Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative
Yao Xiao
1
,
Xin Peng
1
,
Jie Shen
1
,
Lei Cui
1
,
Shanya Lu
1
,
Xueshun Jia
1
,
Chunju Li
2
,
Jian Li
1, 3
Publication type: Journal Article
Publication date: 2022-08-25
scimago Q1
wos Q2
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
36043872
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Abstract
A series of structurally unusual spirobenzoxazine chromeno[4,3-b]pyrrole derivatives have been efficiently constructed in a single operation from readily available starting materials. This domino transformation forms successively three new rings and provides a fast and economic strategy with excellent diastereoselectivity.
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Metrics
13
Total citations:
13
Citations from 2025:
6
(46.15%)
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GOST
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Xiao Y. et al. Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative // Chemical Communications. 2022. Vol. 58. No. 75. pp. 10528-10531.
GOST all authors (up to 50)
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Xiao Y., Peng X., Shen J., Cui L., Lu S., Jia X., Li C., Li J. Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative // Chemical Communications. 2022. Vol. 58. No. 75. pp. 10528-10531.
Cite this
RIS
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TY - JOUR
DO - 10.1039/d2cc02454c
UR - https://xlink.rsc.org/?DOI=D2CC02454C
TI - Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative
T2 - Chemical Communications
AU - Xiao, Yao
AU - Peng, Xin
AU - Shen, Jie
AU - Cui, Lei
AU - Lu, Shanya
AU - Jia, Xueshun
AU - Li, Chunju
AU - Li, Jian
PY - 2022
DA - 2022/08/25
PB - Royal Society of Chemistry (RSC)
SP - 10528-10531
IS - 75
VL - 58
PMID - 36043872
SN - 1359-7345
SN - 1364-548X
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2022_Xiao,
author = {Yao Xiao and Xin Peng and Jie Shen and Lei Cui and Shanya Lu and Xueshun Jia and Chunju Li and Jian Li},
title = {Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative},
journal = {Chemical Communications},
year = {2022},
volume = {58},
publisher = {Royal Society of Chemistry (RSC)},
month = {aug},
url = {https://xlink.rsc.org/?DOI=D2CC02454C},
number = {75},
pages = {10528--10531},
doi = {10.1039/d2cc02454c}
}
Cite this
MLA
Copy
Xiao, Yao, et al. “Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative.” Chemical Communications, vol. 58, no. 75, Aug. 2022, pp. 10528-10531. https://xlink.rsc.org/?DOI=D2CC02454C.