| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A chemoenzymatic synthesis of both enantiomers of a cis-lignan lactone
|
Chênevert, Robert
|
|
1998
|
9 |
16 |
p. 2827-2831
5 p.
|
artikel
|
| 2 |
A convenient preparation of taxoid right-half building blocks
|
Arseniyadis, Siméon
|
|
1998
|
9 |
16 |
p. 2871-2878
8 p.
|
artikel
|
| 3 |
An efficient and general enantioselective synthesis of some isoxazole-containing analogues of the neuroexcitant glutamic acid
|
Pajouhesh, Hassan
|
|
1998
|
9 |
16 |
p. 2757-2760
4 p.
|
artikel
|
| 4 |
Asymmetric allenylation of aliphatic aldehydes catalyzed by a chiral formamide
|
Iseki, Katsuhiko
|
|
1998
|
9 |
16 |
p. 2889-2894
6 p.
|
artikel
|
| 5 |
Asymmetric hydrogenation of (E)-α,β-bis(N-acylamino)acrylates catalyzed by a rhodium complex with trans-chelating chiral diphosphine ligand
|
Kuwano, Ryoichi
|
|
1998
|
9 |
16 |
p. 2773-2775
3 p.
|
artikel
|
| 6 |
Asymmetric synthesis of (S)-α-methyl α-amino acids by alkylation of chiral 3,6-dihydro-2H-1,4-oxazin-2-ones using unactivated alkyl halides and organic bases
|
Chinchilla, Rafael
|
|
1998
|
9 |
16 |
p. 2769-2772
4 p.
|
artikel
|
| 7 |
Calculation of the efficiency of purification by crystallization of ideal multicomponent stereoisomeric mixtures
|
Smith, Alan A
|
|
1998
|
9 |
16 |
p. 2925-2937
13 p.
|
artikel
|
| 8 |
Chiral ligands derived from abrine. Part 5: Substituent effects on asymmetric induction in enantioselective addition of diethylzinc to benzaldehyde catalyzed by chiral oxazolidines possessing an indole moiety
|
Zhu, Hua-Jie
|
|
1998
|
9 |
16 |
p. 2879-2888
10 p.
|
artikel
|
| 9 |
Convenient access to both enantiomers of new azido- and aminoinositols via a chemoenzymatic route
|
Sanfilippo, Claudia
|
|
1998
|
9 |
16 |
p. 2809-2817
9 p.
|
artikel
|
| 10 |
Deracemisation of α-amino acids—(R)- and (S)-phenylalanine from the same enantiomer of a homochiral auxiliary
|
Bull, Steven D
|
|
1998
|
9 |
16 |
p. 2795-2798
4 p.
|
artikel
|
| 11 |
Deracemization of compounds possessing a sec-alcohol or -amino group through a cyclic oxidation–reduction sequence: a kinetic treatment
|
Kroutil, Wolfgang
|
|
1998
|
9 |
16 |
p. 2901-2913
13 p.
|
artikel
|
| 12 |
Determination of the absolute configuration of an unexpectedly stable N-silylated isomer isolated en route to the trinem antibiotic GV129606
|
Pecunioso, Angelo
|
|
1998
|
9 |
16 |
p. 2787-2790
4 p.
|
artikel
|
| 13 |
Efficient asymmetric synthesis of ABT-594; a potent, orally effective analgesic
|
Lynch, John K.
|
|
1998
|
9 |
16 |
p. 2791-2794
4 p.
|
artikel
|
| 14 |
Enantioselective formal synthesis of (−)-ovalicin using quinic acid as a chiral template 1 Keywords: natural products; antitumor compounds; stereospecific hydroxylation; oxiranes. 1
|
Barco, Achille
|
|
1998
|
9 |
16 |
p. 2857-2864
8 p.
|
artikel
|
| 15 |
Enzymatic resolution of (RS)-2-arylpropionic acid thioesters by Candida rugosa lipase-catalyzed thiotransesterification or hydrolysis in organic solvents
|
Chang, Chun-Sheng
|
|
1998
|
9 |
16 |
p. 2799-2807
9 p.
|
artikel
|
| 16 |
5-epi-Deoxyrhamnojirimycin is a potent inhibitor of an α-l-rhamnosidase: 5-epi-deoxymannojirimycin is not a potent inhibitor of an α-d-mannosidase
|
Davis, Benjamin G.
|
|
1998
|
9 |
16 |
p. 2947-2960
14 p.
|
artikel
|
| 17 |
Erratum
|
|
|
1998
|
9 |
16 |
p. 2755-
1 p.
|
artikel
|
| 18 |
Intramolecular aminolysis of trichloroethyl esters: a mild macrocyclization protocol for the preparation of cryptophycin derivatives
|
Fray, Andrew H.
|
|
1998
|
9 |
16 |
p. 2777-2781
5 p.
|
artikel
|
| 19 |
Lipase-catalysed chemoselective monoacetylation of hydroxyalkylphenols and chemoselective removal of a single acetyl group from their diacetates
|
Allevi, Pietro
|
|
1998
|
9 |
16 |
p. 2915-2924
10 p.
|
artikel
|
| 20 |
New access to enantiopure O,O′-dibenzoyltartaric acid: resolution of the mixed calcium methoxyacetate by preferential crystallization
|
Elekes, Ferenc
|
|
1998
|
9 |
16 |
p. 2895-2900
6 p.
|
artikel
|
| 21 |
New one pot synthesis of a chiral α-hydroxy-γ-butyrolactone via sequential asymmetric hydrogenation of an α,γ-diketoester
|
Blandin, Véronique
|
|
1998
|
9 |
16 |
p. 2765-2768
4 p.
|
artikel
|
| 22 |
New synthesis of enantiomerically pure (S)-3-amino-2-phenyl propanoic acid via the asymmetric transformation of its racemic N-phthaloyl derivative
|
Calmes, Monique
|
|
1998
|
9 |
16 |
p. 2845-2850
6 p.
|
artikel
|
| 23 |
Organic co-solvents restore the inherently high enantiomeric ratio of lipase B from Candida antarctica in hydrolytic resolution by relieving the enantiospecific inhibition of product alcohol
|
Lundhaug, Kamilla
|
|
1998
|
9 |
16 |
p. 2851-2856
6 p.
|
artikel
|
| 24 |
Photochemical desulfurization of l-cysteine derivatives 1 Dedicated to the memory of Dr. Francesc R. Trull. 1
|
González, Asensio
|
|
1998
|
9 |
16 |
p. 2761-2764
4 p.
|
artikel
|
| 25 |
Practical synthesis of a differentially protected myo-inositol
|
Kornienko, Alexander
|
|
1998
|
9 |
16 |
p. 2783-2786
4 p.
|
artikel
|
| 26 |
Preparation and resolution of 2,2′-dimercapto-6,6′-dimethoxy-1,1′-biphenyl: a C 2-symmetric sulfur building block
|
Delogu, Giovanna
|
|
1998
|
9 |
16 |
p. 2819-2826
8 p.
|
artikel
|
| 27 |
Production of chiral hydroxy long chain fatty acids by whole cell biocatalysis of pentadecanoic acid with an E. coli recombinant containing cytochrome P450BM-3 monooxygenase
|
Schneider, Silke
|
|
1998
|
9 |
16 |
p. 2832-2844
13 p.
|
artikel
|
| 28 |
Resolution of the enantiomers of tetrahydrozoline by chiral HPLC. The racemization of the enantiomers via an imine–enamine tautomerism
|
Caccamese, Salvatore
|
|
1998
|
9 |
16 |
p. 2939-2945
7 p.
|
artikel
|
| 29 |
Single-chiral bis(oxazolinyl)pyridine (pybox). Efficiency in asymmetric catalytic cyclopropanation
|
Nishiyama, Hisao
|
|
1998
|
9 |
16 |
p. 2865-2869
5 p.
|
artikel
|
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