SCOPUS 정보 검색 플랫폼

Tetrahedron

Volumn 70, Issue 3, 2014, Pages 702-707

Gold(I)-catalyzed rearrangement of alkynylaziridine indoles for the synthesis of spiro-tetrahydro-β-carbolines

(5) Yang, Yan Fang a Li, Lian Hua a He, Yu Tao a Luo, Jian Yi a Liang, Yong Min a,b

a LANZHOU UNIVERSITY (China)

b LANZHOU INSTITUTE OF CHEMICAL PHYSICS (China)

Author keywords

Aminoallene; Cyclization; Gold; Rearrangement; Tetrahydro carboline

Indexed keywords

AZIRIDINE; BETA CARBOLINE DERIVATIVE; DICHLOROMETHANE; GOLD; INDOLE DERIVATIVE; SILVER; SPIRO COMPOUND;

AROMATIZATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; COLUMN CHROMATOGRAPHY; CYCLIZATION; FRIEDEL CRAFTS REACTION; MITSUNOBU REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; PROTON TRANSPORT; REACTION ANALYSIS; ROOM TEMPERATURE; SOLVENT EFFECT; STEREOSPECIFICITY; SYNTHESIS; THIN LAYER CHROMATOGRAPHY; X RAY DIFFRACTION;

EID: 84892948301 PISSN: 00404020 EISSN: 14645416 Source Type: Journal
DOI: 10.1016/j.tet.2013.11.084 Document Type: Article

Times cited : (15)

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- There was no reaction below 50 C, this process need more energy than one-pot reaction.

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