Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines.
about
Diversity through phosphine catalysis identifies octahydro-1,6-naphthyridin-4-ones as activators of endothelium-driven immunity.Diversity-oriented synthesis based on the DPPP-catalyzed mixed double-Michael reactions of electron-deficient acetylenes and β-amino alcohols.PHOSPHINE-CATALYZED [3 + 2] ANNULATION: SYNTHESIS OF ETHYL 5-(tert-BUTYL)-2-PHENYL-1-TOSYL-3-PYRROLINE-3-CARBOXYLATEPhosphine-catalyzed annulations of azomethine imines: allene-dependent [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] pathways.One-pot phosphine-catalyzed syntheses of quinolinesA torquoselective 6π electrocyclization approach to reserpine alkaloids.PHOSPHINE-CATALYZED [4+2] ANNULATION: SYNTHESIS OF ETHYL 6-PHENYL-1-TOSYL-1,2,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLATE.Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs.Asymmetric catalysis with chiral oxazolidine ligands.Stereoselective synthesis of substituted 1,3-oxazolidines via Pd-catalyzed carboamination reactions of O-vinyl-1,2-amino alcohols.Enantioselective intermolecular crossed-conjugate additions between nitroalkenes and alpha,beta-enals through a dual activation strategy.Phosphine-initiated general base catalysis: facile access to benzannulated 1,3-diheteroatom five-membered rings via double-Michael reactions of allenes.Diphosphine-catalyzed mixed double-Michael reaction: a unified synthesis of indolines, dihydropyrrolopyridines, benzimidazolines, tetrahydroquinolines, tetrahydroisoquinolines, dihydrobenzo-1,4-oxazines, and dihydrobenzo-3,1-oxazinesTheory-Guided Design of Brønsted Acid-Assisted Phosphine Catalysis: Synthesis of Dihydropyrones from Aldehydes and Allenoates.Stereoselective Syntheses of α,β-Unsaturated γ-Amino Esters Through Phosphine-Catalyzed γ-Umpolung Additions of Sulfonamides to γ-Substituted Allenoates.Synthesis of Functionalized Alkylidene Indanes and Indanones through Tandem Phosphine-Palladium CatalysisChiral aminophosphines as catalysts for enantioselective double-Michael indoline synthesesPhosphine/palladium-catalyzed syntheses of alkylidene phthalans, 3-deoxyisoochracinic acid, isoochracinic acid, and isoochracinol.Phosphine-catalyzed intramolecular γ-umpolung addition of α-aminoalkylallenic esters: facile synthesis of 3-carbethoxy-2-alkyl-3-pyrrolines.Alcohol-assisted phosphine catalysis: one-step syntheses of dihydropyrones from aldehydes and allenoates.Phosphine-Catalyzed Intramolecular Cyclizations of α-Nitroethylallenoates Forming (Z)-Furanone Oximes.Synthesis of 2-Alkynoates by Palladium(II)-Catalyzed Oxidative Carbonylation of Terminal Alkynes and Alcohols.Diastereoselective C-H Bond Amination for Disubstituted Pyrrolidines.Enantioselective [3+2] cycloaddition of azomethine ylides and aldehydes via Ni/bis(oxazoline)-catalyzed ring opening of N-tosylaziridines through a chirality transfer approach.Amino acid derived phosphine-catalyzed enantioselective 1,4-dipolar spiroannulation of cyclobutenones and isatylidenemalononitrile.Phosphine-catalyzed domino reaction: an efficient method for the synthesis of highly functionalized spirooxazolines.Chiral phosphine catalyzed asymmetric Michael addition of oxindoles.An asymmetric alkynylation/hydrothiolation cascade: an enantioselective synthesis of thiazolidine-2-imines from imines, acetylenes and isothiocyanates.Phosphine-initiated domino reaction: a convenient method for the preparation of spirocyclopentanones.
P2860
Q33839073-EFAD49C8-A9E5-4046-AA8F-07991C6E1B71Q34020882-C1D5E52C-3BA7-4E9D-A0DF-383F5EF85A26Q34637917-CE97DFDE-421F-4B73-8820-127706C67BDDQ35184786-280E24C4-97AA-43BD-9BEF-D2391AB8F60EQ36283901-AC803C66-26EC-4C01-BA30-52BCDC5FCFBCQ36368501-F96F3111-E968-4B20-89DF-75254392ECA6Q37271990-A9880D9C-356B-4332-88E4-0EDEE00C40E3Q37495686-49FD1766-1634-4CB9-81B9-C60DD8272F2CQ37829921-42DFCEE1-AD3E-465F-9DE6-F25823085864Q38266971-019E94B0-E862-4B3C-AD9E-BBF34A99316CQ38551335-B51C2407-FABB-49DD-A847-5063FD7037A6Q38708680-86840868-D4AB-4C14-AAE7-A013FDF73938Q39524260-CA3EAB92-7D17-4A8B-8D3E-B5CCDC56D118Q41115696-82C6BE48-5A3D-47CD-AF57-D5E16B77DBD2Q41453616-03624559-0CA1-4240-B861-4058E657C60FQ41476459-EA107674-449B-4CCE-9210-4CF4F8E7DD2AQ41823492-35D17FA1-DB5D-46ED-85DE-99E7DF5C9B03Q41966929-436D0BD9-7A6D-4D4F-978B-28F8BBA5B897Q42094790-9E1DA600-9E31-40AC-9724-C9DCF5E4142FQ42150888-20B98163-893A-4396-A952-00204F7D3230Q42173834-2EEEE6A4-F818-4CD8-A254-D289B759D036Q42316778-D503FDF7-B347-49FC-9FB2-29C43B5A031EQ48199130-AF4F2DD0-4F92-46B4-9440-A40A250FD09FQ50202231-F2DF1BB8-5552-427D-B5FB-47A369654C01Q50282439-2E4588E7-3AEF-47A8-A044-FF62B2928521Q52742039-B429E43A-E3B1-43F5-A95F-E888646AD1E5Q52747517-2AC02902-D5D0-47BB-971A-868A69DC6ED4Q53587876-6ECE0DE2-82F0-4573-8B22-2DDD152E5224Q53588027-57805202-6445-4FFB-A08A-31FD621C9C09
P2860
Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Bisphosphine-catalyzed mixed d ...... iazolidines, and pyrrolidines.
@en
type
label
Bisphosphine-catalyzed mixed d ...... iazolidines, and pyrrolidines.
@en
prefLabel
Bisphosphine-catalyzed mixed d ...... iazolidines, and pyrrolidines.
@en
P2093
P2860
P356
P1476
Bisphosphine-catalyzed mixed d ...... iazolidines, and pyrrolidines.
@en
P2093
Gregg A Barcan
Ohyun Kwon
Vardhineedi Sriramurthy
P2860
P304
12928-12929
P356
10.1021/JA073754N
P407
P577
2007-10-09T00:00:00Z