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- Currently displaying 421 - 440 of 1024 publications
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly.
Chemical communications (Cambridge, England)
(2006)
2566
(doi: 10.1039/b600382f)
Practical Synthesis of ( S )-Pyrrolidin-2-yl-1 H -tetrazole, Incorporating Efficient Protecting Group Removal by Flow-Reactor Hydrogenolysis
Synlett
(2006)
2006
889
(doi: 10.1055/s-2006-939036)
Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives
Organic and Biomolecular Chemistry
(2006)
4
1471
(doi: 10.1039/b601888b)
Double Conjugate Addition of Dithiols to Propargylic Carbonyl Systems To Generate Protected 1,3-Dicarbonyl Compounds
The Journal of Organic Chemistry
(2006)
71
2715
(doi: 10.1021/jo052514s)
Preparation of the Neolignan Natural Product Grossamide by a Continuous-Flow Process
Synlett
(2006)
2006
427
(doi: 10.1055/S-2006-926244)
A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane‐1,2‐diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide
Chemistry – A European Journal
(2006)
3
431
(doi: 10.1002/chem.19970030315)
Sexual development of malaria parasites is inhibited in vitro by the Neem extract Azadirachtin, and its semi-synthetic analogues
FEMS microbiology letters
(2006)
120
267
Diastereoselective aldol reactions with butane-2,3-diacetal protected glyceraldehyde derivatives (vol 4, pg 1471, 2006)
ORG BIOMOL CHEM
(2006)
4
1612
Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst.
Chem. Commun.
(2005)
66
(doi: 10.1039/b514636d)
Defects in signal transduction caused by a T cell receptor beta chain substitution.
Eur J Immunol
(2005)
20
1417
(doi: 10.1002/eji.1830200702)
Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
Organic & Biomolecular Chemistry
(2005)
3
4095
(doi: 10.1039/b512410g)
Evolution or Revolution: The Challenge to the Modern Medicinal Chemist
(2005)
1
Total synthesis of two novel subpicomolar sarco/endoplasmatic reticulum Ca2+-ATPase inhibitors designed by an analysis of the binding site of thapsigargin
J Med Chem
(2005)
48
7005
(doi: 10.1021/jm058036v)
Synthesis of Alkaloid Natural Products Using Solid-Supported Reagents and Scavengers
Current Organic Chemistry
(2005)
9
1521
(doi: 10.2174/138527205774370513)
A versatile organocatalyst for the asymmetric conjugate addition of nitroalkanes to enones.
Chemical Communications
(2005)
5346
(doi: 10.1039/b511441a)
A highly selective, organocatalytic route to chiral dihydro-1,2-oxazines.
Org Lett
(2005)
7
4189
(doi: 10.1021/ol051577u)
Total Synthesis of Spongistatin 1: A Synthetic Strategy Exploiting Its Latent Pseudo‐Symmetry
Angewandte Chemie (International ed. in English)
(2005)
44
5433
(doi: 10.1002/anie.200502008)
Non-metal-catalysed intramolecular alkyne cyclotrimerization reactions promoted by focussed microwave heating in batch and flow modes.
Organic & Biomolecular Chemistry
(2005)
3
3365
(doi: 10.1039/b509540a)