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ORGANIC LETTERS, ISSN 1523-7060, 08/2019, Volume 21, Issue 15, pp. 5962 - 5966
A simple and efficient approach to enantioenriched alpha,beta-disubstituted gamma-butyrolactones has been developed through multifunctional modular... 
OXY-MICHAEL ADDITION | COOPERATIVE CATALYSIS | LACTONES | ACIDS | ANNULATION | CHEMISTRY, ORGANIC | LACTAMS | STEREOSELECTIVE-SYNTHESIS | ACCESS | ENALS
Journal Article
Asian Journal of Organic Chemistry, ISSN 2193-5807, 06/2019, Volume 8, Issue 6, pp. 814 - 818
Herein, we present a novel enantioselective hemiacetalization/intramolecular oxy‐Michael addition cascade for the synthesis of syn‐1,3‐diol frameworks via... 
syn-1,3-dioxane | kinetic resolution | chiral phosphoric acid | 1,3-polyol | oxy-Michael addition | BRONSTED ACID | ALDOL | ENANTIOSELECTIVE SYNTHESIS | NATURAL-PRODUCTS | CHEMISTRY, ORGANIC | STEREOSELECTIVE TOTAL-SYNTHESIS | 1,5-ASYMMETRIC INDUCTION | ATORVASTATIN | CYCLOETHERIFICATION | CONJUGATE ADDITION
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 04/2019, Volume 21, Issue 8, pp. 2688 - 2692
An organocatalytic method for the asymmetric synthesis of syn-1,3-dioxanes as protected 1,3-diols via dynamic kinetic resolution of in situ generated chiral... 
ALDOL | OXY-MICHAEL ADDITION | REDUCTION | CHEMISTRY, ORGANIC | STEREOSELECTIVE-SYNTHESIS | ENANTIOSELECTIVE CARBONYL ALLYLATION | CONJUGATE ADDITION
Journal Article
Organic Letters, ISSN 1523-7060, 2019, Volume 21, Issue 7, pp. 2156 - 2160
The organocatalytic enantio- and diastereoselective cycloetherification of in situ generated cyanohydrins through the concomitant construction of three chiral... 
OXY-MICHAEL ADDITION | DOMINO REACTIONS | ORGANOCATALYSTS | NATURAL-PRODUCTS | STRATEGY | CHEMISTRY, ORGANIC | ACYL TRANSFER | THIOL ESTERS | ALDEHYDES | ENANTIOSELECTIVE DESYMMETRIZATION | SPIROKETALS
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 01/2019, Volume 14, Issue 1, pp. 116 - 120
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 12/2018, Volume 360, Issue 24, pp. 4710 - 4714
Journal Article
Synthesis, ISSN 0039-7881, 11/2018, Volume 50, Issue 21, pp. 4243 - 4253
Abstract Attempts to obtain enantiomerically enriched tetrahydrofuran derivatives via an intramolecular oxy -Michael addition reaction of ε-hydroxyenone is... 
feature | asymmetric synthesis | bifunctional catalyst | tetrahydrofuran | kinetic resolution | oxy-Michael reaction | organocatalyst | tetrahydropyran | CATALYSIS | ACTIVATION | NATURAL-PRODUCTS | CHEMISTRY, ORGANIC | DONORS | SPIROKETALS | SECONDARY ALCOHOLS | RECENT PROGRESS | CHIRAL BRONSTED ACID | OXA-MICHAEL REACTION
Journal Article
Organic Letters, ISSN 1523-7060, 06/2018, Volume 20, Issue 11, pp. 3259 - 3262
A novel enantioselective bromolactonization of alpha,beta-unsaturated ketones using bifunctional amino-urea catalysts has been developed. The scope of the... 
LEWIS-BASE CATALYSIS | ALKENES | BROMOETHERIFICATION | ACTIVATION | OXY-MICHAEL ADDITION | ASYMMETRIC BROMOLACTONIZATION | THIOUREA ORGANOCATALYSTS | CHEMISTRY, ORGANIC | IODOLACTONIZATION | BROMOCYCLIZATION | BROMOAMINOCYCLIZATION
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 04/2018, Volume 13, Issue 7, pp. 740 - 753
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1397 - 7
Journal Article
Beilstein Journal of Organic Chemistry, ISSN 1860-5397, 08/2017, Volume 13, Issue 1, pp. 1518 - 1523
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 07/2017, Volume 2017, Issue 25, pp. 3631 - 3634
A one‐pot, two‐step l‐proline‐mediated stereoselective α‐C(sp2)–H fluorination of α,β‐unsaturated aldehydes towards their corresponding... 
Synthetic methods | Fluorine | One‐pot reactions | Diastereoselectivity | Fluorinated compounds | One-pot reactions | DESIGN | OXY-MICHAEL ADDITION | MECHANISM | CHEMISTRY, ORGANIC | ALCOHOLS | FACILE | ALPHA-FLUORO-ALPHA,BETA-UNSATURATED ESTERS | EFFICIENT
Journal Article
Chemistry Letters, ISSN 0366-7022, 11/2016, Volume 45, Issue 11, pp. 1300 - 1303
In this study, novel asymmetric cycloetherification via the kinetic resolution of secondary or tertiary alcohols using chiral phosphoric acid catalysts was... 
Organocatalyst | Asymmetric cycloetherification | Tetrahydropyran (THP) | OXY-MICHAEL ADDITION | NATURAL-PRODUCTS | BOND-FORMING REACTIONS | STRONGER BRONSTED ACIDS | TRANSFER HYDROGENATION | AMINOTHIOUREA CATALYSTS | CHEMISTRY, MULTIDISCIPLINARY | BIFUNCTIONAL ORGANOCATALYSTS | SECONDARY ALCOHOLS | MANNICH REACTIONS | RECENT PROGRESS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2016, Volume 55, Issue 25, pp. 7121 - 7125
The first total synthesis of cannabimovone from Cannabis sativa and anhydrocannabimovone was achieved by means of a highly stereoselective gold(I)‐catalyzed... 
gold | cannabinoids | oxy-Michael reaction | total synthesis | cycloisomerization | REVISION | CANNABIDIOL | GOLD CATALYSIS | CHEMICAL-SHIFTS | CHEMISTRY, MULTIDISCIPLINARY | PREDICTION | SPASTICITY | CYCLIZATIONS | MULTIPLE-SCLEROSIS | DELTA-9-TETRAHYDROCANNABINOL | Marijuana | Synthesis | Organic compounds | Gold | Cannabis | Chemical synthesis | Isomerization | Communications | Communication
Journal Article
Organic Letters, ISSN 1523-7060, 12/2015, Volume 17, Issue 24, pp. 6058 - 6061
The first catalytic asymmetric intermolecular alcohol conjugate addition to o-quinone methides (o-QMs) is disclosed. Due to reversible C-O bond formation and... 
BRONSTED ACID | DIRECTING GROUP | CATALYSIS | ACTIVATION | OXY-MICHAEL ADDITION | ENANTIOSELECTIVE SYNTHESIS | DIASTEREOSELECTIVE SYNTHESIS | AEROBIC DIALKOXYLATION | CHEMISTRY, ORGANIC | IN-SITU | CONJUGATE ADDITION
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2015, Volume 54, Issue 51, pp. 15497 - 15500
Journal Article