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Angewandte Chemie - International Edition

Volumn 53, Issue 44, 2014, Pages 11931-11934

Synthesis of bis(indole) alkaloids from Arundo donax: The ynindole diels-alder reaction, conformational chirality, and absolute stereochemistry

(3) Chen, Jingjin a Ferreira, Andrew J a Beaudry, Christopher M a

a OREGON STATE UNIVERSITY (United States)

Author keywords

Alkynes; Chirality; Cycloaddition; Natural products; Total synthesis

Indexed keywords

ALKALOIDS; CHIRALITY; CYCLOADDITION; METABOLITES; NITROGEN COMPOUNDS; POLYCYCLIC AROMATIC HYDROCARBONS; STEREOCHEMISTRY; STEREOSELECTIVITY;

ABSOLUTE STEREOCHEMISTRY; ALKYNES; DIELS-ALDER REACTION; HALF LIVES; NATURAL PRODUCTS; ROOM TEMPERATURE; TOTAL SYNTHESIS;

SYNTHESIS (CHEMICAL);

ALKALOID; ALKYNE; BIOLOGICAL PRODUCT; INDOLE DERIVATIVE;

CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; CYCLOADDITION; STEREOISOMERISM; SYNTHESIS;

ALKALOIDS; ALKYNES; BIOLOGICAL PRODUCTS; CYCLOADDITION REACTION; INDOLES; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84915749701 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201407336 Document Type: Article

Times cited : (23)

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