Synthesis of Chiral 3′-Hydroxy-γ-ionylideneacetic Acids
نویسندگان
چکیده
منابع مشابه
Enzymatic synthesis of chiral γ-amino acids using ω-transaminase.
In this study, we successfully synthesized enantiomerically pure (R)- and (S)-γ-amino acids (>99% ee) using ω-transaminase (ω-TA) through kinetic resolution and asymmetric synthesis respectively. The present study demonstrates the high potentiality of ω-TA reaction for the production of chiral γ-amino acids.
متن کاملSynthesis of chiral α-hydroxy acids via palladium-catalyzed C(sp(3))-H alkylation of lactic acid.
Herein we report a Pd-catalyzed alkylation of lactic acid with the assistance of 8-aminoquinoline auxiliary. A wide range of alkyl iodides bearing β-hydrogen atoms are compatible with the reaction conditions, providing a practical and straightforward alternative to access chiral α-hydroxy acids (AHAs). The new reactions have been applied for the synthesis of isotope-labeled AHAs and a sugar-con...
متن کاملSynthesis of chiral a-hydroxy acids via palladium- catalyzed C(sp)–H alkylation of lactic acid†
Herein we report a Pd-catalyzed alkylation of lactic acid with the assistance of 8-aminoquinoline auxiliary. A wide range of alkyl iodides bearing b-hydrogen atoms are compatible with the reaction conditions, providing a practical and straightforward alternative to access chiral a-hydroxy acids (AHAs). The new reactions have been applied for the synthesis of isotope-labeled AHAs and a sugarcont...
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The conformation of hydroxy-γ-ionylideneacetic acids produced by Cercospora cruenta was examined by 'H-NMR analysis. (1)H-(1)H COSY and NOE data indicated that (2Z,4E,1'R,4'#)-4'-hydroxy-(γ)- ionylideneacetic acid has a cyclohexane ring of chair form furnishing a hydroxyl group and a 2,4-pentadienoic acid moiety, each with equatorial orientation, while (2Z,4E,1'S,3'S)-3'-hydroxy-γ-ionylideneace...
متن کاملThe asymmetric synthesis of chiral cyclic α-hydroxy phosphonates and quaternary cyclic α-hydroxy phosphonates.
A highly practical, catalytic enantioselective cyclic phosphite addition to aldehydes and ketones was developed. The reaction rate of the asymmetric hydrophosphonylation was significantly enhanced by the addition of silver carbonate. Particularly, significant improvement has been achieved on the asymmetric hydrophosphonylation of unactivated ketones, giving quaternary α-hydroxy phosphonates wit...
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ژورنال
عنوان ژورنال: Agricultural and Biological Chemistry
سال: 1988
ISSN: 0002-1369
DOI: 10.1080/00021369.1988.10869011