| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A facile one-pot conversion of non-enolizable aldehydes to diazirines
|
Likhotvorik, Igor R
|
|
2000
|
41 |
6 |
p. 795-796
2 p.
|
artikel
|
| 2 |
A modified procedure for the deprotection of methoxymethyl ether
|
Yu, Chengzhi
|
|
2000
|
41 |
6 |
p. 819-822
4 p.
|
artikel
|
| 3 |
An enantioselective synthesis of (1S,2S)-pseudoephedrine † IICT Communication No. 4346. †
|
Reddy, G.Vidyasagar
|
|
2000
|
41 |
6 |
p. 953-954
2 p.
|
artikel
|
| 4 |
A practical protocol for chemoselective N-methylation of vicinal amino alcohols
|
Reddy, G.Vidyasagar
|
|
2000
|
41 |
6 |
p. 949-951
3 p.
|
artikel
|
| 5 |
A rapid entry into major groups of taxoids
|
Ignacio Martı́n Hernando, José
|
|
2000
|
41 |
6 |
p. 863-866
4 p.
|
artikel
|
| 6 |
Asymmetric catalytic Pauson–Khand reactions with chiral phosphine ligands: Dramatic effects of substituents in 1,6-enyne systems
|
Hiroi, Kunio
|
|
2000
|
41 |
6 |
p. 891-895
5 p.
|
artikel
|
| 7 |
Asymmetric Strecker reactions of ketimines catalysed by titanium-based complexes
|
Byrne, Janice J
|
|
2000
|
41 |
6 |
p. 873-876
4 p.
|
artikel
|
| 8 |
A very short route to the functionalized A-ring moiety of ciguatoxin
|
Oguri, Hiroki
|
|
2000
|
41 |
6 |
p. 975-978
4 p.
|
artikel
|
| 9 |
Barbier-type reactions of nitriles and alkyl iodides mediated by samarium(II) iodide in the presence of catalytic nickel(II) iodide
|
Kang, Han-Young
|
|
2000
|
41 |
6 |
p. 937-939
3 p.
|
artikel
|
| 10 |
Biogenetically patterned synthesis of camptothecin and 20-deoxycamptothecin
|
Brown, Richard T
|
|
2000
|
41 |
6 |
p. 859-862
4 p.
|
artikel
|
| 11 |
α-Chloroacetyl capping of peptides: an N-terminal capping strategy suitable for Edman sequencing
|
Shogren-Knaak, Michael A
|
|
2000
|
41 |
6 |
p. 827-829
3 p.
|
artikel
|
| 12 |
[2+2] Cycloaddition reactions of imines with alkynyl selenides catalyzed by scandium triflate
|
Ma, Yun
|
|
2000
|
41 |
6 |
p. 945-947
3 p.
|
artikel
|
| 13 |
Dehydrogenative silylation of terminal alkynes by iridium catalyst
|
Shimizu, Rie
|
|
2000
|
41 |
6 |
p. 907-910
4 p.
|
artikel
|
| 14 |
Efficient convergent synthesis of a trans-fused 6-6-6-6-membered tetracyclic ether ring system
|
Matsuo, Goh
|
|
2000
|
41 |
6 |
p. 903-906
4 p.
|
artikel
|
| 15 |
Erratum
|
|
|
2000
|
41 |
6 |
p. 987-
1 p.
|
artikel
|
| 16 |
Geminal hydroxy phosphonate derivatives of nucleosides: A novel class of nucleoside 5′-monophosphate analogues
|
Králı́ková, Šárka
|
|
2000
|
41 |
6 |
p. 955-958
4 p.
|
artikel
|
| 17 |
HFC-134a as a fluorinated building block: short syntheses of α-fluoroenones
|
Bainbridge, J.Marie
|
|
2000
|
41 |
6 |
p. 971-974
4 p.
|
artikel
|
| 18 |
Hydrogenation of alkenes or alkynes using decaborane in methanol
|
Lee, Seung Hwan
|
|
2000
|
41 |
6 |
p. 887-889
3 p.
|
artikel
|
| 19 |
Mitsunobu reaction modifications allowing product isolation without chromatography: application to a small parallel library
|
Pelletier, Jeffrey C.
|
|
2000
|
41 |
6 |
p. 797-800
4 p.
|
artikel
|
| 20 |
Nickel(0)-catalyzed coupling of vinylzirconiums to α-bromo-α,α-difluoro esters. Convenient generation of a functionalized allyldifluoro moiety
|
Schwaebe, Michael K
|
|
2000
|
41 |
6 |
p. 791-794
4 p.
|
artikel
|
| 21 |
Novel carbohydrate scaffolds. Assembly of a uridine–mannose scaffold based on tunicamycin
|
Silva, Domingos J
|
|
2000
|
41 |
6 |
p. 855-858
4 p.
|
artikel
|
| 22 |
Novel 17α-ethynylestradiol derivatives: Sonogashira couplings using unprotected phenylhydrazines
|
Arterburn, Jeffrey B
|
|
2000
|
41 |
6 |
p. 839-842
4 p.
|
artikel
|
| 23 |
One-pot selective synthesis of β-nitrostyrenes from styrenes, promoted by Cu(II)
|
Campos, Pedro J
|
|
2000
|
41 |
6 |
p. 979-982
4 p.
|
artikel
|
| 24 |
Palladium-catalyzed functionalization of 5- and 7-azaindoles
|
Chi, Sung Min
|
|
2000
|
41 |
6 |
p. 919-922
4 p.
|
artikel
|
| 25 |
Practical unequivocal synthesis of phosphatidyl-myo-inositols
|
Aneja, Rajindra
|
|
2000
|
41 |
6 |
p. 847-850
4 p.
|
artikel
|
| 26 |
Regiospecific synthesis of 2A,2B-disulfonated γ-cyclodextrin
|
Teranishi, Katsunori
|
|
2000
|
41 |
6 |
p. 933-936
4 p.
|
artikel
|
| 27 |
Remote chiral induction in the thio-Claisen rearrangement of bicyclic thiolactams
|
Watson, Daniel J
|
|
2000
|
41 |
6 |
p. 815-818
4 p.
|
artikel
|
| 28 |
Solid phase chemistry at a modified cathode surface. First synthesis of a polyamine precursor
|
Marchand, Gilles
|
|
2000
|
41 |
6 |
p. 883-885
3 p.
|
artikel
|
| 29 |
Solid phase sequential 1,3-dipolar cycloaddition–Pictet–Spengler reactions
|
Dondas, H.Ali
|
|
2000
|
41 |
6 |
p. 967-970
4 p.
|
artikel
|
| 30 |
Solid phase synthesis of 1-substituted pyroglutamates
|
Alvarez-Gutierrez, Julia M
|
|
2000
|
41 |
6 |
p. 851-854
4 p.
|
artikel
|
| 31 |
Stereoselective synthesis of 5-monoalkyl and 5,5-dialkylsubstituted noviose derivatives
|
Periers, Anne-Marie
|
|
2000
|
41 |
6 |
p. 867-871
5 p.
|
artikel
|
| 32 |
Study into the cyclization of an epoxy-alcohol to the energetically disfavored product by peptides from non-biased combinatorial libraries
|
Chiosis, Gabriela
|
|
2000
|
41 |
6 |
p. 801-806
6 p.
|
artikel
|
| 33 |
Synthesis and characterisation of poly (l-lactic acid) galactosyl derivatives; access to functionalised microspheres
|
Kassab, Rima
|
|
2000
|
41 |
6 |
p. 877-881
5 p.
|
artikel
|
| 34 |
Synthesis of a complete set of l-difluorophenylalanines, l-(F2)Phe, as molecular explorers for the CH/π interaction between peptide ligand and receptor
|
Fujita, Tsugumi
|
|
2000
|
41 |
6 |
p. 923-927
5 p.
|
artikel
|
| 35 |
Synthesis of aryl α-keto-acids via the Cu-catalyzed conversion of aryl nitroaldol products
|
Nikalje, Milind D
|
|
2000
|
41 |
6 |
p. 959-961
3 p.
|
artikel
|
| 36 |
Synthesis of marine sesterterpenoid dysidiolide
|
Miyaoka, Hiroaki
|
|
2000
|
41 |
6 |
p. 911-914
4 p.
|
artikel
|
| 37 |
Synthesis of novel spirolactams by reaction of fluorescein methyl ester with amines
|
Adamczyk, Maciej
|
|
2000
|
41 |
6 |
p. 807-809
3 p.
|
artikel
|
| 38 |
Synthesis of SB 222618. A potential PDE IV inhibitor † This work is dedicated to the memory of Dr. Lendon Pridgen †
|
Conde, Jose J
|
|
2000
|
41 |
6 |
p. 811-814
4 p.
|
artikel
|
| 39 |
Synthesis of the 4-arylindole portion of the antitumor agent diazonamide and related studies
|
Chan, Fiona
|
|
2000
|
41 |
6 |
p. 835-838
4 p.
|
artikel
|
| 40 |
Synthesis of the dichlorobisoxazole-indole portion of the antitumor agent diazonamide by a putative biogenetic strategy
|
Magnus, Philip
|
|
2000
|
41 |
6 |
p. 831-834
4 p.
|
artikel
|
| 41 |
Synthesis, structure, and redox properties of a quinone-bridged calix[6]arene
|
Akine, Shigehisa
|
|
2000
|
41 |
6 |
p. 897-901
5 p.
|
artikel
|
| 42 |
Synthetic studies towards phorboxazole A. Stereoselective synthesis of the C3–C19 bis-oxane oxazole portion of the phorboxazole macrolide
|
Pattenden, Gerald
|
|
2000
|
41 |
6 |
p. 983-986
4 p.
|
artikel
|
| 43 |
The efficient entry into the tricyclic core of halichlorine
|
Shindo, Mitsuru
|
|
2000
|
41 |
6 |
p. 929-932
4 p.
|
artikel
|
| 44 |
The reaction of amines with an electrogenerated base. Improved synthesis of arylcarbamic esters
|
Feroci, Marta
|
|
2000
|
41 |
6 |
p. 963-966
4 p.
|
artikel
|
| 45 |
The synthesis of enantiomerically pure disubstituted aziridines and N -alkoxy aziridines
|
Hanessian, Stephen
|
|
2000
|
41 |
6 |
p. 787-790
4 p.
|
artikel
|
| 46 |
Total synthesis of 15-deoxoclerocidin
|
Kende, A.S
|
|
2000
|
41 |
6 |
p. 843-846
4 p.
|
artikel
|
| 47 |
Total synthesis of (±)-desoxycodeine-d: a novel route to the morphine skeleton
|
Liou, Jing-Ping
|
|
2000
|
41 |
6 |
p. 915-918
4 p.
|
artikel
|
| 48 |
Total synthesis of 6-epi-sarsolilide A
|
Zhang, Jiazhong
|
|
2000
|
41 |
6 |
p. 941-943
3 p.
|
artikel
|
| 49 |
Total synthesis of lipoxin A4 and lipoxin B4 from butadiene
|
Rodrı́guez, A
|
|
2000
|
41 |
6 |
p. 823-826
4 p.
|
artikel
|
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