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DI-TERT-BUTYL AZODICARBOXYLATE, 98%
Кат. №: 135992-25G
Производитель: Sigma-Aldrich
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DI-TERT-BUTYL AZODICARBOXYLATE, 98%
Main image
Кат. №: 135992-25G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
DI-TERT-BUTYL AZODICARBOXYLATE, 98%
Кат. №: 135992-25G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Description General description We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Application Co-oxidant in copper-catalyzed greener oxidation of alcohols under aerobic conditions. Modified Markó’s aerobic oxidation of alcohols under atmospheric pressure with air or molecular oxygen at room temperature Reactant for: • Preparation of hexapeptide key fragments via stereoselective selenocyclization/oxidative deselenylation or hydrazination/cyclization reactions • Asymmetric Michael addition reactions • Preparation of dipeptidyl peptidase IV dependent water-soluble prodrugs via Mitsunobu reaction • Synthesis of pyrroloisoquinoline template via stereoselective N-acyliminium-mediated cyclization and enolate amination for synthesis of peptidomimetic compounds • Barbier-type propargylation reactions • Synthesis of bacterial peptide deformylase (PDF) inhibitor fumimycin • Asymmetric amination of glycine Schiff bases Packaging 5, 25 g in glass bottle
Related Categories
12 Principles Aligned Products, C-X Bond Formation (Non-Halogen), Chemical Synthesis, Greener Alternative Products, Greener Synthetic Reagents, Mitsunobu, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description General description We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Application Co-oxidant in copper-catalyzed greener oxidation of alcohols under aerobic conditions. Modified Markó’s aerobic oxidation of alcohols under atmospheric pressure with air or molecular oxygen at room temperature Reactant for: • Preparation of hexapeptide key fragments via stereoselective selenocyclization/oxidative deselenylation or hydrazination/cyclization reactions • Asymmetric Michael addition reactions • Preparation of dipeptidyl peptidase IV dependent water-soluble prodrugs via Mitsunobu reaction • Synthesis of pyrroloisoquinoline template via stereoselective N-acyliminium-mediated cyclization and enolate amination for synthesis of peptidomimetic compounds • Barbier-type propargylation reactions • Synthesis of bacterial peptide deformylase (PDF) inhibitor fumimycin • Asymmetric amination of glycine Schiff bases Packaging 5, 25 g in glass bottle
Related Categories
12 Principles Aligned Products, C-X Bond Formation (Non-Halogen), Chemical Synthesis, Greener Alternative Products, Greener Synthetic Reagents, Mitsunobu, Synthetic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.