Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chemistry, organic (11) 11
catalysis (9) 9
stereoisomerism (9) 9
index medicus (8) 8
molecular structure (7) 7
article (6) 6
chemistry, multidisciplinary (6) 6
hydrogenation (5) 5
chemical properties (4) 4
derivatives (4) 4
enantiomers (4) 4
aldehydes (3) 3
amines (3) 3
asymmetry (3) 3
catalysts (3) 3
chemistry techniques, synthetic (3) 3
ketones (3) 3
nitriles (3) 3
organic chemistry (3) 3
reagents (3) 3
reduction (3) 3
rheumatoid-arthritis (3) 3
synthesis (3) 3
acyclic or carbocyclic compounds (2) 2
alpha-arylation (2) 2
amide bond formation (2) 2
amides (2) 2
amides - chemical synthesis (2) 2
amides - chemistry (2) 2
asymmetric-synthesis (2) 2
asymmetrische katalyse (2) 2
azid (2) 2
azides (2) 2
benzoates - chemical synthesis (2) 2
benzoates - chemistry (2) 2
carbamate (2) 2
carbamates (2) 2
carbonyl-compounds (2) 2
carboxylic acids - chemistry (2) 2
carboxylic-acids (2) 2
chemical synthesis (2) 2
chemistry (2) 2
chemistry, applied (2) 2
chiralität (2) 2
condensation reactions (2) 2
continuous-flow (2) 2
coupling reagents (2) 2
cycloaddition (2) 2
cyclopropan (2) 2
cyclopropane (2) 2
dearomatization (2) 2
dwell-time (2) 2
efficient synthesis (2) 2
esters (2) 2
green & sustainable science & technology (2) 2
green chemistry (2) 2
hofmann rearrangement (2) 2
imines - chemistry (2) 2
isocyanate (2) 2
isocyanates (2) 2
kontinuierliche strömung (2) 2
lewis base (2) 2
ligands (2) 2
metallurgy (2) 2
methods (2) 2
molecular calculations (2) 2
molecular conformation (2) 2
o-quinone methides (2) 2
organic compounds (2) 2
peptide-synthesis (2) 2
protective-groups (2) 2
reaction-mechanism (2) 2
reaktionsmechanismus (2) 2
rearrangement-reaction (2) 2
research (2) 2
scale-up (2) 2
schiff bases (2) 2
schutzgruppe (2) 2
spiro compounds - chemical synthesis (2) 2
tetrahedrons (2) 2
umlagerungsreaktion (2) 2
verweilzeit (2) 2
-berkelic acid (1) 1
1,4-addition (1) 1
1,8-disubstituted naphthalenes (1) 1
11-beta-hydroxysteroid dehydrogenase type 1 - antagonists & inhibitors (1) 1
11-beta-hydroxysteroid dehydrogenase type 1 - metabolism (1) 1
access (1) 1
accessibility (1) 1
acid (1) 1
aldehyde derivatives (1) 1
aldehyde imines (1) 1
aldol reactions (1) 1
allylation (1) 1
amination, n‐alkylation, n‐arylation (1) 1
aminophosphines (1) 1
analysis (1) 1
annelation (1) 1
anti-meso-acetylmethyldivinylcyclopentane (1) 1
antitubercular agents (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text A General Method for Imine Formation Using B(OCH 2 CF 3 ) 3
by Reeves, Jonathan T and Visco, Michael D and Marsini, Maurice A and Grinberg, Nelu and Busacca, Carl A and Mattson, Anita E and Senanayake, Chris H
Organic Letters, ISSN 1523-7060, 05/2015, Volume 17, Issue 10, pp. 2442 - 2445
Tris(2,2,2-trifluoroethyl)borate [B(OCH2CF3)3] was found to be a mild and general reagent for the formation of a variety of imines by condensation of amides or... 
Hydrocarbons, Fluorinated - chemistry | Molecular Structure | Imines - chemical synthesis | Borates - chemistry | Imines - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Potent and selective CC chemokine receptor 1 antagonists labeled with carbon‐13, carbon‐14, and tritium
by Latli, Bachir and Hrapchak, Matt and Cheveliakov, Maxim and Reeves, Jonathan T and Marsini, Maurice and Busacca, Carl A and Senanayake, Chris H
Journal of Labelled Compounds and Radiopharmaceuticals, ISSN 0362-4803, 08/2018, Volume 61, Issue 10, pp. 764 - 772
1‐(4‐Fluorophenyl)‐1H‐pyrazolo[3,4‐c]pyridine‐4‐carboxylic acid (2‐methanesulfonyl‐pyridin‐4‐ylmethyl)‐amide (1) and its analogs (2) and (3) are potent CCR1... 
radiosynthesis | tritium | carbon‐13 | carbon‐14 | CCR1 antagonists | carbon-14 | carbon-13 | RHEUMATOID-ARTHRITIS | CHEMISTRY, ANALYTICAL | CHEMISTRY, MEDICINAL | BIOCHEMICAL RESEARCH METHODS
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Transnitrilation from Dimethylmalononitrile to Aryl Grignard and Lithium Reagents: A Practical Method for Aryl Nitrile Synthesis
by Reeves, Jonathan T and Malapit, Christian A and Buono, Frederic G and Sidhu, Kanwar P and Marsini, Maurice A and Sader, C. Avery and Fandrick, Keith R and Busacca, Carl A and Senanayake, Chris H
Journal of the American Chemical Society, ISSN 0002-7863, 1900, Volume 137, Issue 29, pp. 9481 - 9488
An electrophilic cyanation of aryl Grignard or lithium reagents, generated in situ from the corresponding aryl bromides or iodides, by a transnitrilation with... 
HALIDES | C-H CYANATION | EXCHANGE-REACTION | MOLECULAR CALCULATIONS | HYDROGENATION | EFFECTIVE CORE POTENTIALS | TERTIARY AMIDE | POTASSIUM HEXACYANOFERRATE(II) | HALOGEN | PALLADIUM-CATALYZED CYANATION | CHEMISTRY, MULTIDISCIPLINARY | Chemistry Techniques, Synthetic | Lithium - chemistry | Nitriles - chemistry | Nitriles - chemical synthesis | Organometallic Compounds - chemistry | Catalysis | Indicators and Reagents - chemistry | Nitriles | Lithium | Research | Chemical properties | Chemical synthesis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text A Practical Procedure for Reduction of Primary, Secondary and Tertiary Amides to Amines
by Reeves, Jonathan T and Tan, Zhulin and Marsini, Maurice A and Han, Zhengxu S and Xu, Yibo and Reeves, Diana C and Lee, Heewon and Lu, Bruce Z and Senanayake, Chris H
Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2013, Volume 355, Issue 1, pp. 47 - 52
A mild and general procedure for reduction of primary, secondary, and tertiary amides using catalytic triruthenium dodecacarbonyl and... 
silanes | ruthenium | amides | reduction | SYSTEM | SELF-ENCAPSULATION | COMPLEX | SILANE REDUCTION | HYDROSILANES | CHEMISTRY, ORGANIC | CONVENIENT | CARBOXAMIDES | CHEMOSELECTIVE REDUCTION | CHIMIE ORGANIQUE | CATALYZED REDUCTION | CHEMISTRY, APPLIED | Amides | Amines | Ruthenium | Silane | Silanes | Reduction | Catalysts | Accessibility | Crystallization | Catalysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text A Diastereoselective Formal Synthesis of Berkelic Acid
by Wenderski, Todd A and Marsini, Maurice A and Pettus, Thomas R. R
Organic Letters, ISSN 1523-7060, 01/2011, Volume 13, Issue 1, pp. 118 - 121
A formal synthesis of berkelic acid is reported. The strategy employs the combination of a chiral exocyclic enol ether and an achiral isochromanone to afford... 
(-)-BERKELIC ACID | CYCLOADDITION | REAGENTS | LACTONES | NATURAL-PRODUCTS | O-QUINONE METHIDES | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | SPIROKETAL | CANCER | Molecular Structure | Cyclization | Oxidation-Reduction | Stereoisomerism | Spiro Compounds - chemical synthesis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Efficient Asymmetric Synthesis of Structurally Diverse P‐Stereogenic Phosphinamides for Catalyst Design
by Han, Zhengxu S and Zhang, Li and Xu, Yibo and Sieber, Joshua D and Marsini, Maurice A and Li, Zhibin and Reeves, Jonathan T and Fandrick, Keith R and Patel, Nitinchandra D and Desrosiers, Jean‐Nicolas and Qu, Bo and Chen, Anji and Rudzinski, DiAndra M and Samankumara, Lalith P and Ma, Shengli and Grinberg, Nelu and Roschangar, Frank and Yee, Nathan K and Wang, Guijun and Song, Jinhua J and Senanayake, Chris H
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2015, Volume 54, Issue 18, pp. 5474 - 5477
The use of chiral phosphinamides is relatively unexplored because of the lack of a general method for the synthesis. Reported herein is the development of a... 
phosphinamides | asymmetric catalysis | organocatalyst | chirality | nucleophilic substitution | Nucleophilic substitution | Organocatalyst | Phosphinamides | Asymmetric catalysis | Chirality | BRONSTED ACID | REAGENTS | AMINOPHOSPHINES | ALDOL REACTIONS | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | ORGANOCATALYSTS | BLOCKS | OXIDES | Phosphines - chemical synthesis | Chemistry Techniques, Synthetic | Phosphines - chemistry | Phosphinic Acids - chemistry | Amides - chemical synthesis | Stereoisomerism | Amides - chemistry | Molecular Structure | Lewis Bases - chemistry | Synthesis | Catalysis | Enantiomers | Organic compounds | Asymmetry | Catalysts | Lewis base
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Diastereoselective syntheses of substituted cis-hydrindanones featuring sequential inter- and intramolecular Michael reactions
by Liu, Junjia and Marsini, Maurice A and Bedell, T. Aaron and Reider, Paul J and Sorensen, Erik J
Tetrahedron, ISSN 0040-4020, 06/2016, Volume 72, Issue 26, pp. 3713 - 3717
The hydrindane (bicyclo[4.3.0]nonane) structural motif ( ) and related -1-hydrindanone skeleton ( ) are common substructures in many natural products. Herein,... 
Hydrindanone | Conjugate addition | Olefin cross metathesis | Michael reaction | 1,4-Addition | Linchpin | MUKAIYAMA | SILYLATED KETENE ACETALS | CHEMISTRY, ORGANIC | DECARBOXYLATION | ANTI-MESO-ACETYLMETHYLDIVINYLCYCLOPENTANE | SILYLKETENE ACETALS | CONSTRUCTION | ANNELATION | BETA-KETO | DERIVATIVES | ACCESS | Chemical industry | Herbicides | Pesticides industry | Incorporation | Copper | Construction standards | Substructures | Construction | Natural products | Tetrahedrons | Strategy | Ketenes | linchpin | olefin cross metathesis | hydrindanone | 1,4-addition | conjugate addition
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Diastereoselective Synthesis of α‑Quaternary Aziridine-2-carboxylates via Aza-Corey–Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters
by Marsini, Maurice A and Reeves, Jonathan T and Desrosiers, Jean-Nicolas and Herbage, Melissa A and Savoie, Jolaine and Li, Zhibin and Fandrick, Keith R and Sader, C. Avery and McKibben, Bryan and Gao, Donghong A and Cui, Jianwen and Gonnella, Nina C and Lee, Heewon and Wei, Xudong and Roschangar, Frank and Lu, Bruce Z and Senanayake, Chris H
Organic Letters, ISSN 1523-7060, 11/2015, Volume 17, Issue 22, pp. 5614 - 5617
A general, scalable, and highly diastereoselective aziridination of N-tert-butanesulfinyl ketimino esters is described. The methodology has been utilized to... 
Stereoisomerism | Aza Compounds - chemistry | Esters | Molecular Structure | Catalysis | Aziridines - chemistry | Aziridines - chemical synthesis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Triisopropyl borate mediated N-sulfinyl imine formation
by Visco, Michael D and Reeves, Jonathan T and Marsini, Maurice A and Volchkov, Ivan and Busacca, Carl A and Mattson, Anita E and Senanayake, Chris H
Tetrahedron Letters, ISSN 0040-4039, 04/2016, Volume 57, Issue 17, pp. 1903 - 1905
Triisopropyl borate effects the condensation of aldehydes with sulfinamides to give -sulfinyl imines. The reaction is amenable to 1°, 2°, and 3° alkyl... 
Imine | Borate | Condensation | Sulfinamide | KETONES | ASYMMETRIC-SYNTHESIS | AMINES | TERT-BUTANESULFINYL KETIMINES | CHEMISTRY, ORGANIC | ALDEHYDES | Aldehydes | Schiff bases | Borates | Filtration | Imines | Reagents | Tetrahedrons | Byproducts
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Sequential C–H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD‑1 Inhibitor
by Wei, Xudong and Qu, Bo and Zeng, Xingzhong and Savoie, Jolaine and Fandrick, Keith R and Desrosiers, Jean-Nicolas and Tcyrulnikov, Sergei and Marsini, Maurice A and Buono, Frederic G and Li, Zhibin and Yang, Bing-Shiou and Tang, Wenjun and Haddad, Nizar and Gutierrez, Osvaldo and Wang, Jun and Lee, Heewon and Ma, Shengli and Campbell, Scot and Lorenz, Jon C and Eckhardt, Matthias and Himmelsbach, Frank and Peters, Stefan and Patel, Nitinchandra D and Tan, Zhulin and Yee, Nathan K and Song, Jinhua J and Roschangar, Frank and Kozlowski, Marisa C and Senanayake, Chris H
Journal of the American Chemical Society, ISSN 0002-7863, 11/2016, Volume 138, Issue 47, pp. 15473 - 15481
A concise asymmetric synthesis of an 11β-HSD-1 inhibitor has been achieved using inexpensive starting materials with excellent step-economy at low catalyst... 
MECHANISTIC INVESTIGATIONS | MOLECULAR CALCULATIONS | LIGANDS | IRIDIUM COMPLEXES | BOND FORMATION | PYRIDINIUM SALTS | SUBSTITUTED PIPERIDINES | MULTIPLE STEREOGENIC CENTERS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | CATALYZED DIRECT ARYLATION | Piperidines - chemistry | Stereoisomerism | Humans | Molecular Conformation | Enzyme Inhibitors - pharmacology | Enzyme Inhibitors - chemical synthesis | Piperidines - chemical synthesis | 11-beta-Hydroxysteroid Dehydrogenase Type 1 - antagonists & inhibitors | Hydrogenation | 11-beta-Hydroxysteroid Dehydrogenase Type 1 - metabolism | Piperidines - pharmacology | Enzyme Inhibitors - chemistry | Catalysis | Iridium - chemistry | Palladium - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement
by Marsini, Maurice A and Buono, Frederic G and Lorenz, Jon C and Yang, Bing-Shiou and Reeves, Jonathan T and Sidhu, Kanwar and Sarvestani, Max and Tan, Zhulin and Zhang, Yongda and Li, Ning and Lee, Heewon and Brazzillo, Jason and Nummy, Laurence J and Chung, J. C and Luvaga, Irungu K and Narayanan, Bikshandarkoil A and Wei, Xudong and Song, Jinhua J and Roschangar, Frank and Yee, Nathan K and Senanayake, Chris H
Green Chemistry, ISSN 1463-9262, 2017, Volume 19, Issue 6, pp. 1454 - 1461
A convergent, robust, and concise synthesis of a developmental CCR1 antagonist is described using continuous flow technology. In the first approach, following... 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement
by Marsini, MA and Buono, FG and Lorenz, JC and Yang, BS and Reeves, JT and Sidhu, K and Sarvestani, M and Tan, ZL and Zhang, YD and Li, N and Lee, H and Brazzillo, J and Nummy, LJ and Chung, JC and Luvaga, IK and Narayanan, BA and Wei, XD and Song, JHJ and Roschangar, F and Yee, NK and Senanayake, CH
GREEN CHEMISTRY, ISSN 1463-9262, 03/2017, Volume 19, Issue 6, pp. 1454 - 1461
A convergent, robust, and concise synthesis of a developmental CCR1 antagonist is described using continuous flow technology. In the first approach, following... 
RHEUMATOID-ARTHRITIS | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | SCALE-UP | ALPHA-ARYLATION | HOFMANN REARRANGEMENT | GREEN CHEMISTRY | EFFICIENT SYNTHESIS | COUPLING REAGENTS | AMIDE BOND FORMATION | PEPTIDE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | CARBOXYLIC-ACIDS | Coupling (molecular) | Trapping | Synthesis | Cyclopropane | Transformations | Robustness | Continuous flow | Extreme values
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Diastereoselective Syntheses of Chroman Spiroketals via [4 + 2] Cycloaddition of Enol Ethers and o-Quinone Methides
by Marsini, Maurice A and Huang, Yaodong and Lindsey, Christopher C and Wu, Kun-Liang and Pettus, Thomas R. R
Organic Letters, ISSN 1523-7060, 04/2008, Volume 10, Issue 7, pp. 1477 - 1480
A variety of chroman spiroketals are synthesized via inverse-demand [4 + 2] cycloaddition of enol ethers and ortho-quinone methides (o-QMs). Low temperature... 
CHEMISTRY, ORGANIC | ACID | RUBROMYCINS | NITRILES | COMPLEXES | Biological Products - chemical synthesis | Stereoisomerism | Spiro Compounds - chemical synthesis | Chromans - chemical synthesis | Ethers - chemistry | Indolequinones - chemistry | Molecular Structure | Furans - chemical synthesis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Full Text Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangementElectronic supplementary information (ESI) available. See DOI: 10.1039/c6gc03123d
by Marsini, Maurice A and Buono, Frederic G and Lorenz, Jon C and Yang, Bing-Shiou and Reeves, Jonathan T and Sidhu, Kanwar and Sarvestani, Max and Tan, Zhulin and Zhang, Yongda and Li, Ning and Lee, Heewon and Brazzillo, Jason and Nummy, Laurence J and Chung, J. C and Luvaga, Irungu K and Narayanan, Bikshandarkoil A and Wei, Xudong and Song, Jinhua J and Roschangar, Frank and Yee, Nathan K and Senanayake, Chris H
ISSN 1463-9262, 3/2017, Volume 19, Issue 6, pp. 1454 - 1461
A convergent, robust, and concise synthesis of a developmental CCR1 antagonist is described using continuous flow technology. In the first approach, following... 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
15. Full Text Carbamoyl Anion Addition to N‑Sulfinyl Imines: Highly Diastereoselective Synthesis of α‑Amino Amides
by Reeves, Jonathan T and Tan, Zhulin and Herbage, Melissa A and Han, Zhengxu S and Marsini, Maurice A and Li, Zhibin and Li, Guisheng and Xu, Yibo and Fandrick, Keith R and Gonnella, Nina C and Campbell, Scot and Ma, Shengli and Grinberg, Nelu and Lee, Heewon and Lu, Bruce Z and Senanayake, Chris H
Journal of the American Chemical Society, ISSN 0002-7863, 04/2013, Volume 135, Issue 15, pp. 5565 - 5568
Carbamoyl anions, generated from N,N-disubstituted formamides and lithium diisopropylamide, add with high diastereoselectivity to chiral N-sulfinyl aldimines... 
ORGANIC-SYNTHESIS | KETONES | ASYMMETRIC-SYNTHESIS | ORGANOMETALLIC REAGENTS | NUCLEOPHILIC ACYLATION | ALDEHYDE IMINES | REACTIVITY | MAIN-GROUP METAL | CARBONYL-COMPOUNDS | UMPOLUNG | CHEMISTRY, MULTIDISCIPLINARY | Chemistry Techniques, Synthetic | Amides - chemical synthesis | Stereoisomerism | Molecular Conformation | Imines - chemistry | Amides - chemistry | Models, Molecular | Substrate Specificity | Dipeptides - chemical synthesis | Dipeptides - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
16. Full Text Sequential C-H arylation and enantioselective hydrogenation enables ideal asymmetric entry to the indenopiperidine core of an 11beta-HSD-1 inhibitor
by Senanayake, Chris H and Kozlowski, Marisa C and Zeng, Xingzhong and Wei, Xudong and Qu, Bo and Savoie, Jolaine and Fandrick, Keith R and Tcyrulnikov, Sergei and Desrosiers, Jean-Nicolas and Marsini, Maurice A and Buono, Frederic G and Li, Zhibin and Yang, Bing-Shiou and Tang, Wenjun and Haddad, Nizar and Gutierrez, Osvaldo and Wang, Jun and Lee, Heewon and Ma, Shengli and Campbell, Scot and Lorenz, Jon C and Eckhardt, Matthias and Himmelsbach, Frank and Peters, Stefan and Patel, Nitinchandra D and Tan, Zhulin and Yee, Nathan K and Song, Jinhua J and Roschangar, Frank
Journal of the American Chemical Society, ISSN 0002-7863, 11/2016, Volume 138, Issue 47, p. 15473
Usage | Chemical properties | Chemical synthesis | Hydrogenation | Chemical compounds
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
17. Full Text Total Synthesis of (±)-Mitorubrinic Acid
by Marsini, Maurice A and Gowin, Kristoffer M and Pettus, Thomas R. R
Organic Letters, ISSN 1523-7060, 08/2006, Volume 8, Issue 16, pp. 3481 - 3483
(±)-Mitorubrinic acid, a member of the azaphilone family of natural products, has been constructed in 12 steps. Key aspects of the synthesis include... 
FUNGI | PENICILLIUM-FUNICULOSUM | AZAPHILONES | CHEMISTRY, ORGANIC | CYCLOISOMERIZATION | MITORUBRIN | METABOLITE | DEAROMATIZATION
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
18. Full Text A Concise and Convergent Synthesis of PA-824
by Marsini, Maurice A and Reider, Paul J and Sorensen, Erik J
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2010, Volume 75, Issue 21, pp. 7479 - 7482
An efficient four-step synthesis of PA-824, a promising antituberculosis drug candidate, has been developed. This concise approach offers significant... 
MYCOBACTERIUM-TUBERCULOSIS | CHEMISTRY, ORGANIC | MURINE MODEL | NITROIMIDAZOPYRAN DRUG CANDIDATE | VOLTAMMETRIC DETERMINATION | REDUCTION | Hydrolysis | Antitubercular Agents - chemical synthesis | Nitroimidazoles - chemical synthesis | Antitubercular Agents - chemistry | Nitroimidazoles - pharmacology | Stereoisomerism | Drug Resistance, Multiple - drug effects | Antitubercular Agents - pharmacology | Kinetics | Nitroimidazoles - chemistry | Antitubercular agents | Chemical properties | Research | Pharmaceutical chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
19. Full Text Chemoselective Reactions of 3-Benzyloxy-1,2-o-Quinone with Organometallic Reagents
by Miller, Luke A and Marsini, Maurice A and Pettus, Thomas R. R
Organic Letters, ISSN 1523-7060, 05/2009, Volume 11, Issue 9, pp. 1955 - 1958
Chemoselective additions of organometallic reagents to 3-benzyloxy-1,2-o-quinone are described. Various nucleophiles are shown to undergo selective... 
OXIDATION | ORTHO-QUINONES | CYCLOADDITION | DIELS-ALDER REACTIONS | ENANTIOSELECTIVE SYNTHESIS | O-BENZOQUINONES | REDUCTION | LEWIS-ACID | ALLYLATION | CHEMISTRY, ORGANIC | DERIVATIVES
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
20. Full Text Carbamoyl Anion Addition toN-Sulfinyl Imines: Highly Diastereoselective Synthesis of α-Amino Amides
by Reeves, Jonathan T and Tan, Zhulin and Herbage, Melissa A and Han, Zhengxu S and Marsini, Maurice A and Li, Zhibin and Li, Guisheng and Xu, Yibo and Fandrick, Keith R and Gonnella, Nina C and Campbell, Scot and Ma, Shengli and Grinberg, Nelu and Lee, Heewon and Lu, Bruce Z and Senanayake, Chris H
Journal of the American Chemical Society, ISSN 0002-7863, 04/2013, Volume 135, Issue 15, pp. 5565 - 5568
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.