© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimWe have developed a Hosomi-Sakurai type carbocyclization of homoallylic silyl ethers in reaction with silyl nucleophiles, catalyzed by Lewis acidic silylium salt. It offers cyclopropane and cyclobutane products with high efficiency and selectivity. A range of silyl nucleophiles could be engaged in this transformation to give small-sized carbocycles incorporating allyl, allenyl, carbonyl, indole or thioether groups. Diastereoselectivity in the cyclobutane formation was observed to be dependent on the steric bulkiness of incoming nucleophiles.11sciescopu
The versatility of intramolecular carbolithiation of simple unactivated alkenes to yield cyclopentyl...
Simple propargylic silyl ethers can be converted to complex cyclopropylboronic acid pinacol esters i...
The synthesis of siloles with substitution patterns that are continuative toward natural product syn...
The organoborane-catalyzed reductive carbocyclization of homoallylic alcohols has been developed by ...
Cyclopropanes and cyclobutanes, when activated with donor and acceptor groups, provide facile access...
The reaction of geraniol with different lithium carbenoids generated from n-BuLi and the correspondi...
A novel Lewis acid-catalyzed cycloisomerization of alkylidenecyclopropane acylsilanes is disclosed. ...
1,1-Bis(trimethylsilyloxy)ketene acetals represent useful synthetic building blocks which can be reg...
Based on our group’s previous study on chemoselective partial reduction of silyl-protected sugars an...
En este artículo de investigación se describe la síntesis de silil ciclopropanos a partir de eninona...
En este artículo de investigación se describe la síntesis de silil ciclopropanos a partir de eninona...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
Typescript (photocopy).An intermolecular-intramolecular Michael reaction sequence was developed for ...
Carbocycles are a key and widely present structural motif in organic compounds. The construction of ...
The three-component coupling of Mg acetylides, silyl glyoxylates, and nitroalkenes results in a high...
The versatility of intramolecular carbolithiation of simple unactivated alkenes to yield cyclopentyl...
Simple propargylic silyl ethers can be converted to complex cyclopropylboronic acid pinacol esters i...
The synthesis of siloles with substitution patterns that are continuative toward natural product syn...
The organoborane-catalyzed reductive carbocyclization of homoallylic alcohols has been developed by ...
Cyclopropanes and cyclobutanes, when activated with donor and acceptor groups, provide facile access...
The reaction of geraniol with different lithium carbenoids generated from n-BuLi and the correspondi...
A novel Lewis acid-catalyzed cycloisomerization of alkylidenecyclopropane acylsilanes is disclosed. ...
1,1-Bis(trimethylsilyloxy)ketene acetals represent useful synthetic building blocks which can be reg...
Based on our group’s previous study on chemoselective partial reduction of silyl-protected sugars an...
En este artículo de investigación se describe la síntesis de silil ciclopropanos a partir de eninona...
En este artículo de investigación se describe la síntesis de silil ciclopropanos a partir de eninona...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
Typescript (photocopy).An intermolecular-intramolecular Michael reaction sequence was developed for ...
Carbocycles are a key and widely present structural motif in organic compounds. The construction of ...
The three-component coupling of Mg acetylides, silyl glyoxylates, and nitroalkenes results in a high...
The versatility of intramolecular carbolithiation of simple unactivated alkenes to yield cyclopentyl...
Simple propargylic silyl ethers can be converted to complex cyclopropylboronic acid pinacol esters i...
The synthesis of siloles with substitution patterns that are continuative toward natural product syn...