95602-10-1

Upstream product

• 928-96-1 (Z)-3-Hexen-1-ol 
• 127-65-1 chloroamine-T 
• 95601-89-1 C₁₄H₁₉NO₄S 
• 4083-64-1 Tosyl isocyanate 
• 94953-06-7 (R)-4-((R)-1-Iodo-propyl)-3-(toluene-4-sulfonyl)-[1,3]oxazinan-2-one 

Relevant academic research and scientific papers

Scalable synthesis of N -acylaziridines from N -tosylaziridines

N-Acylaziridines are important starting materials for the synthesis of chiral amine derivatives. The traditional methods for producing these activated aziridines have significant drawbacks. The gram scale synthesis of N-acylaziridines by deprotection of N

CARBAMATE MEDIATED FUNCTIONALIZATION OF UNSATURATED ALCOHOLS II. REGIO- AND STEREO-SELECTIVE SYNTHESIS OF 1,3-SYN AND 1,2-ANTI AMINO ALCOHOL DERIVATIVES VIA IODOCARBAMATION

A regio- and stereo-selective introduction of nitrogen functions to double bonds of acyclic, allylic and homoallylic alcohols was achieved via iodocyclization of the corresponding N-sulfonylated O-carbamates.