Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

about

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

Item

http://www.wikidata.org/entity/Q48123177

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@en

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@nl

type

Item

label

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@en

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@nl

prefLabel

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@en

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines.

@nl

P1476

Alkenyl Isocyanide Conjugate Additions: A Rapid Route to γ-Carbolines

@en

P2093

Allen Chao

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

Sergiy V Chepyshev

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

P2860

Exposing the hidden complexity of stoichiometric and catalytic metathesis reactions by elucidation of Mg-Zn hybrids.

Recent developments in isocyanide based multicomponent reactions in applied chemistry.

Catalytic Isonitrile Insertions and Condensations Initiated by RNC-X Complexation

Marine isocyanides and related natural products--structure, biosynthesis and ecology.

Beyond thermodynamic acidity: a perspective on the complex-induced proximity effect (CIPE) in deprotonation reactions.

Alkyl Sulfinates: Formal Nucleophiles for Synthesizing TosMIC Analogs.

Synthesis of marine natural products with antimalarial activity.

Evolving organic synthesis fostered by the pluripotent phenylsulfone moiety.

Recent advances in the synthesis of nitrogen heterocycles via radical cascade reactions using isonitriles as radical acceptors.

Ingenines A and B, Two New Alkaloids from the Indonesian Sponge Acanthostrongylophora ingens.

P304

4310-4313

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

P31

scholarly article

P356

10.1002/ANIE.201612574

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

P407

English

P433

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

P478

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

P50

Fraser Fleming

Armando Lujan-Montelongo

P577

2017-03-13T00:00:00Z

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

P698

28295938

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

P932

5667947

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