Quinolyne Precursors
Quinoline precursors typically involve compounds with aromatic rings and nitrogen atoms.
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: ≥97%
Cat. No. : CS-0041399 -
In-stockPurity: ≥96%
Cat. No. : CS-W002501 -
In-stockPurity: ≥97%
Cat. No. : CS-W002559 -
In-stockPurity: ≥96%
Cat. No. : CS-W004432 -
In-stockPurity: ≥97%
Cat. No. : CS-W007403 -
In-stockPurity: ≥98%
Cat. No. : CS-W007925 -
In-stockPurity: ≥97%
Cat. No. : CS-W019978