SCOPUS 정보 검색 플랫폼

Volumn 8, Issue 15, 2010, Pages 3509-3517

A convergent approach to (R)-Tiagabine by a regio- and stereocontrolled hydroiodination of alkynes

(7) Bartoli, Giuseppe a Cipolletti, Roberto b Di Antonio, Giustino b,c Giovannini, Riccardo c Lanari, Silvia b Marcolini, Mauro b Marcantoni, Enrico b

a UNIVERSITY OF BOLOGNA (Italy)

b UNIVERSITY OF CAMERINO (Italy)

c Boehringer Ingelheim Italia SpA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOBUTYRIC ACIDS; BIOLOGICALLY ACTIVE MOLECULES; CARBON-CARBON TRIPLE BONDS; CONVERGENT APPROACH; NATURAL PRODUCTS; STEREOSELECTIVE FORMATION; SYNTHETIC APPLICATION; THIENYL; TOTAL SYNTHESIS;

ACETYLENE; AMINO ACIDS;

ACIDS;

ALKENE; ALKYNE; CERIUM; CERIUM CHLORIDE; NIPECOTIC ACID DERIVATIVE; TIAGABINE; CEROUS CHLORIDE;

ARTICLE; CHEMISTRY; ELECTRON; ENZYME SPECIFICITY; HALOGENATION; STEREOISOMERISM;

ALKENES; ALKYNES; CERIUM; ELECTRONS; HALOGENATION; NIPECOTIC ACIDS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 77954641808 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c005042c Document Type: Article

Times cited : (28)

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