Triflate Formation
Triflate Formation usually involves the reaction of alcohols with trifluoromethanesulfonic acid or trifluoromethanesulfonic acid esterification reagents, and the resulting triflesulfonic acid ester is widely used in organic synthesis as an excellent leaving group or intermediate.
Technical Resources
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Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiralChiral chloro-indeno pybox has served as a new ligand for the Yb(OTf)3-catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with nitroalkenes. The tunable nature of pybox ligands
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2Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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3Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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4Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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5Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
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In-stockPurity: ≥98%
Cat. No. : CS-0129461CAS No. : 29540-81-6* This product is not sold in the region.
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In-stockPurity: ≥98%
Cat. No. : CS-0156098CAS No. : 456-64-4* This product is not sold in the region.
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In-stockPurity: ≥96%
Cat. No. : CS-B0879CAS No. : 37595-74-7* This product is not sold in the region.
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In-stockPurity: ≥98%
Cat. No. : CS-M2922CAS No. : 17763-80-3* This product is not sold in the region.
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In-stockPurity: ≥95%
![2-[N,N-Bis(trifluoromethylsulfonyl)amino]-5-chloropyridine|CS-W009001](https://file.chemscene.com/productPIC/CS-W009001.gif)
Cat. No. : CS-W009001CAS No. : 145100-51-2* This product is not sold in the region.
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In-stockPurity: ≥95%
Cat. No. : CS-W021265CAS No. : 145100-50-1* This product is not sold in the region.