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Methodologies in Asymmetric Catalysis
Author(s) -
Sanjay V. Malhotra
Publication year - 2004
Publication title -
acs symposium series
Language(s) - English
Resource type - Book series
SCImago Journal Rank - 0.169
H-Index - 64
eISSN - 1947-5918
pISSN - 0097-6156
DOI - 10.1021/bk-2004-0880
Subject(s) - catalysis , cyclopropanation , intramolecular force , ylide , lewis acids and bases , chemistry , reuse , carbon fibers , combinatorial chemistry , organic chemistry , materials science , waste management , composite material , composite number , engineering
Asymmetric hydrogenation has been demonstrated to be a useful synthetic approach to amino acids and derivatives. The asymmetric reduction step itself is usually straightforward, but the synthesis of the ligand that invokes the asymmetric induction can be difficult. Use of MonoPhos™, a phosphoramidite, allows for a low cost solution as it is derived in a single step from BINOL, an item of commerce available as either antipode. Rhodium catalyzed asymmetric hydrogenations proceed with high enantioselectivities, especially to substituted phenylalanine derivatives. A large solvent effect is observed

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