Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels–Alder reaction versus aryne-mediated domino process

Dmitry S. Kopchuk; Igor L. Nikonov; Albert F. Khasanov; Kousik Giri; Sougata Santra; Igor S. Kovalev; Emiliya V. Nosova; Sravya Gundala; Padmavathi Venkatapuram; Grigory V. Zyryanov; Adinath Majee; Oleg N. Chupakhin

doi:10.1039/c8ob00847g

Studies on the interactions of 5-R-3-(2-pyridyl)-1,2,4-triazines with arynes: inverse demand aza-Diels–Alder reaction versus aryne-mediated domino process

Organic & Biomolecular Chemistry ◽

10.1039/c8ob00847g ◽

2018 ◽

Vol 16 (28) ◽

pp. 5119-5135 ◽

Cited By ~ 21

Author(s):

Dmitry S. Kopchuk ◽

Igor L. Nikonov ◽

Albert F. Khasanov ◽

Kousik Giri ◽

Sougata Santra ◽

...

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Inverse Demand

The interactions between substituted 5-R-3-(pyridyl-2)-1,2,4-triazines with in situ generated substituted aryne intermediates have been studied.

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Hetero-Diels—Alder Reaction of N-Cyanoaniline and Pyridinium Cyano(ethoxycarbonyl)methylide with Aroylketenes Generated in situ in Thermolysis of 6-Aryl-2,2-dimethyl-1,3-dioxin-4-ones.

ChemInform ◽

10.1002/chin.200705162 ◽

2007 ◽

Vol 38 (5) ◽

Author(s):

D. D. Nekrasov ◽

A. S. Obukhova

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction

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Organocatalytic enantioselective Diels–Alder reaction between hydroxymaleimides and in situ generated nitrosoalkenes for direct preparation of chiral hemiketals with 1,2-oxazine skeleton

Organic Chemistry Frontiers ◽

10.1039/d1qo01022k ◽

2021 ◽

Author(s):

Min Xiang ◽

Chen-Yi Li ◽

Jian Zhang ◽

Ying Zou ◽

Wen-Sheng Li ◽

...

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Direct Preparation

Organocatalytic Enantioselective IEDDA reaction between hydroxymaleimides and in situ generated nitrosoalkenes has been disclosed, a series of chiral hemiketals containing 5,6-dihydro-4H-l,2-oxazines and succinimide frameworks have been prepared.

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ChemInform Abstract: DIELS-ALDER REACTION OF HETEROCYCLIC AZADIENES. 2. “CATALYTIC” DIELS-ALDER REACTION OF IN SITU GENERATED ENAMINES WITH 1,2,4-TRIAZINES: GENERAL PYRIDINE ANNULATION

Chemischer Informationsdienst ◽

10.1002/chin.198228068 ◽

1982 ◽

Vol 13 (28) ◽

Author(s):

D. L. BOGER ◽

J. S. PANEK ◽

M. M. MEIER

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction

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Organocatalytic Asymmetric Hetero-Diels–Alder Reaction of in Situ Generated Dienes: Access to α,β-Unsaturated δ-Lactones Featuring CF3-Substituted Quaternary Stereocenter

The Journal of Organic Chemistry ◽

10.1021/acs.joc.9b03076 ◽

2020 ◽

Vol 85 (5) ◽

pp. 3202-3212

Author(s):

Harshit Joshi ◽

Ankit Yadav ◽

Arko Das ◽

Vinod K. Singh

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Quaternary Stereocenter

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In-situ forming thermosensitive hydroxypropyl chitin-based hydrogel crosslinked by Diels-Alder reaction for three dimensional cell culture

Carbohydrate Polymers ◽

10.1016/j.carbpol.2019.02.058 ◽

2019 ◽

Vol 212 ◽

pp. 368-377 ◽

Cited By ~ 15

Author(s):

Bo Bi ◽

Mengsi Ma ◽

Siyao Lv ◽

Renxi Zhuo ◽

Xulin Jiang

Keyword(s):

Cell Culture ◽

Three Dimensional ◽

Alder Reaction ◽

Diels Alder ◽

In Situ Forming ◽

Diels Alder Reaction ◽

Dimensional Cell

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ChemInform Abstract: Catalytic Asymmetric Inverse-Electron-Demand Oxa-Diels-Alder Reaction of in situ Generated ortho-Quinone Methides with 3-Methyl-2-vinylindoles.

ChemInform ◽

10.1002/chin.201536172 ◽

2015 ◽

Vol 46 (36) ◽

pp. no-no

Author(s):

Jia-Jia Zhao ◽

Si-Bing Sun ◽

Sai-Huan He ◽

Qiong Wu ◽

Feng Shi

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Quinone Methides ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Catalytic Asymmetric ◽

Electron Demand

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Accelerated Diels–Alder reaction of quinones generated in situ by a modified electrode in an aqueous sodium dodecyl sulfate micellar system

Chemical Communications ◽

10.1039/a703113k ◽

1997 ◽

pp. 1403-1404 ◽

Cited By ~ 23

Author(s):

Kazuhiro Chiba ◽

Madoka Jinno ◽

Ayako Nozaki ◽

Masahiro Tada

Keyword(s):

Sodium Dodecyl Sulfate ◽

Modified Electrode ◽

Sodium Dodecyl ◽

Alder Reaction ◽

Diels Alder ◽

Micellar System ◽

Aqueous Sodium ◽

Diels Alder Reaction ◽

Dodecyl Sulfate

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ChemInform Abstract: In situ Enamine Activation in Aqueous Salt Solutions. Highly Efficient Asymmetric Organocatalytic Diels-Alder Reaction of Cyclohexenones with Nitroolefins.

ChemInform ◽

10.1002/chin.200938063 ◽

2009 ◽

Vol 40 (38) ◽

Author(s):

Dan-Qian Xu ◽

Ai-Bao Xia ◽

Shu-Ping Luo ◽

Jie Tang ◽

Shuai Zhang ◽

...

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Salt Solutions ◽

Highly Efficient ◽

Diels Alder Reaction ◽

Aqueous Salt Solutions

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Mechanochemical milling promoted solvent-free imino Diels–Alder reaction catalyzed by FeCl3: diastereoselective synthesis of cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines

RSC Advances ◽

10.1039/c4ra05252h ◽

2014 ◽

Vol 4 (67) ◽

pp. 35635-35638 ◽

Cited By ~ 29

Author(s):

Ya-Jun Tan ◽

Ze Zhang ◽

Fang-Jian Wang ◽

Hao-Hao Wu ◽

Qing-Hai Li

Keyword(s):

Ball Milling ◽

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Diastereoselective Synthesis ◽

Diels Alder Reaction ◽

Mechanochemical Milling

Cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines were diastereoselectively synthesized by FeCl3-promoted solvent-free Diels–Alder reaction of in situ generated imine with styrene under ball milling.

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The Inverse Demand Oxa-Diels–Alder Reaction of Resorcinarenes: An Experimental and Theoretical Analysis of Regioselectivity and Diastereoselectivity

The Journal of Organic Chemistry ◽

10.1021/acs.joc.6b01099 ◽

2016 ◽

Vol 81 (14) ◽

pp. 6018-6025 ◽

Cited By ~ 8

Author(s):

Karolina Stefańska ◽

Hanna Jędrzejewska ◽

Michał Wierzbicki ◽

Agnieszka Szumna ◽

Waldemar Iwanek

Keyword(s):

Theoretical Analysis ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Inverse Demand

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