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Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2019, Volume 361, Issue 12, pp. 2849 - 2854
Herein, we report a p‐toluenesulfonic acid (PTSA) initiated mild and user‐friendly ring opening/domino ring opening cyclization reaction (depends on... 
Cyclopropane | Aniline | Ring opening
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 08/2016, Volume 2016, Issue 23, pp. 4059 - 4066
A straightforward approach for the synthesis of isoxazolidines through MgI2‐catalyzed [3+2] cycloaddition reactions of donor–acceptor cyclopropanes with in... 
Lewis acids | Cycloaddition | Synthetic methods | Nitrogen heterocycles
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2017, Volume 359, Issue 21, pp. 3848 - 3854
Lewis acid catalyzed formal [3+2] cycloadditions of 1‐azadienes with donor acceptor cyclopropanes to synthesize varieties of imine functionalized cyclopentanes... 
azabicyclo[3.2.1]octane | Donor-Acceptor Cyclopropane | Imine Functionalized Cyclopentanes | Pyrrolidine | 1-Azadienes | RING EXPANSION | ANNULATION | ANALOGS | REACTIVITY | CHEMISTRY, ORGANIC | EPOXIDES | DIASTEREOSELECTIVE SYNTHESIS | CHEMISTRY | CHEMISTRY, APPLIED | Alkaloids | Cyclopropane compounds | Lewis acid | Cycloaddition | Derivatives | Chemical synthesis | Organic compounds
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2018, Volume 360, Issue 19, pp. 3687 - 3692
An unexpected MgI2‐promoted [2+4] cycloaddition reaction of in‐situ generated 2‐styrylmalonate from donor‐acceptor cyclopropanes with chalconimines to... 
indenopyridine | 2-styrylmalonate | donor-acceptor cyclopropanes | chalconimines | ROUTE | DIELS-ALDER REACTIONS | ANALOGS | COMPLEXES | POTENTIAL ANTIDEPRESSANTS | CHEMISTRY, ORGANIC | MJ-III-65 NSC-706744 | 4+2 ANNULATION | CHEMISTRY, APPLIED | Derivatives (Financial instruments) | Substitutes | Amides | Cycloaddition | Derivatives | Chemical synthesis | Organic compounds
Journal Article
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, ISSN 1434-193X, 08/2016, Volume 2016, Issue 23, pp. 4059 - 4066
A straightforward approach for the synthesis of isoxazolidines through MgI2-catalyzed [3+2] cycloaddition reactions of donor-acceptor cyclopropanes with in... 
INSERTION | ENANTIOSELECTIVE SYNTHESIS | DIPOLAR CYCLOADDITION | NITROSO ALDOL SYNTHESIS | Lewis acids | CHEMISTRY, ORGANIC | ALDEHYDES | Cycloaddition | Nitrogen heterocycles | DIASTEREOSELECTIVE SYNTHESIS | TETRAHYDROFURANS | RING | DIELS-ALDER REACTION | Synthetic methods | STEREOSELECTIVE-SYNTHESIS
Journal Article
ISSN 1477-0520, 6/2017, Volume 15, Issue 24, pp. 5182 - 519
Lewis acid catalyzed [3 + 3] annulation of N -tosylaziridinedicarboxylates and oxiranes with in situ generated mercaptoaldehyde for the synthesis of... 
Journal Article
Organic Letters, ISSN 1523-7060, 01/2017, Volume 19, Issue 2, pp. 304 - 307
Lewis acid catalyzed [3 + 2]-cycloaddition reaction of donor–acceptor cyclopropanes with vinyl azides has been developed to obtain diastereomerically enriched... 
CHEMISTRY, ORGANIC | ANNULATION | ANALOGS | CONSTRUCTION | ALKALOIDS
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 03/2017, Volume 2017, Issue 12, pp. 1647 - 1656
Substituent and Lewis acid promoted generation of functionalized enolates from epoxides is developed. Divergent attack of the enolate on donor‐acceptor... 
Synthetic methods | Oxygen heterocycles | Epoxides | Enols | Annulation | Enolates
Journal Article
ISSN 1477-0520, 9/2019, Volume 17, Issue 35, pp. 8149 - 8152
A MgI 2 catalyzed formal [3 + 2] cycloaddition reaction between donor-acceptor cyclopropanes and N -sulfonyl 1-azadienes towards the synthesis of highly... 
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 06/2019, Volume 2019, Issue 23, pp. 3806 - 3814
Journal Article
Organic & Biomolecular Chemistry, ISSN 1477-0520, 01/2019, Volume 17, Issue 35, pp. 8149 - 8152
A MgI2 catalyzed formal [3 + 2] cycloaddition reaction between donor–acceptor cyclopropanes and N-sulfonyl 1-azadienes towards the synthesis of highly... 
Cycloaddition | Benzofuran | Cyclopentane | Derivatives | Crystallography | Aluminum oxide | Organic compounds | Exploitation
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2015, Volume 2015, Issue 11, pp. 2517 - 2523
A Lewis‐acid‐catalysed tandem Meinwald rearrangement/[3+2]‐cycloaddition of epoxides with donor–acceptor cyclopropanes to synthesize varieties of... 
Small ring ­systems | Asymmetric synthesis | Cyclization | Oxygen heterocycles | Epoxides | Small ring systems | ANNULATIONS | ENANTIOSELECTIVE SYNTHESIS | NITRONES | ROUTES | CHEMISTRY, ORGANIC | ALDEHYDES | 3+2 CYCLOADDITION | REARRANGEMENT | DIASTEREOSELECTIVE SYNTHESIS | CONSTRUCTION | Hydrolysis | Furans | Synthesis | Enantiomers | Organic compounds
Journal Article
RSC Advances, ISSN 2046-2069, 2014, Volume 4, Issue 63, pp. 33236 - 33244
We have developed a one-pot synthesis of polycyclic fused dispiro-oxindole derivatives by the [3 + 3]-cycloaddition (dimerization) of azomethine ylide derived... 
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2019, Volume 361, Issue 12, pp. 2849 - 2854
Herein, we report a p‐toluenesulfonic acid (PTSA) initiated mild and user‐friendly ring opening/domino ring opening cyclization reaction (depends on... 
metal-free ring opening cyclization | cyclopropane carbaldehyde | N-benzyl aniline | benzo[b]azepine | DONOR-ACCEPTOR CYCLOPROPANES | ACID | CHEMISTRY, ORGANIC | SUBSTITUTED CYCLOPROPANE | CHEMISTRY, APPLIED | ALKYNES | 3+2 CYCLOADDITION | Aniline | Environmental aspects | Cyclopropane compounds
Journal Article
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