Total synthesis of (+)-lactiflorin by an intramolecular [2+2] photocycloaddition

Angewandte Chemie - International Edition

Volumn 51, Issue 5, 2012, Pages 1261-1264

  Lu, Ping ^a   Bach, Thorsten ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

cycloaddition; glycosylation; photochemistry; structure elucidation; total synthesis

Indexed keywords

ANALYTICAL DATA; DIFFERENT STRUCTURE; NATURAL PRODUCTS; PHOTOCYCLOADDITION; PHOTOCYCLOADDITION REACTION; STEREOSELECTIVE SYNTHESIS; STRUCTURE ELUCIDATION; TOTAL SYNTHESIS;

CYCLOADDITION; GLYCOSYLATION; PHOTOCHEMICAL REACTIONS; STEREOCHEMISTRY; STEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

GLYCOSIDE; LACTIFLORIN; TERPENE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; METABOLISM; NUCLEAR MAGNETIC RESONANCE; PHOTOCHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CYCLIZATION; GLYCOSIDES; MOLECULAR STRUCTURE; MONOTERPENES; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHOTOCHEMICAL PROCESSES; STEREOISOMERISM;

EID: 84856195864     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106889     Document Type: Article

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