Journal
ORGANIC LETTERS
Volume 11, Issue 23, Pages 5454-5456Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol902250x
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Funding
- Korea Science and Engineering Foundation through Center for Bioactive Molecular Hybrids (CBMH), Yonsei University
- BK21 Fellowship
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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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