Rearrangements of Furan-, Thiophene- andN-Boc-Pyrrole-Derived Donor-Acceptor Cyclopropanes: Scope and Limitations
出版年份 2013 全文链接
标题
Rearrangements of Furan-, Thiophene- andN-Boc-Pyrrole-Derived Donor-Acceptor Cyclopropanes: Scope and Limitations
作者
关键词
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出版物
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2013, Issue 21, Pages 4539-4551
出版商
Wiley
发表日期
2013-06-07
DOI
10.1002/ejoc.201300390
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- (2013) Johannes Kaschel et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
- (2012) Yaojia Jiang et al. CHEMICAL COMMUNICATIONS
- Donor–acceptor cyclopropanes with Lawesson's and Woollins' reagents: formation of bisthiophenes and unprecedented cage-like molecules
- (2012) Johannes Kaschel et al. CHEMICAL COMMUNICATIONS
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- (2012) Huina Wang et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- ShelXle: a Qt graphical user interface forSHELXL
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- Stereoselective synthesis and applications of nitrogen substituted donor–acceptor cyclopropanes (N-DACs) in the divergent synthesis of azacycles
- (2011) Santosh J. Gharpure et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Ring-Enlargement Reactions of Donor−Acceptor-Substituted Cyclopropanes: Which Combinations are Most Efficient?
- (2011) Tobias F. Schneider et al. ORGANIC LETTERS
- Iron-Catalyzed [3 + 2] Annulation of Aminocyclopropanes with Aldehydes: Stereoselective Synthesis of Aminotetrahydrofurans
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- From Furan to Molecular Stairs: Syntheses, Structural Properties, and Theoretical Investigations of Oligocyclic Oligoacetals
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- (2010) Mahmoud M. Abd Rabo Moustafa et al. ORGANIC LETTERS
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