Enantioselective synthesis of flavan-3-ols using a mitsunobu cyclization

Synthesis

Volumn , Issue 5, 2009, Pages 779-786

  Krohn, Karsten ^a   Ahmed, Ishtiaq ^a   John, Markus ^b  

^a UNIVERSITY OF PADERBORN   (Germany)

^b Macherey Nagel GmbH and Co KG   (Germany)

Author keywords

Flavanol synthesis; Mitsunobu reaction; Myristinin a; Sharpless dihydroxylation

Indexed keywords

CHIRAL HPLC; COUPLING PRODUCTS; CYCLIZATION PRODUCTS; DNA POLYMERASE; ELECTRON DENSITIES; ENANTIO-SELECTIVE SYNTHESIS; ENANTIOSELECTIVE; FIVE-MEMBERED RINGS; FLAVAN-3-OLS; FLAVANOL SYNTHESIS; MITSUNOBU CYCLIZATION; MITSUNOBU REACTION; MYRISTININ A; PROCYANIDINS; SHARPLESS DIHYDROXYLATION; STARTING MATERIALS; SUBSTITUTION PATTERNS;

CYCLIZATION; ENANTIOSELECTIVITY; NUCLEIC ACIDS; OLEFINS; OLIGOMERS;

SYNTHESIS (CHEMICAL);

ALKENE DERIVATIVE; DNA DIRECTED DNA POLYMERASE BETA; FLAVANOL DERIVATIVE; MYRISTININ A; PROCYANIDIN DERIVATIVE; TRANSFERASE INHIBITOR; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DIHYDROXYLATION; ELECTRON; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MITSUNOBU REACTION; STEREOCHEMISTRY;

EID: 63449112305     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1083361     Document Type: Article

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