Gold(i )-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans
Тип публикации: Journal Article
Дата публикации: 2020-07-03
scimago Q1
wos Q2
БС1
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
PubMed ID:
32657308
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
An unprecedented gold(I)-catalyzed cyclization of cyclopropylidene-tethered propargylic alcohols via a 6-endo-dig enyne cyclization followed by a ring-opening of cyclopropane and nucleophilic closure reaction to construct naphtho[2,3-c]pyrans was developed. This transformation represents a highly efficient method for the synthesis of polycyclic compounds in one-pot, and two new rings are formed in an atom economic manner.
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Li J. et al. Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans // Chemical Communications. 2020. Vol. 56. No. 64. pp. 9154-9157.
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Li J., Yang F., Hu W., Ren B., Chen Z., Ji K. Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans // Chemical Communications. 2020. Vol. 56. No. 64. pp. 9154-9157.
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TY - JOUR
DO - 10.1039/d0cc03285a
UR - https://xlink.rsc.org/?DOI=D0CC03285A
TI - Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans
T2 - Chemical Communications
AU - Li, Jian
AU - Yang, Fang
AU - Hu, Weiwei
AU - Ren, Bo
AU - Chen, Zisheng
AU - Ji, Kai-Da
PY - 2020
DA - 2020/07/03
PB - Royal Society of Chemistry (RSC)
SP - 9154-9157
IS - 64
VL - 56
PMID - 32657308
SN - 1359-7345
SN - 1364-548X
ER -
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@article{2020_Li,
author = {Jian Li and Fang Yang and Weiwei Hu and Bo Ren and Zisheng Chen and Kai-Da Ji},
title = {Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans},
journal = {Chemical Communications},
year = {2020},
volume = {56},
publisher = {Royal Society of Chemistry (RSC)},
month = {jul},
url = {https://xlink.rsc.org/?DOI=D0CC03285A},
number = {64},
pages = {9154--9157},
doi = {10.1039/d0cc03285a}
}
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Li, Jian, et al. “Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans.” Chemical Communications, vol. 56, no. 64, Jul. 2020, pp. 9154-9157. https://xlink.rsc.org/?DOI=D0CC03285A.