nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acid-catalysed hydrolysis of adenosine 5′-phosphorodithiomorpholidate
|
Reese, Colin B. |
|
1994 |
35 |
28 |
p. 5085-5088 4 p. |
artikel |
2 |
A concise route to biaryls : Formal synthesis of biaryl diamino diacid (AB segment) of vancomycin
|
Rama Rao, A.V. |
|
1994 |
35 |
28 |
p. 5039-5042 4 p. |
artikel |
3 |
Acyloin rearrangement of α-hydroxy acetals: Application to the methyl l-mycaroside synthesis
|
Sato, Tadashi |
|
1994 |
35 |
28 |
p. 5027-5030 4 p. |
artikel |
4 |
Alkoxy radicals in organic synthesis. A novel approach to a key intermediate in milbemycin chemistry
|
Hussain, Nigel |
|
1994 |
35 |
28 |
p. 5069-5072 4 p. |
artikel |
5 |
An efficient method for the oxidation of sulfides to sulfones
|
Su, Weiguo |
|
1994 |
35 |
28 |
p. 4955-4958 4 p. |
artikel |
6 |
An expeditious approach for the synthesis of β-hydroxy aryl α-amino acids present in vancomycin
|
Rama Rao, AV |
|
1994 |
35 |
28 |
p. 5043-5046 4 p. |
artikel |
7 |
An improved method of oxazolidinone hydrolysis in the asymmetric synthesis of α-alkylprolines
|
Genin, Michael J. |
|
1994 |
35 |
28 |
p. 4967-4968 2 p. |
artikel |
8 |
A novel general method for 2-aminoglycal synthesis
|
Iglesia-Guerra, Fernando |
|
1994 |
35 |
28 |
p. 5031-5034 4 p. |
artikel |
9 |
A stereochemically general synthesis of methyl 2,4,6-trideoxy-4-methylthio-α-D-ribo-pyranoside, the thio sugar of esperamicin A1
|
Roush, William R. |
|
1994 |
35 |
28 |
p. 4931-4934 4 p. |
artikel |
10 |
Asymmetric synthesis of the hydroxylamino sugar of calicheamicin
|
Roush, William R. |
|
1994 |
35 |
28 |
p. 4935-4938 4 p. |
artikel |
11 |
Biosynthesis of lactacystin. Origin of the carbons and stereospecific NMR assignment of the two diastereotopic methyl groups
|
Nakagawa, Akira |
|
1994 |
35 |
28 |
p. 5009-5012 4 p. |
artikel |
12 |
Biosynthetic studies of eudistomin H in the tunicate Eudistoma olivaceum
|
Shen, Guo Q. |
|
1994 |
35 |
28 |
p. 4923-4926 4 p. |
artikel |
13 |
Catalytic asymmetric synthesis of β-fluoroalkyl-β-amino acids via biomimetic [1,3]-proton shift reaction
|
Soloshonok, Vadim A. |
|
1994 |
35 |
28 |
p. 5063-5064 2 p. |
artikel |
14 |
Competitive nucleophilic aromatic substitution and palladium-catalyzed alkoxycarbonylation of (substituted chloroarene)Cr(CO)3 complexes
|
Carpentier, Jean-François |
|
1994 |
35 |
28 |
p. 4995-4998 4 p. |
artikel |
15 |
Cyclialkylations of conjugated dienones with furans
|
Majetich, George |
|
1994 |
35 |
28 |
p. 4887-4890 4 p. |
artikel |
16 |
Donor-substituted furans and 1,2-bis(trifluoromethyl)ethylene-1,2-dicarbonitrile: A novel rearrangement and its steric course
|
Urrutia-Desmaison, Gonzalo |
|
1994 |
35 |
28 |
p. 4977-4980 4 p. |
artikel |
17 |
Donor-substituted furans and 1,2-bis(trifluoromethyl)ethylene-1,2-dicarbonitrile: The hidden cycloadditions
|
Huisgen, Rolf |
|
1994 |
35 |
28 |
p. 4981-4984 4 p. |
artikel |
18 |
Efficient rhodium-catalyzed hydrogenation of aldehydes and ketones
|
Burk, Mark J. |
|
1994 |
35 |
28 |
p. 4963-4966 4 p. |
artikel |
19 |
Electrochemical reduction of taxoids: Selective preparation of 9-dihydro-, 10-deoxy- and 10-deacetoxy-taxoids
|
Pulicani, Jean-Pierre |
|
1994 |
35 |
28 |
p. 4999-5002 4 p. |
artikel |
20 |
Enantioselective [2,3]Wittig rearrangement involving a chiral boron enolate terminus
|
Fujimoto, Katsuhiko |
|
1994 |
35 |
28 |
p. 5019-5022 4 p. |
artikel |
21 |
Etherification of hydroxysteroids via triflates
|
Belostotskii, Anatoly M. |
|
1994 |
35 |
28 |
p. 5075-5076 2 p. |
artikel |
22 |
Fe(III)-EDTA mediated autoxidation of 2,6-Di-t-butylphenol and substituted hydroquinones by molecular oxygen
|
Sain, Bir |
|
1994 |
35 |
28 |
p. 5083-5084 2 p. |
artikel |
23 |
Generation of octamethylcuneane and octamethylcubane from syn-octamethyltricyclo[4.2.0.02,5]octa-3,7-diene
|
Gleiter, Rolf |
|
1994 |
35 |
28 |
p. 4969-4972 4 p. |
artikel |
24 |
Graphical abstracts
|
|
|
1994 |
35 |
28 |
p. 4873-4886 14 p. |
artikel |
25 |
Guest selectivity of 1,1,2,2-Tetrakis(4-hydroxyphenyl)ethane
|
Suzuki, Hiroshi |
|
1994 |
35 |
28 |
p. 5015-5018 4 p. |
artikel |
26 |
Halichomycin, a new class of potent cytotoxic macrolide produced by an actinomycete from a marine fish
|
Takahashi, Chika |
|
1994 |
35 |
28 |
p. 5013-5014 2 p. |
artikel |
27 |
Hydrolysis of 2′-deoxypurine nucleosides. The effect of substitution at the C-8 position
|
Laayoun, Ali |
|
1994 |
35 |
28 |
p. 4989-4990 2 p. |
artikel |
28 |
Hydrolysis of oligonucleotides containing 8-substituted purine nucleosides. A new route for preparing abasic oligodeoxynucleotides
|
Laayoun, Ali |
|
1994 |
35 |
28 |
p. 4991-4994 4 p. |
artikel |
29 |
Metabolite structure elucidation using NMR micro-/nano-detection
|
Shockcor, John P. |
|
1994 |
35 |
28 |
p. 4919-4922 4 p. |
artikel |
30 |
Michael-type addition of phthalimide salts to chiral α,β-unsaturated imides
|
Cardillo, Giuliana |
|
1994 |
35 |
28 |
p. 5051-5054 4 p. |
artikel |
31 |
N-acyl aziridines - C-acylating agents for the preparation of polyketides
|
Lygo, Barry |
|
1994 |
35 |
28 |
p. 5073-5074 2 p. |
artikel |
32 |
Novel reactivity of stabilized methylenetributylphosphorane: A new mitsunobu reagent
|
Tsunoda, Tetsuto |
|
1994 |
35 |
28 |
p. 5081-5082 2 p. |
artikel |
33 |
Nucleophilic ring opening of tetrahydro-1,3-oxazines and 1,3-oxazolidines by alkynyl anions: A novel synthesis of β-aminoacetylenes
|
Wu, Ming-Jung |
|
1994 |
35 |
28 |
p. 5003-5004 2 p. |
artikel |
34 |
One-step conversion of esters to acyl azides using diethylaluminum azide
|
Rawal, Viresh H. |
|
1994 |
35 |
28 |
p. 4947-4950 4 p. |
artikel |
35 |
On the utility of α-heteroatom substituted orthoesters in the Johnson Claisen rearrangement
|
Elworthy, Todd R. |
|
1994 |
35 |
28 |
p. 4951-4954 4 p. |
artikel |
36 |
Photogenerated nitrenium ions: Singlet and triplet state reactions of tert-butyl-(2-acetyl-4-methyl)phenyl nitrenium ion
|
Robbins, Rebecca J. |
|
1994 |
35 |
28 |
p. 4943-4946 4 p. |
artikel |
37 |
Pinacol closure of oxygenated taxane skeleta at C-1-C-2 with stereoinduction by oxygen substituents at C-9 and C-10
|
Swindell, Charles S. |
|
1994 |
35 |
28 |
p. 4959-4962 4 p. |
artikel |
38 |
Rapamycin synthetic studies. 1. Construction of the C(27)-C(42) subunit
|
Smith III, Amos B. |
|
1994 |
35 |
28 |
p. 4907-4910 4 p. |
artikel |
39 |
Rapamycin synthetic studies. 2. Elaboration of the C(10)-C(26) perimeter
|
Smith III, Amos B. |
|
1994 |
35 |
28 |
p. 4911-4914 4 p. |
artikel |
40 |
Remote acyclic diastereocontol involving a bicyclic metal chelate. High 1,5 asymmetric induction in the hydride reduction of δ-hydroxy ketones
|
Zhang, Han-Cheng |
|
1994 |
35 |
28 |
p. 4891-4894 4 p. |
artikel |
41 |
Selenium induced stereoselective cyclization of N-substituted-4-hydroxy-5-hexenylamines
|
Cooper, Matthew A. |
|
1994 |
35 |
28 |
p. 5065-5068 4 p. |
artikel |
42 |
SNAr reactions of benzaldimines: A concise synthesis of substituted phenanthridines
|
Reuter, Deborah C. |
|
1994 |
35 |
28 |
p. 4899-4902 4 p. |
artikel |
43 |
Solid-phase synthesis of oligonucleoside methylphosphonate 5′-phosphates
|
Bhan, Purshotam |
|
1994 |
35 |
28 |
p. 4895-4898 4 p. |
artikel |
44 |
Stereoselective synthesis of protected amino alkyl epoxides
|
Romeo, Sergio |
|
1994 |
35 |
28 |
p. 4939-4942 4 p. |
artikel |
45 |
Strigol synthetic studies the first synthetic approach that allows control of C-2′ configuration
|
Frischmuth, Katja |
|
1994 |
35 |
28 |
p. 4973-4976 4 p. |
artikel |
46 |
Structure-enantioselectivity relationships using neural networks for the reduction of carbonyl compounds with baker's yeast
|
Zakarya, D. |
|
1994 |
35 |
28 |
p. 4985-4988 4 p. |
artikel |
47 |
Substituent effect on the solvolysis of α-t-butyl-α-methylbenzyl chlorides
|
Fujio, Mizue |
|
1994 |
35 |
28 |
p. 5005-5008 4 p. |
artikel |
48 |
Synthesis and stereochemical confirmation of the cis-fused L/M and N/O ring systems of maitotoxin
|
Sasaki, Makoto |
|
1994 |
35 |
28 |
p. 5023-5026 4 p. |
artikel |
49 |
Synthesis of both enantiomers of C2 symmetric trans-2,5-bis(hydroxymethyl)pyrrolidine. Lipase mediated sequential kinetic resolutions
|
Sibi, Mukund P. |
|
1994 |
35 |
28 |
p. 4915-4918 4 p. |
artikel |
50 |
Synthesis of novel phosphonate analogue of Kdo as a tool for the design of potent inhibitors for lipopolysaccharide biosynthesis
|
Sheffer-Dee-Noor, Shani |
|
1994 |
35 |
28 |
p. 5077-5080 4 p. |
artikel |
51 |
The first synthesis of vancomycinic acid
|
Rama Rao, AV |
|
1994 |
35 |
28 |
p. 5047-5050 4 p. |
artikel |
52 |
The pauson-khand reaction on carbohydrate templates.I. Synthesis of bis-heteroannulated-pyranosides
|
Marco-Contelles, José |
|
1994 |
35 |
28 |
p. 5059-5062 4 p. |
artikel |
53 |
The reactivity of a surfactant-bound micellar phosphotriester
|
Kotchevar, Ann T. |
|
1994 |
35 |
28 |
p. 4927-4930 4 p. |
artikel |
54 |
Total synthesis of (±)-allo-cedrol [Khusiol]
|
Sathya Shanker, P. |
|
1994 |
35 |
28 |
p. 5055-5058 4 p. |
artikel |
55 |
Triphenylbismuth dibromide-iodine: An efficient reagent for the dehydration of alcohols
|
Dorta, Rosa L. |
|
1994 |
35 |
28 |
p. 5035-5038 4 p. |
artikel |
56 |
Urocanic acid photobiology. Purine-assisted photooxidation to 1H-imidazole-4(5)-carboxaldehyde
|
Mohammad, Taj |
|
1994 |
35 |
28 |
p. 4906- 1 p. |
artikel |