Ring opening of donor-acceptor-type cyclopropene unveils electrophilic ketene with vinylogous [4 C + n] periselective cyclization mode
Abstract Since its advent 120 years ago, the [2+n] coupling cyclization of ketene has been prevalently used for the synthesis of N- and O-heterocycles. In contrast, its vinylogous version, i.e., use of alkenyl ketene as 4 C synthon, remain elusive. We report herein that in the rare SN1-type ring-ope...
Saved in:
| Main Authors: | Jianhong Huang, Jiahang Li, Shenli Liu, Wanyao Zhao, Yan Xia, Xiaoyan Liu, Kuizhan Shao, Wenliang Li, Haiyan Yuan, Jinbo Zhao |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-04-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-59048-y |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Stereochemistry of the Diels-Alder Addition of Halogenated Cyclopropenes
by: Paul Müller, et al.
Published: (1987-08-01) -
Vinylogous functionalization of 4-alkylidene-5-aminopyrazoles with methyl trifluoropyruvates
by: Judit Hostalet-Romero, et al.
Published: (2025-03-01) -
REACTION OF QUINONEIMINES WITH
KETENES
Published: (1994-06-01) -
Zur Chemie der Ketene
by: E. Ziegler
Published: (1970-02-01) -
Enantioselective aza-electrophilic dearomatization of naphthalene derivatives
by: Jun Liu, et al.
Published: (2025-07-01)