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Aryl Hydrazide beyond as Surrogate of Aryl Hydrazine in the Fischer Indolization: The Synthesis of N-Cbz-indoles, N-Cbz-carbazoles, and N,N '-Bis-Cbz-pyrrolo[2,3-f]indoles
- Issue Date
- Dec-2009
- Publisher
- AMER CHEMICAL SOC
- Citation
- ORGANIC LETTERS, v.11, no.23, pp.5454 - 5456
- Indexed
- SCIE
SCOPUS
- Journal Title
- ORGANIC LETTERS
- Volume
- 11
- Number
- 23
- Start Page
- 5454
- End Page
- 5456
- ISSN
- 1523-7060
- Abstract
- Aryl hydrazides underwent the Fischer indolization reactions, while the N-carbamate group(s) remained intact to directly provide N-Cbz-indoles. This new method allowed the synthesis of various N-Cbz-carbazoles and N,N'-bis-Cbz-pyrrolo[2,3-f]indoles.
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Related Researcher
- Cho, Cheon Gyu
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)