Serra et al., 2016 - Google Patents
d-Penicillamine and l-cysteine derived thiazolidine catalysts: an efficient approach to both enantiomers of secondary alcoholsSerra et al., 2016
View PDF- Document ID
- 15594148887443571652
- Author
- Serra M
- Costa D
- Murtinho D
- Tavares N
- e Melo T
- Publication year
- Publication venue
- Tetrahedron
External Links
Snippet
Abstract d-Penicillamine derived thiazolidine ligands were prepared in a two-step synthetic sequence and used in the enantioselective alkylation of a variety of aromatic aldehydes with diethylzinc at room temperature. Excellent ee, up to> 99%, and nearly complete conversions …
- VVNCNSJFMMFHPL-VKHMYHEASA-N Penicillamine 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CC(C)(S)[C@@H](N)C(O)=O 0 title abstract description 18
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2101/16—The ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/06—Systems containing only non-condensed rings with a five-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2102/00—Systems containing two condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
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Teng et al. | Cu (I)-catalyzed regio-and stereoselective [6+ 3] cycloaddition of azomethine ylides with tropone: an efficient asymmetric access to bridged azabicyclo [4.3. 1] decadienes | |
Denmark et al. | Lewis base activation of Lewis acids: catalytic, enantioselective vinylogous aldol addition reactions | |
Togni | Asymmetric hetero Diels-Alder reactions catalyzed by novel chiral vanadium (IV) bis (1, 3-diketonato) complexes | |
Muramulla et al. | A new catalytic mode of the modularly designed organocatalysts (MDOs): enantioselective synthesis of dihydropyrano [2, 3-c] pyrazoles | |
Ablialimov et al. | Synthesis, structure, and catalytic activity of new ruthenium (II) indenylidene complexes bearing unsymmetrical N-heterocyclic carbenes | |
Fries et al. | Functionalized Tetrahydrofurans from Alkenols and Olefins/Alkynes via Aerobic Oxidation− Radical Addition Cascades | |
Rossi et al. | Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions | |
Kowalczyk et al. | Asymmetric Henry reaction catalyzed by chiral secondary diamine-copper (II) complexes | |
Strand et al. | Asymmetric induction afforded by chiral azolylidene N-heterocyclic carbenes (NHC) catalysts | |
de Vries et al. | Diastereoselective synthesis of pyridyl substituted thiazolidin-4-ones. New ligands for the Cu (I) catalyzed asymmetric conjugate addition of diethylzinc to enones | |
Rafiński et al. | Highly efficient synthesis of spirocyclic (1R)-camphor-derived triazolium salts: Application in the catalytic asymmetric benzoin condensation | |
Wu et al. | Regulation of the flexibility of planar chiral [2.2] paracyclophane ligands and its significant impact on enantioselectivity in asymmetric reactions of diethylzinc with carbonyl compounds | |
Blay et al. | Enantioselective addition of terminal alkynes to N-(diphenylphosphinoyl) imines catalyzed by Zn–BINOL complexes | |
Chen et al. | Highly efficient direct a larger-scale aldol reactions catalyzed by a flexible prolinamide based-metal Lewis acid bifunctional catalyst in the presence of water | |
Motoyama et al. | Formation of Fischer carbene complexes in asymmetric aldol-type condensation of an isocyanide component on bis (oxazolinyl) phenylrhodium (III) complexes with aldehydes: Stereochemistry, structural characterization, and mechanistic studies | |
Fu et al. | Synthesis of novel C2-symmetric chiral bis (oxazoline) ligands and their application in the enantioselective addition of diethylzinc to aldehydes | |
Du et al. | One catalyst for two distinct reactions: sequential asymmetric hetero Diels–Alder reaction and diethylzinc addition | |
Lin et al. | Formal Enantioselective Total Synthesis of Schulzeines A–C via Pd–Catalyzed Intramolecular Asymmetric Allylic Amination | |
Enders et al. | Asymmetric intermolecular Stetter reactions of aromatic heterocyclic aldehydes with arylidenemalonates | |
Llamas et al. | Copper (I)-catalyzed enantioselective 1, 3-dipolar cycloaddition of azomethine ylides with vinyl sulfones | |
Braga et al. | New C2-symmetric chiral disulfide ligands derived from (R)-cysteine | |
Wu et al. | Design of C2-symmetric salen ligands and their Co (II)-or Yb (III)-complexes, and their role in the reversal of enantioselectivity in the asymmetric Henry reaction | |
Hsu et al. | Construction of spirofused tricyclic frameworks by NHC-catalyzed intramolecular Stetter reaction of a benzaldehyde tether with a cyclic enone |