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1.
Chem Commun (Camb) ; 55(71): 10567-10570, 2019 Aug 29.
Article in English | MEDLINE | ID: mdl-31417998

ABSTRACT

Macrocyclization of linear peptide precursors using the Petasis borono-Mannich reaction affords a diverse range of macrocycles with an endocyclic amine. Analysis of the corresponding macrocyclic structures underscores that the hydrogen bond between an endocyclic amine and the adjacent amide NH is a powerful control element for conformationally homogenous peptide macrocycles.


Subject(s)
Boronic Acids/chemistry , Macrocyclic Compounds/chemical synthesis , Peptides, Cyclic/chemical synthesis , Aldehydes/chemistry , Amides/chemistry , Amines/chemistry , Aziridines/chemistry , Cyclization
2.
Molecules ; 17(2): 1617-34, 2012 Feb 07.
Article in English | MEDLINE | ID: mdl-22314382

ABSTRACT

Catalytic asymmetric Corey-Chaykovsky epoxidation of various ketones with dimethyloxosulfonium methylide using a heterobimetallic La-Li(3)-BINOL complex (LLB) is described. The reaction proceeded smoothly at room temperature in the presence of achiral phosphine oxide additives, and 2,2-disubstituted terminal epoxides were obtained in high enantioselectivity (97%-91% ee) and yield ( > 99%-88%) from a broad range of methyl ketones with 1-5 mol% catalyst loading. Enantioselectivity was strongly dependent on the steric hindrance, and other ketones, such as ethyl ketones and propyl ketones resulted in slightly lower enantioselectivity (88%-67% ee).


Subject(s)
Epoxy Compounds/chemistry , Ketones/chemistry , Catalysis , Magnetic Resonance Spectroscopy , Spectrometry, Mass, Electrospray Ionization , Spectroscopy, Fourier Transform Infrared , Stereoisomerism
3.
J Am Chem Soc ; 131(31): 10842-3, 2009 Aug 12.
Article in English | MEDLINE | ID: mdl-19722664

ABSTRACT

A Ba-catalyzed dynamic kinetic asymmetric transformation (DYKAT) involving a direct aldol/retro-aldol reaction of beta,gamma-unsaturated ester donors is described. A Ba(O-iPr)(2)/BINOL complex promoted the direct aldol reaction/isomerization sequence, and alpha-alkylidene-beta-hydroxy esters were obtained from aryl, heteroaryl, alkenyl, and alkyl aldehydes under simple proton-transfer conditions with 99-87% ee and >20:1 to 15:1 alpha/gamma selectivity.


Subject(s)
Aldehydes/chemistry , Barium/chemistry , Esters/chemical synthesis , Catalysis , Isomerism , Kinetics
4.
J Am Chem Soc ; 130(31): 10078-9, 2008 Aug 06.
Article in English | MEDLINE | ID: mdl-18613663

ABSTRACT

Catalytic asymmetric Corey-Chaykovsky epoxidation of ketones with dimethyloxosulfonium methylide 2 using an LLB 1a + Ar3P O complex proceeded smoothly at room temperature, and 2,2-disubstituted terminal epoxides were obtained in high enantioselectivity (91-97%) and yield (>88-99%) from a broad range of methyl ketones with 1-5 mol % catalyst loading. The use of achiral additive Ar3P O 5i was important to achieve high enantioselectivity.


Subject(s)
Epoxy Compounds/chemical synthesis , Ketones/chemistry , Sulfonium Compounds/chemistry , Catalysis , Organophosphorus Compounds
5.
Org Lett ; 10(11): 2319-22, 2008 Jun 05.
Article in English | MEDLINE | ID: mdl-18459795

ABSTRACT

Direct catalytic asymmetric Mannich-type reactions of gamma-butenolides are described. A chiral Lewis acid/amine base/Brønsted acid combination was used to catalyze a gamma-addition of gamma-butenolides to N-diphenylphosphinoyl imines, affording the products in up to >99% yield, anti/syn = >97:3, and 84% ee. The use of a catalytic amount of TfOH in addition to La(OTf)3/Me-PyBox/TMEDA was important for improving yield and stereoselectivity.


Subject(s)
4-Butyrolactone/analogs & derivatives , Metals/chemistry , 4-Butyrolactone/chemistry , Acids/chemistry , Catalysis , Imines/chemistry , Mannich Bases/chemistry , Stereoisomerism , Substrate Specificity
6.
Org Lett ; 9(17): 3387-90, 2007 Aug 16.
Article in English | MEDLINE | ID: mdl-17655253

ABSTRACT

Barium-catalyzed direct Mannich-type reactions of a beta,gamma-unsaturated ester are described. The Ba-catalyst not only promoted the Mannich-type reactions, but also isomerized Mannich adducts to afford beta-methyl aza-Morita-Baylis-Hillman-type products in 61-88% yield from various aryl, heteroaryl, and alkyl imines. Preliminary trials on enantioselective variants with a chiral biaryldiol ligand gave products in up to 80% ee.


Subject(s)
Barium/chemistry , Esters/chemistry , Alkenes/chemistry , Catalysis , Ligands
8.
Org Lett ; 7(23): 5339-42, 2005 Nov 10.
Article in English | MEDLINE | ID: mdl-16268573

ABSTRACT

[reaction, structure: see text] Chiral Y{N(SiMe3)2}3/linked-BINOL catalyst generated Y-enolate in situ from various hydroxyketones (R2 = aryl, heteroaryl). Beta-amino-alpha-hydroxy ketones (R1 = aryl, heteroaryl, alkenyl) were obtained syn-selectively (up to 96/4) in high ee (up to 98%) and good yield (up to 98% yield).

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