Biologically-modified Amino Acids
Biologically modified amino acids are derivatives arising from natural post-translational or metabolic modifications
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-0007651 -
In-stockPurity: ≥98%
Cat. No. : CS-0010219 -
In-stockPurity: 99.95%
Cat. No. : CS-0014213 -
In-stockPurity: 98.0%
Cat. No. : CS-0019764 -
In-stockPurity: ≥95%
Cat. No. : CS-0040590 -
In-stockPurity: ≥98%
Cat. No. : CS-0059319 -
In-stockPurity: ≥98%
Cat. No. : CS-0059346 -
In-stockPurity: ≥97%
Cat. No. : CS-0059358 -
In-stockPurity: ≥97%
Cat. No. : CS-0059465 -
In-stockPurity: ≥97%
Cat. No. : CS-0062451