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pro vyhledávání: '"Marcus Wen Yao Lee"'
Publikováno v:
Organic Letters. 21:5990-5994
A nickel-catalyzed reductive cyclization of enones affords a wide array of indanones in high enantiomeric induction. The reaction is featured with an unprecedented broad scope of substrates. The versatility of the new method is demonstrated in severa
Publikováno v:
Angewandte Chemie International Edition. 56:12723-12726
A nickel‐catalyzed asymmetric reductive Heck reaction of aryl chlorides has been developed that affords substituted indolines with high enantioselectivity. Manganese powder is used as the terminal reductant with water as a proton source. Mechanisti
Publikováno v:
Organic letters. 21(15)
A nickel-catalyzed reductive cyclization of enones affords a wide array of indanones in high enantiomeric induction. The reaction is featured with an unprecedented broad scope of substrates. The versatility of the new method is demonstrated in severa