P(NMe2)3-Mediated Umpolung Spirocyclopropanation Reaction of p-Quinone Methides: Diastereoselective Synthesis of Spirocyclopropane-Cyclohexadienones

YH Deng, WD Chu, YH Shang, KY Yu, ZL Jia… - Organic …, 2020 - ACS Publications
An unprecedented umpolung spirocyclopropanation reaction of p-quinone methides and α-
keto carbonyls is described. Our umpolung strategy based on 1, 6-conjugate addition and …

Tandem Spirocyclopropanation/Rearrangement Reaction of Vinyl p-Quinone Methides with Sulfonium Salts: Synthesis of Spirocyclopentenyl p-Dienones

XZ Zhang, YH Deng, KJ Gan, X Yan, KY Yu… - Organic …, 2017 - ACS Publications
A novel base-mediated tandem spirocyclopropanation/rearrangement reaction of vinyl p-
quinone methides (p-VQMs) with sulfonium salts is described. The unprecedented reactivity …

Spirocyclopropanation Reaction of para-Quinone Methides with Sulfonium Salts: The Synthesis of Spirocyclopropanyl para-Dienones

XZ Zhang, JY Du, YH Deng, WD Chu… - The Journal of …, 2016 - ACS Publications
A novel DBU-mediated stereoselective spirocyclopropanation of para-quinone methides
with sulfonium salts has been developed on the basis of the mode involving a 1, 6-conjugate …

PIII-Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles

J Zhang, J Hao, Z Huang, J Han, Z He - Chemical Communications, 2020 - pubs.rsc.org
AP (NMe2) 3-mediated reductive intramolecular cyclopropanation is developed for the first
time, which provides facile access to a wide variety of cyclopropane-fused heterocycles …

Unusual Formal [1+4] Annulation through Tandem P(NMe2)3‐Mediated Cyclopropanation/Base‐Catalyzed Cyclopropane Rearrangement: Facile Syntheses of …

R Zhou, K Zhang, L Han, Y Chen… - Chemistry–A European …, 2016 - Wiley Online Library
Abstract An unusual formal [1+ 4] annulation of α‐dicarbonyl compounds with 1, 1‐dicyano‐
1, 3‐dienes has been realized, leading to facile syntheses of cyclopentenimines and …

Diastereoselective Syntheses of Chroman Spiroketals via [4 + 2] Cycloaddition of Enol Ethers and o-Quinone Methides

MA Marsini, Y Huang, CC Lindsey, KL Wu… - Organic …, 2008 - ACS Publications
A variety of chroman spiroketals are synthesized via inverse-demand [4+ 2] cycloaddition of
enol ethers and ortho-quinone methides (o-QMs). Low temperature o-QM generation in situ …

Diastereoselective Synthesis of Functionalized Spirocyclopropyl Oxindoles via P(NMe2)3-Mediated Reductive Cyclopropanation

R Zhou, C Yang, Y Liu, R Li, Z He - The Journal of Organic …, 2014 - ACS Publications
AP (NMe2) 3-mediated reductive cyclopropanation reaction of α-keto esters or amides with
isatin-derived alkenes has been developed, providing efficient and diastereoselective …

Asymmetric total syntheses of (−)-penicipyrone and (−)-tenuipyrone via biomimetic cascade intermolecular Michael addition/cycloketalization

L Song, H Yao, L Zhu, R Tong - Organic letters, 2013 - ACS Publications
The first total syntheses of (−)-penicipyrone and (−)-tenuipyrone were accomplished
enantioselectively in 12 steps with an 11% yield and 6 steps with a 28% yield from the …

Stereoselective 1,6-Conjugate Addition/Annulation of para-Quinone Methides with Vinyl Epoxides/Cyclopropanes

C Ma, Y Huang, Y Zhao - ACS Catalysis, 2016 - ACS Publications
Here, we present an unprecedented formal [3+ 2] cycloaddition of para-quinone methides
with vinyl epoxides/cyclopropanes to deliver a wide range of spiro [4.5] decanes in high …

[HTML][HTML] Synthesis of bicyclo [3.1. 0] hexanes by (3+ 2) annulation of cyclopropenes with aminocyclopropanes

B Muriel, A Gagnebin, J Waser - Chemical science, 2019 - pubs.rsc.org
We report the convergent synthesis of bicyclo [3.1. 0] hexanes possessing an all-carbon
quaternary center via a (3+ 2) annulation of cyclopropenes with cyclopropylanilines. Using …