1333239-52-3

Upstream product

• 4117-10-6 6-hepten-1-ol 
• 1333331-55-7 C₃₅H₅₄FN₃O₈Si 
• 1333239-46-5 C₄₂H₆₇N₃O₉Si 

Downstream Products

• 1333239-66-9 C₃₇H₅₃N₃O₉ 
• 1333239-79-4 tert-butyl (((11S,12R)-17-amino-14-((S)-1-((4-methoxybenzyl)-oxy)prop-2-yl)-12-methyl-15-oxo-3,4,5,6,7,8,9,11,12,13,14,15-dodecahydro-2H-benzo[b][1,9,5]dioxaazacycloheptadec-11-yl)methyl)(methyl)carbamate 
• 1333239-58-9 tert-butyl ((2R,3R)-2-(allyloxy)-4-(2-(hept-6-en-1-yloxy)-N-((S)-1-((4-methoxybenzyl)-oxy)prop-2-yl)-5-nitrobenzamido)-3-methylbutyl)(methyl)carbamate 

Relevant academic research and scientific papers

Diversity-oriented synthesis of 13- to 18-membered macrolactams via ring-closing metathesis

An efficient build/couple/pair approach to diversity-oriented synthesis was employed to access several structurally complex macrolactams. In this paper, we describe the successful evaluation of ring-closing metathesis toward the systematic generation of skeletal diversity. By appropriately varying the nature and chain length of the alkenol fragment, a diverse collection of 13- to 18-membered macro-lactams were obtained.