Synthesis of polynorbornene with pendant moiety bearing azide and terminal alkyne groups was written by Zhang, Ze;Peng, Zhi Wei;Fan, Kun Zeng. And the article was included in Chinese Chemical Letters in 2011.Recommanded Product: 368435-46-5 The following contents are mentioned in the article:
A powerful approach to the synthesis of an unprecedented polynorbornene with pendant moiety bearing azide and terminal alkyne groups is developed. Two key intermediates, namely, 3-azido-5-(2-(trimethylsilyl)ethynyl) benzyl alc. and 4-(4-aza-tricyclo [5.2.1.02.6]dec-8-en-4-yl) benzoic acid, were optimally synthesized for convergent synthesis of the corresponding monomer. This study involved multiple reactions and reactants, such as (3-Amino-5-iodophenyl)methanol (cas: 368435-46-5Recommanded Product: 368435-46-5).
(3-Amino-5-iodophenyl)methanol (cas: 368435-46-5) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Recommanded Product: 368435-46-5
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com