Asymmetric induction in the [2+2] cycloaddition of a keteniminium salt: an approach to chiral 13-oxa prostanoids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Type II intramolecular [2 + 2]-cycloaddition of alkenes with vinylketenes prepared by the regiospecific deprotonation of .beta.,.beta.-disubstituted .alpha.,.beta.-unsaturated acid chlorides
2. Preparation of unsaturated .alpha.-chloro acids and intramolecular [2 + 2] cycloadditions of the chloroketenes derived from them
3. Synthesis of terpenes containing the bicyclo[3.1.1]heptane ring system by the intramolecular [2 + 2] cycloaddition reaction of vinylketenes with alkenes. Preparation of chrysanthenone, .beta.-pinene, .beta.-cis-bergamotene, .beta.-trans-bergamotene, .beta.-copaene, and .beta.-ylangene and lemnalol
4. Intramolecular [2 + 2] cycloadditions of ketenes
5. Intramolecular [2 + 2] cycloadditions of alkoxyketenes and alkoxyketeniminium salts
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3. Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis;Synthesis;2017-07-17
4. Diastereoselective Intramolecular Carbamoylketene/Alkene [2 + 2] Cycloaddition: Enantioselective Access to Pyrrolidinoindoline Alkaloids;Organic Letters;2012-12-19
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