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Nature, ISSN 0028-0836, 08/2018, Volume 560, Issue 7718, pp. 350 - 354
Prized for their ability to rapidly generate chemical complexity by building new ring systems and stereocentres(1), cycloaddition reactions have featured in... 
POTENT | REDOX-ACTIVE ESTERS | MULTIDISCIPLINARY SCIENCES | EPOTHILONES | Ring formation (Chemistry) | Research | Drug discovery | Carbon-carbon composites | Cross coupling | Chemical reactions | Hybridization | Enantiomers | Kinases | Modularity | Carbon | Complexity | Organic chemistry | Chemistry | Cycloaddition | Teaching methods | Natural products | Chemical synthesis | Coupling methods | Index Medicus
Journal Article
Organic Letters, ISSN 1523-7060, 01/2012, Volume 14, Issue 2, pp. 660 - 663
A concise, stereoselective, and scalable synthesis of the C20-C26 building block of halichondrins and Eribulin is reported. The synthesis relies on three key... 
NORHALICHONDRIN-B | PRACTICAL SYNTHESIS | SEGMENT | RING | COUPLING REACTION | CONSTRUCTION | CHEMISTRY, ORGANIC | ALDEHYDES | ANTITUMOR POLYETHER MACROLIDES | MARINE SPONGE | Ethers, Cyclic - chemical synthesis | Molecular Structure | Furans - chemical synthesis | Ketones - chemical synthesis | Macrolides | Stereoisomerism | Index Medicus
Journal Article
Journal Article
Astrophysical Journal, ISSN 0004-637X, 06/2017, Volume 842, Issue 2, p. 74
Journal Article
Organic Letters, ISSN 1523-7060, 2008, Volume 10, Issue 16, pp. 3381 - 3384
Journal Article
Organic Letters, ISSN 1523-7060, 10/2006, Volume 8, Issue 22, pp. 5149 - 5152
Journal Article
Proceedings of Science, 2017
Conference Proceeding
Proceedings of Science, 2017
Conference Proceeding
Angewandte Chemie (International ed. in English), ISSN 1433-7851, 12/2010, Volume 49, Issue 49, pp. 9492 - 9495
The first syntheses of Jadomycin A and the carbosugar analogue of Jadomycin B have been achieved in 6 and 20 longest linear steps respectively. The key ring... 
Jadomycin | de novo synthesis | carbasugar | 6π-electrocyclic ring-closure
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 2009, Volume 74, Issue 16, pp. 5961 - 5966
A highly divergent de novo asymmetric synthesis of benzyl alpha-6-deoxyaltropyranoside, benzyl alpha-ascarylopyranoside, benzyl alpha-amicetopyranoside, and... 
ENANTIOSELECTIVE DIHYDROXYLATION REACTIONS | CONVERSION | ANALOGS | MANNOSE | CHEMISTRY, ORGANIC | ITERATIVE DIHYDROXYLATION | SUGARS | L-HEXOSES | PALLADIUM-CATALYZED GLYCOSYLATION | DIGITOXIN | Furans - chemistry | Stereoisomerism | Glycosides - chemical synthesis | Glycosylation | Catalysis | Glycosides - chemistry | Palladium - chemistry | Hexoses - chemistry | Index Medicus
Journal Article
Organic Letters, ISSN 1523-7060, 07/2010, Volume 12, Issue 13, pp. 2986 - 2989
Journal Article
Synthesis, ISSN 0039-7881, 10/2008, Volume 2008, Issue 19, pp. 3171 - 3179
Abstract The stereoselective syntheses of three cyclitols, 5a-carba-α-D-rhamnopyranose, 5a-carba-β-D-digitoxopyranose, and 5a-carba-α-L-rhamnopyranose, have... 
special topic | Carbasugar | Cyclopropanol | Cyclitol | Pd/C hydrogenation | Ring opening | OLIGOSACCHARIDES | DE-NOVO SYNTHESIS | CYCLOPROPANOLS | CHEMISTRY, ORGANIC | ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS | STEP | carbasugar | GLYCOSYLATION REACTION | CARBASUGARS | CYCLOADDITION | ring opening | ENANTIOSELECTIVE DIHYDROXYLATION REACTIONS | ALLYLIC ALCOHOLS | cyclopropanol | cyclitol
Journal Article
Organic Letters, ISSN 1523-7060, 11/2014, Volume 16, Issue 21, pp. 5560 - 5563
Journal Article
ACS Medicinal Chemistry Letters, ISSN 1948-5875, 01/2015, Volume 6, Issue 1, pp. 95 - 99
The Ser/Thr protein kinase, RSK, is associated with oncogenesis, and therefore, there are ongoing efforts to develop RSK inhibitors that are suitable for use... 
RSK inhibition | de novo synthesis | SL0101 | cyclitol | Ser/Thr protein kinase | CHEMISTRY, MEDICINAL | ASYMMETRIC-SYNTHESIS | ANTHRAX TETRASACCHARIDE | DE-NOVO SYNTHESIS | ALKYLATION | IDENTIFICATION | RSK2 INHIBITORS | DIHYDROXYLATION | KINASE RSK | CATALYZED GLYCOSYLATION REACTION | REVEALS
Journal Article
天文和天体物理学研究:英文版, ISSN 1674-4527, 2016, Volume 16, Issue 2, pp. 105 - 112
Journal Article
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