
p. CO3- 1 p. |
artikel |
23 |
Mercury extraction by ionic liquids: temperature and alkyl chain length effect
|
Germani, Raimondo |
|
2007 |
48 |
10 |
p. 1767-1769 3 p. |
artikel |
24 |
Methylrhenium oxides
|
Rost, Alexandra M.J. |
|
2007 |
48 |
10 |
p. 1775-1779 5 p. |
artikel |
25 |
Mild, efficient and selective hydrolysis of polymer-supported methyl esters using trimethyltin hydroxide
|
Méndez, Luciana |
|
2007 |
48 |
10 |
p. 1757-1760 4 p. |
artikel |
26 |
Molecular modeling study for a novel structured oligomer subunit selection: the example of 2-aminomethyl-phenyl-acetic acid
|
Raynal, Nicolas |
|
2007 |
48 |
10 |
p. 1787-1790 4 p. |
artikel |
27 |
N,N′,N″-Tri-Boc-guanidine (TBG): a common starting material for both N-alkyl guanidines and amidinoureas
|
Prabhakaran, Panchami |
|
2007 |
48 |
10 |
p. 1725-1727 3 p. |
artikel |
28 |
Novel chiral solvating agents derived from natural amino acid: enantiodiscrimination for chiral α-arylalkylamines
|
Luo, Zengwei |
|
2007 |
48 |
10 |
p. 1753-1756 4 p. |
artikel |
29 |
Novel Mg2+-responsive fluorescent chemosensor based on benzo-15-crown-5 possessing 1-naphthaleneacetamide moiety
|
Hama, Hiroya |
|
2007 |
48 |
10 |
p. 1859-1861 3 p. |
artikel |
30 |
One-pot synthesis of polysubstituted indoles from aliphatic nitro compounds under mild conditions
|
Simoneau, Christopher A. |
|
2007 |
48 |
10 |
p. 1809-1811 3 p. |
artikel |
31 |
Oxidative-substitution reactions of electron-rich aromatic compounds with BF3-activated iodonium ylides
|
Telu, Sanjay |
|
2007 |
48 |
10 |
p. 1863-1866 4 p. |
artikel |
32 |
Products of the addition of 1,4-naphthoquinone to an acecyclone
|
Bubenik, Monica P. |
|
2007 |
48 |
10 |
p. 1801-1803 3 p. |
artikel |
33 |
Ring opening of 2-(cyanomethyl)aziridines by acid chlorides: synthesis of novel 4-amino-2-butenenitrile derivatives through intermediate aziridinium salts
|
D’hooghe, Matthias |
|
2007 |
48 |
10 |
p. 1771-1774 4 p. |
artikel |
34 |
Solvent-free microwave-assisted conversion of Baylis–Hillman adducts of ninhydrin into functionalized spiropyrrolidines/pyrrolizidines through 1,3-dipolar cycloaddition
|
Ramesh, Ekambaram |
|
2007 |
48 |
10 |
p. 1835-1839 5 p. |
artikel |
35 |
Stereoselective intramolecular 1,3-dipolar nitrile oxide cycloaddition reaction of N-formyl-β-nitroamides
|
Kadowaki, Ayako |
|
2007 |
48 |
10 |
p. 1823-1825 3 p. |
artikel |
36 |
Stereoselective synthesis of belactosin C and its derivatives using a catalytic proline catalyzed crossed-aldol reaction
|
Kumaraswamy, G. |
|
2007 |
48 |
10 |
p. 1707-1709 3 p. |
artikel |
37 |
Stilbene-bridged 1,3-alternate calix[4]arene crown ether for selective alkali ion extraction
|
Jaiyu, Arisa |
|
2007 |
48 |
10 |
p. 1817-1821 5 p. |
artikel |
38 |
Studies of ring-closing mode of 4-hydroxy-2-vinylidenebutanoates: 5-exo-trig versus 5-endo-dig
|
Kitagaki, Shinji |
|
2007 |
48 |
10 |
p. 1735-1738 4 p. |
artikel |
39 |
Synthesis of chlorinated β- and γ-lactones from unsaturated acids with sodium hypochlorite and Lewis acids
|
López-López, José A. |
|
2007 |
48 |
10 |
p. 1749-1752 4 p. |
artikel |
40 |
The application of non-cross-linked polystyrene-supported triphenylarsine in Stille coupling reactions
|
Lau, Kelvin Chi Yin |
|
2007 |
48 |
10 |
p. 1813-1816 4 p. |
artikel |
41 |
The diastereoselective synthesis of functionalised spirocyclic lactams and lactones using a Cope elimination/intramolecular nitrone cycloaddition strategy
|
Ellis, Gemma L. |
|
2007 |
48 |
10 |
p. 1687-1690 4 p. |
artikel |
42 |
The first example of 2,2-dilithiocyanocyclopropanes: generation from 2-bromo-2-sulfinylcyanocyclopropanes with tert-butyllithium, property, and a synthesis of fully substituted cyanocyclopropanes
|
Fukushima, Iori |
|
2007 |
48 |
10 |
p. 1855-1858 4 p. |
artikel |
43 |
The synthesis of functionalised chiral bicyclic lactam and lactone N-oxides using a tandem Cope elimination/reverse Cope elimination protocol
|
Ellis, Gemma L. |
|
2007 |
48 |
10 |
p. 1683-1686 4 p. |
artikel |
44 |
The synthesis of highly functionalized morpholine N-oxides from ephedrine and pseudoephedrine utilizing a tandem Cope elimination/reverse Cope elimination protocol
|
Henry, Neil |
|
2007 |
48 |
10 |
p. 1691-1694 4 p. |
artikel |
45 |
Total synthesis of (±)-debromoflustramine B and E and (±)-debromoflustramide B based on one-pot intramolecular Ullmann coupling and Claisen rearrangement
|
Miyamoto, Hiroshi |
|
2007 |
48 |
10 |
p. 1805-1808 4 p. |
artikel |
46 |
Towards the total chemical synthesis of integral membrane proteins: a general method for the synthesis of hydrophobic peptide-αthioester building blocks
|
Johnson, Erik C.B. |
|
2007 |
48 |
10 |
p. 1795-1799 5 p. |
artikel |
47 |
Toward the total synthesis of Scleritodermin A: preparation of the C1–N15 fragment
|
Sellanes, Diver |
|
2007 |
48 |
10 |
p. 1827-1830 4 p. |
artikel |
48 |
Unmasking of aminoanthroquinone moiety through a ring opening in the presence of copper salts and a subsequent cross-coupling/recyclization cascade
|
Vasilevsky, S.F. |
|
2007 |
48 |
10 |
p. 1867-1870 4 p. |
artikel |
49 |
Zinc oxide as an economical and efficient catalyst for the one-pot preparation of β-acetamido ketones via a four-component condensation reaction
|
Maghsoodlou, Malek Taher |
|
2007 |
48 |
10 |
p. 1729-1734 6 p. |
artikel |