Alkylation/Ipso-cyclization of Active Alkynes Leading to 3-Alkylated Aza-and Oxa-spiro [4, 5]-trienones

P Chen, JH Fan, WQ Yu, BQ Xiong, Y Liu… - The Journal of …, 2022 - ACS Publications
A method for the preparation of 3-alkylated spiro [4.5] trienones via alkylation/ipso-
cyclization of activated alkynes with 4-alkyl-DHPs under transition-metal-free conditions is …

Intramolecular ipso-Halocyclization of 4-(p-Unsubstituted-aryl)-1-alkynes Leading to Spiro[4,5]trienones: Scope, Application, and Mechanistic Investigations

BX Tang, YH Zhang, RJ Song, DJ Tang… - The Journal of …, 2012 - ACS Publications
A new, general method for the synthesis of spiro [4, 5] trienones is described by the
intramolecular ipso-halocyclization of 4-(p-unsubstituted-aryl)-1-alkynes. In the presence of …

Visible‐Light‐Mediated Nitrogen‐Centered Radical Strategy: Preparation of 3‐Acylated Spiro [4, 5] trienones

P Chen, J Xie, Z Chen, BQ Xiong, Y Liu… - Advanced Synthesis …, 2021 - Wiley Online Library
A nitrogen‐centered radical strategy for the preparation of 3‐acylated spiro [4, 5] trienones
via visible‐light‐mediated acylation/ipso‐cyclization of alkynes with acyl oxime esters is …

Halogen-Radical-Promoted Dearomative Aza-Spirocyclization of Alkynylimines: An Efficient Approach to 3-Halo-Spirocyclohexadienones

D Chen, J Li, Y Shan, P Cui, Y Zhao, L Tian, G Qiu - Synthesis, 2020 - thieme-connect.com
A novel halogen-radical-promoted dearomative aza-spirocyclization of alkynylimines for the
synthesis of 3-halo-spirocyclohexadienones is described. In this process, it is believed that a …

Metal-free oxidative spirocyclization of alkynes with sulfonylhydrazides leading to 3-sulfonated azaspiro [4, 5] trienones

J Wen, W Wei, S Xue, D Yang, Y Lou… - The Journal of …, 2015 - ACS Publications
A novel and direct oxidative spirocyclization of arylpropiolamides with sulfonylhydrazides
leading to 3-sulfonated azaspiro [4, 5] trienones has been developed under metal-free …

Selective Synthesis of Spiro[4,5]trienyl Acetates via an Intramolecular Electrophilic ipso-Iodocyclization Process

BX Tang, DJ Tang, S Tang, QF Yu, YH Zhang… - Organic …, 2008 - ACS Publications
A general and efficient intramolecular electrophilic ipso-iodocyclization of para-unactivated
arylalkynes has been developed for the synthesis of spiro [4, 5] trienyl acetates. In the …

DTBP‐Mediated Cascade Spirocyclization and Dearomatization of Biaryl Ynones: Facile Access to Spiro[5.5]trienones through C(sp3)−H Bond Functionalization

MM Zhang, LY Shen, S Dong, B Li… - European Journal of …, 2021 - Wiley Online Library
DTBP‐Mediated Cascade Spirocyclization and Dearomatization of Biaryl Ynones: Facile Access
to Spiro[5.5]trienones through C(sp3)−H Bond Functionalization - Zhang - 2021 - European …

Electrochemical Dearomatizing Spirocyclization of Alkynes with D imethyl 2-Benzylmalonate s to Spiro [4.5] deca-trienones

L Li, ZW Hou, P Li, L Wang - The Journal of Organic Chemistry, 2022 - ACS Publications
An electrochemical dearomatizing spirocyclization of alkynes with dimethyl 2-
benzylmalonates for the preparation of spiro [4.5] deca-trienones has been developed. This …

Electrophilic Cyclization of 2-(1-Alkynyl)-2-alken-1-ones Using the I2/K3PO4 System:  An Efficient Synthesis of Highly Substituted Iodofurans

Y Liu, S Zhou - Organic Letters, 2005 - ACS Publications
The electrophilic cyclization of 2-(1-alkynyl)-2-alken-1-ones in the presence of various
alcohols or carbon-based nucleophiles offers an efficient and straightforward route to highly …

Substituent Effects in Samarium Diiodide-Induced 6-trig Cyclizations of γ-Arylketones to Functionalized Hexahydronaphthalene Derivatives

M Berndt, HU Reissig - Synlett, 2001 - thieme-connect.com
The samarium diiodide-induced 6-trig cyclizations of substituted g-arylketones 1, 4, 5, 9, 11,
and 14 are strongly influenced by substituents of the aryl group. Whereas para-methoxy …