Automated Synthesis of a Library of Triazolated 1,2,5-Thiadiazepane 1,1-Dioxides via a Double Aza-Michael Strategy
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文摘
The construction of a 96-member library of triazolated 1,2,5-thiadiazepane 1,1-dioxides was performed on a Chemspeed Accelerator (SLT-100) automated parallel synthesis platform, culminating in the successful preparation of 94 out of 96 possible products. The key step, a one-pot, sequential elimination, double-aza-Michael reaction, and [3 + 2] Huisgen cycloaddition pathway has been automated and utilized in the production of two sets of triazolated sultam products.

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org/action/doSearch?action=search&searchText=aza%5C-Michael&qsSearchArea=searchText">aza-Michael; org/action/doSearch?action=search&searchText=triazolated+1%2C2%2C5%5C-thiadiazepane+1%2C1%5C-dioxides&qsSearchArea=searchText">triazolated 1,2,5-thiadiazepane 1,1-dioxides; org/action/doSearch?action=search&searchText=parallel+synthesis&qsSearchArea=searchText">parallel synthesis

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