Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base.

about

Synthesis of Enantioenriched Allylic Silanes via Nickel-Catalyzed Reductive Cross-Coupling.Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction.

P2860

Q47286675-F60501B3-38B0-44A3-B9A5-2757AFFF291C Q48056382-38BBAE03-9001-410F-8DF5-80364BBDFBA4

P2860

Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base.

Item

http://www.wikidata.org/entity/Q55075717

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh

2016年學術文章

@zh-hant

name

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@en

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@nl

type

Item

label

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@en

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@nl

prefLabel

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@en

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@nl

P1476

Enantioselective Aza-Sakurai C ...... s H-Bond Donor and Lewis Base.

@en

P2093

Corinna S Schindler

http://www.w3.org/2001/XMLSchema#string

Eric N Jacobsen

http://www.w3.org/2001/XMLSchema#string

Yongho Park

http://www.w3.org/2001/XMLSchema#string

P2860

Enantioselective thiourea-catalyzed cationic polycyclizations

Enantioselective Rhodium-Catalyzed [2 + 2 + 2] Cycloadditions of Terminal Alkynes and Alkenyl Isocyanates: Mechanistic Insights Lead to a Unified Model that Rationalizes Product Selectivity

A convergent stereoselective synthesis of quinolizidines and indolizidines: chemoselective coupling of 2-hydroxymethyl-substituted allylic silanes with imines.

Synthesis of amino acid derived enaminones via Wolff rearrangement using vinylogous amides as carbon nucleophiles

Lewis base catalysis of bromo- and iodolactonization, and cycloetherification

Thiourea-catalyzed enantioselective addition of indoles to pyrones: alkaloid cores with quaternary carbons.

Organometallic enantiomeric scaffolding: a strategy for the enantiocontrolled construction of regio- and stereodivergent trisubstituted piperidines from a common precursor

Synthesis of alkaloid (-)-205B via stereoselective reductive cross-coupling and intramolecular [3+2] cycloaddition.

Catalytic, asymmetric halofunctionalization of alkenes--a critical perspective.

Asymmetric organocatalytic cyclization and cycloaddition reactions.

P304

14848-14851

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1021/JACS.6B09736

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

138

http://www.w3.org/2001/XMLSchema#string

P577

2016-11-03T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27787993

http://www.w3.org/2001/XMLSchema#string

P921

enantioselectivity

P932

5148636

http://www.w3.org/2001/XMLSchema#string

Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base.

about

P2860

P2860

Enantioselective Aza-Sakurai Cyclizations: Dual Role of Thiourea as H-Bond Donor and Lewis Base.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932