An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy
Publication
, Journal Article
Zhou, B; Liu, Z-C; Qu, W-W; Yang, R; Lin, X-R; Yan, S-J; Lin, J
Published in: Green Chem.
2014
The first site-selective methodology for the construction of fused [1,2-]indolone derivativesan unexpected anti-Nenitzescu strategy has been developed.
Duke Scholars
Published In
Green Chem.
DOI
EISSN
1463-9270
ISSN
1463-9262
Publication Date
2014
Volume
16
Issue
9
Start / End Page
4359 / 4370
Publisher
Royal Society of Chemistry (RSC)
Related Subject Headings
- Organic Chemistry
- 34 Chemical sciences
- 03 Chemical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Zhou, B., Liu, Z.-C., Qu, W.-W., Yang, R., Lin, X.-R., Yan, S.-J., & Lin, J. (2014). An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy. Green Chem., 16(9), 4359–4370. https://doi.org/10.1039/c4gc00676c
Zhou, Bei, Zhi-Cheng Liu, Wen-Wen Qu, Rui Yang, Xin-Rong Lin, Sheng-Jiao Yan, and Jun Lin. “An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy.” Green Chem. 16, no. 9 (2014): 4359–70. https://doi.org/10.1039/c4gc00676c.
Zhou B, Liu Z-C, Qu W-W, Yang R, Lin X-R, Yan S-J, et al. An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy. Green Chem. 2014;16(9):4359–70.
Zhou, Bei, et al. “An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy.” Green Chem., vol. 16, no. 9, Royal Society of Chemistry (RSC), 2014, pp. 4359–70. Crossref, doi:10.1039/c4gc00676c.
Zhou B, Liu Z-C, Qu W-W, Yang R, Lin X-R, Yan S-J, Lin J. An environmentally benign, mild, and catalyst-free reaction of quinones with heterocyclic ketene aminals in ethanol: site-selective synthesis of rarely fused [1,2-a]indolone derivatives via an unexpected anti-Nenitzescu strategy. Green Chem. Royal Society of Chemistry (RSC); 2014;16(9):4359–4370.
Published In
Green Chem.
DOI
EISSN
1463-9270
ISSN
1463-9262
Publication Date
2014
Volume
16
Issue
9
Start / End Page
4359 / 4370
Publisher
Royal Society of Chemistry (RSC)
Related Subject Headings
- Organic Chemistry
- 34 Chemical sciences
- 03 Chemical Sciences