Ortho-Hydroxylative ipso-Cyclization of N-arylpropiolamide

YC Wang, JB Liu, H Zhou, W Xie… - The Journal of …, 2019 - ACS Publications
A facile protocol for the tunable synthesis of 10-hydroxy-1-azaspiro [4.5] deca-3, 6, 8-trien-2-
ones and benzo [b] pyrrolo [2, 1-c][1, 4] oxazin-3-ones is described. A tunable synthesis has …

Radical bromination-induced ipso cyclization–ortho cyclization sequence of N-hydroxylethyl-N-arylpropiolamides

YC Wang, K Huang, X Lai, Z Shi, JB Liu… - Organic & Biomolecular …, 2021 - pubs.rsc.org
A facile procedure is reported for the synthesis of various 2-bromo-1-phenyl-5, 6-dihydro-3H,
7aH-benzo [b] pyrrolo [2, 1-c][1, 4] oxazin-3-ones via a radical bromination-induced ipso …

ZnBr 2/Oxone-mediated ipso-cyclization of N-(3-phenylprop-2-yn-1-yl) aniline

K Huang, JN Li, G Qiu, W Xie, JB Liu - RSC advances, 2019 - pubs.rsc.org
In this work, a selective synthetic strategy towards 1-azaspiro [4.5] deca-3, 6, 9-trien-8-ones
from N-tosyl-N-(prop-2-yn-1-yl) aniline is developed. The transformation proceeds smoothly …

Metal-free spirocyclization of N-arylpropiolamides with glyoxylic acids: access to complex azaspiro-fused tricycles

AM Nair, AH Shinde, S Kumar… - Chemical Communications, 2020 - pubs.rsc.org
A metal-free oxidative cascade acylation and dearomatization of N-(p-methoxyaryl)
propiolamides was achieved via K2S2O8 mediated decarboxylation of α-oxocarboxylic …

Switchable Regioselective 7-endo or 6-exo Iodocyclization of O-Homoallyl Benzimidates

TY Cao, L Qi, LJ Wang - The Journal of Organic Chemistry, 2023 - ACS Publications
We present a facile switchable regioselective 7-endo or 6-exo iodocyclization of O-homoallyl
benzimidates here, which affords various iodo-substituted 1, 3-oxazines and tetrahydro-1, 3 …

Spirooxazoline synthesis by an oxidative dearomatizing cyclization

MU Tariq, WJ Moran - European Journal of Organic Chemistry, 2020 - Wiley Online Library
Spirocyclic compounds are of increasing importance owing to their potential applications in
the development of new pharmaceuticals. Herein, we describe a new, rapid access to rarely …

Mild synthesis of isoxazoline derivatives via an efficient [4+ 1] annulation reaction of transient nitrosoalkenes and sulfur ylides

TB Hua, CX Liu, WM Hu, L Wang, QQ Yang - Scientific Reports, 2021 - nature.com
Abstract An efficient [4+ 1] annulation between α-bromooximes and sulfur ylides via in situ
generation of nitrosoalkenes under mild basic reaction conditions has been developed …

[3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted …

YA Antonova, YV Nelyubina, SL Ioffe, AA Tabolin - Molecules, 2023 - mdpi.com
A rhodium (II)-catalyzed reaction of cyclic nitronates (5, 6-dihydro-4 H-1, 2-oxazine N-
oxides) with vinyl diazoacetates proceeds as a [3+ 3]-annulation producing bicyclic …

ZnBr 2-Mediated oxidative spiro-bromocyclization of propiolamide for the synthesis of 3-bromo-1-azaspiro [4.5] deca-3, 6, 9-triene-2, 8-dione

Y He, G Qiu - Organic & Biomolecular Chemistry, 2017 - pubs.rsc.org
ZnBr2-Mediated oxidative spiro-bromocyclization of N-arylpropiolamide has been described
herein for the synthesis of 3-bromo-1-azaspiro [4.5] deca-3, 6, 9-triene-2, 8-dione with high …

A One-Pot Synthesis of Pyrido[2,3-b][1,4]oxazin-2-ones

SD Cho, YD Park, JJ Kim, SG Lee, C Ma… - The Journal of …, 2003 - ACS Publications
Pyrido [2, 3-b][1, 4] oxazin-2-ones are conveniently prepared in excellent yields by a one-pot
annulation of N-substituted-2-chloroacetamides with 2-halo-3-hydroxypyridines with use of …