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- Currently displaying 401 - 420 of 1025 publications
A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols.
Chem Commun (Camb)
(2006)
4835
(doi: 10.1039/b612197g)
A new asymmetric organocatalytic nitrocyclopropanation reaction
Chemical communications (Cambridge, England)
(2006)
4838
(doi: 10.1039/b612436b)
Sulphuration of Electron-Rich Arenes with Sulphenamides and Aminosulphenyl Chlorides
Synthetic Communications
(2006)
10
291
(doi: 10.1080/00397918008062752)
Polymer-supported reagents and scavengers in synthesis
(2006)
3
791
Fully automated continuous flow synthesis of 4,5-disubstituted oxazoles.
Organic Letters
(2006)
8
5231
(doi: 10.1021/ol061975c)
Stereocontrolled Total Synthesis of Bengazole A: A Marine Bisoxazole Natural Product Displaying Potent Antifungal Properties
Angewandte Chemie (International ed. in English)
(2006)
45
6714
(doi: 10.1002/anie.200602050)
An enantioselective organocatalytic route to chiral 3,6-dihydropyridazines from aldehydes
Synlett
(2006)
2006
2548
(doi: 10.1055/s-2006-951486)
Oxidation of activated halides to aldehydes and ketones by n-methylmorpholine-n-oxide
Synthetic Communications
(2006)
22
1967
(doi: 10.1080/00397919208021328)
ORGN 141-Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst
ABSTR PAP AM CHEM S
(2006)
232
Enantioselective Catalytic Intramolecular Cyclopropanation using Modified Cinchona Alkaloid Organocatalysts
Angewandte Chemie (International ed. in English)
(2006)
45
6024
(doi: 10.1002/anie.200602129)
8,9,10,10a-tetrahydro-6H-tetrazolo[1,5-a]pyrrolo[2,1-c]pyrazines:: New heterocyclic frameworks generated by an Ugi-type multicomponent reaction
Synthesis
(2006)
2006
3215
(doi: 10.1055/s-2006-950219)
Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat (TM) 30NP
Beilstein J Org Chem
(2006)
2
15
(doi: 10.1186/1860-5397-2-15)
A highly selective, organocatalytic route to chiral 1,2-oxazines from ketones.
Chemical Communications
(2006)
3211
(doi: 10.1039/b606338a)
Natural Products as an Inspiration for the Discovery of New High-Throughput Chemical Synthesis Tools
(2006)
2
51
(doi: 10.1002/9780470085226.ch2)
Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations
Chemistry (Weinheim an der Bergstrasse, Germany)
(2006)
12
4407
(doi: 10.1002/chem.200501400)
The Use of Polymer Supported Reagents and Scavengers in the Synthesis of Natural Products
(2006)
131
(doi: 10.1201/9781420009279)
Effect of azadirachtin‐derived decalin (perhydronaphthalene) and dihydrofuranacetal (furo[2, 3‐fo]pyran) fragments on the feeding behaviour of Spodoptera littoralis
Pesticide Science
(2006)
40
169
(doi: 10.1002/ps.2780400212)
Microwave flow chemistry: the next evolutionary step in synthetic chemistry?
Chimica Oggi
(2006)
24
41
Progress towards avermectins and milbemycins
Pesticide Science
(2006)
18
153
(doi: 10.1002/ps.2780180210)
Targeting C-reactive protein for the treatment of cardiovascular disease.
Nature
(2006)
440
1217
(doi: 10.1038/nature04672)