1033811-99-2Relevant academic research and scientific papers
Efficient synthesis of the indoloazocine framework via intramolecular alkyne carbocyclization
Donets, Pavel A.,Hecke, Kristof Van,Meervelt, Luc Van,Van Der Eycken, Erik V.
supporting information; experimental part, p. 3618 - 3621 (2011/02/23)
Image Presented A microwave-assisted protocol based on an Hg(OTf) 2 catalyzed intramolecular alkyne carbocyclization reaction was developed for selective construction of the indoloazocine core.
Ranging correlated motion (1.5 nm) of two coaxially arranged rotors mediated by helix inversion of a supramolecular transmitter
Hiraoka, Shuichi,Okuno, Erika,Tanaka, Takaaki,Shiro, Motoo,Shionoya, Mitsuhiko
supporting information; experimental part, p. 9089 - 9098 (2009/02/03)
For a long-range transmission of motion between two movable parts apart from each other, transmitters that can precisely correlate these two motions should be properly incorporated into the system. However, such a motional relay is yet to be realized in a
Efficient synthesis of the 3-benzazepine framework via intramolecular heck reductive cyclization
Donets, Pavel A.,Van Der Eycken, Erik V.
, p. 3017 - 3020 (2008/02/09)
A microwave-assisted protocol based on reductive Heck reaction was developed for regio- and stereoselective construction of the 3-benzazepine core.
A convenient synthesis of chiral 2-alkynyl-1,3-oxazolines
Cevallos, Alexandre,Rios, Ramon,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni
, p. 4407 - 4416 (2007/10/03)
A general, high-yielding, two-step synthesis of chiral 2-alkynyl-1,3-oxazolines starting from 2-alkynoic acids and 2-aminoalcohols is disclosed. (C) 2000 Published by Elsevier Science Ltd.
