Enantiopure, C3-symmetric trialkanolamines can be efficiently and rapidly obtained on a gram scale via one pot or step-wise microwave-assisted epoxide ring opening with ammonia in high yields (up to 89%) and regioselectivity up to 100%.
Highly Regioselective Microwave-Assisted Synthesis of Enantiopure C3-Symmetric Trialkanolamines
LICINI, GIULIA MARINA
2002
Abstract
Enantiopure, C3-symmetric trialkanolamines can be efficiently and rapidly obtained on a gram scale via one pot or step-wise microwave-assisted epoxide ring opening with ammonia in high yields (up to 89%) and regioselectivity up to 100%.File in questo prodotto:
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