A frontier molecular orbital treatment of fulvene cycloadditions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference57 articles.
1. Novel double [6 + 4] cycloaddition of tropone to dimethylfulvene
2. Elucidation of the structure of the double [6 + 4]adduct of tropone and dimethylfulvene by nuclear magnetic resonance and the nuclear overhauser effect
3. Stereoselective [6 + 4] cycloadditions of methylfulvene and phenylfulvene to tropone
4. Cycloadditions of tropone and diphenylnitrileimine: A [6+4] 1,3-dipolar cycloaddition
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1. Rearrangement of a carboxy-substituted spiro[4.4]nonatriene to annulated fulvenes through a Pd(ii)-mediated 1,5-vinyl shift;Chemical Science;2023
2. An overview of the cycloaddition chemistry of fulvenes and emerging applications;Beilstein Journal of Organic Chemistry;2019-09-06
3. Tuning of the Electro-Optical Properties of Tetraphenylcyclopentadienone via Substitution of Oxygen with Sterically-Hindered Electron Withdrawing Groups;Scientific Reports;2019-09-04
4. Catalytic Enantioselective [10+4] Cycloadditions;Angewandte Chemie International Edition;2018-10
5. Catalytic Enantioselective [10+4] Cycloadditions;Angewandte Chemie;2018-09-07
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