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DICHLOROPHENYLBORANE, 97%
Кат. №: 101346-1G
Производитель: Sigma-Aldrich
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DICHLOROPHENYLBORANE, 97%
Main image
Кат. №: 101346-1G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
DICHLOROPHENYLBORANE, 97%
Кат. №: 101346-1G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Application Catalyst for: • Antiproliferative macrolide and cell migration inhibitor lactimidomycin • Enantioselective synthesis of polyketide segments using vinylogous Mukaiyama aldol reactions • Enantioselective Diels-Alder cycloadditions after its reaction with allo-threonine derivatives • Stereoselective alkylative ring opening of cyclic anhydrides • Cross-metathesis reaction of amino derivatives with olefins • Asymmetric acetate aldol reactions • The reaction of aryl aldehydes with styrene and (E)-β-methylstyrene Dichlorophenylborane can be used as a catalyst for: • The synthesis of an antiproliferative macrolide and cell migration inhibitor lactimidomycin. • Enantioselective synthesis of polyketide segments using vinylogous Mukaiyama aldol reactions. • Enantioselective Diels-Alder cycloadditions after its reaction with allo-threonine derivatives. • Stereoselective alkylative ring opening of cyclic anhydrides. • Cross-metathesis reaction of amino derivatives with olefins. • Asymmetric acetate aldol reactions. Packaging 1, 5, 25 g in glass bottle
Related Categories
Boranes, Chemical Synthesis, Reduction, Synthetic Reagents Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Application Catalyst for: • Antiproliferative macrolide and cell migration inhibitor lactimidomycin • Enantioselective synthesis of polyketide segments using vinylogous Mukaiyama aldol reactions • Enantioselective Diels-Alder cycloadditions after its reaction with allo-threonine derivatives • Stereoselective alkylative ring opening of cyclic anhydrides • Cross-metathesis reaction of amino derivatives with olefins • Asymmetric acetate aldol reactions • The reaction of aryl aldehydes with styrene and (E)-β-methylstyrene Dichlorophenylborane can be used as a catalyst for: • The synthesis of an antiproliferative macrolide and cell migration inhibitor lactimidomycin. • Enantioselective synthesis of polyketide segments using vinylogous Mukaiyama aldol reactions. • Enantioselective Diels-Alder cycloadditions after its reaction with allo-threonine derivatives. • Stereoselective alkylative ring opening of cyclic anhydrides. • Cross-metathesis reaction of amino derivatives with olefins. • Asymmetric acetate aldol reactions. Packaging 1, 5, 25 g in glass bottle
Related Categories
Boranes, Chemical Synthesis, Reduction, Synthetic Reagents Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.