Mitsunobu Reaction
Mitsunobu reactions can convert alcohols into various other functional groups, such as esters, ethers, and azides, often with high stereoselectivity. It is often used in the synthesis of drugs and natural products.
Technical Resources
-
1
1
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
-
2Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
-
3Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
-
4Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
-
5Catalytic asymmetric Friedel–Crafts alkylation of unprotected indoles with nitroalkenes using a novel chiral
-
In-stockPurity: ≥98%
Cat. No. : CS-0020124 -
In-stockPurity: ≥98%
Cat. No. : CS-0035166 -
In-stockPurity: ≥98%
Cat. No. : CS-0035238CAS No. : 739-58-2* This product is not sold in the region.
-
In-stockPurity: ≥95%
Cat. No. : CS-0046100CAS No. : 157141-27-0* This product is not sold in the region.
-
In-stockPurity: ≥97%
Cat. No. : CS-0085776 -
In-stockPurity: ≥97%
Cat. No. : CS-0132125 -
In-stockPurity: ≥95%
Cat. No. : CS-0156067 -
In-stockPurity: ≥97%
Cat. No. : CS-D1520 -
In-stockPurity: ≥98%
Cat. No. : CS-W001467CAS No. : 16466-61-8* This product is not sold in the region.
-
In-stockPurity: ≥95%
Cat. No. : CS-W014059