Intermolecular enol ether-alkyne metathesis

Organic Letters

Volumn 5, Issue 10, 2003, Pages 1793-1796

  Giessert, Anthony J ^a   Snyder, Lee ^a   Markham, Jordan ^a   Diver, Steven T ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL ETHER; ALKYNE DERIVATIVE; ETHER DERIVATIVE; ALKYNE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; RUTHENIUM DERIVATIVE;

ADDITION REACTION; ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CYCLOADDITION; ELECTRON; REACTION ANALYSIS; RING CLOSING METATHESIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; CHEMISTRY; CYCLIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

ALKYNES; CYCLIZATION; ELECTRONS; ETHERS; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; RUTHENIUM COMPOUNDS; STEREOISOMERISM;

EID: 0042229213     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034459k     Document Type: Article

References (21)

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19. Literature yields for cycloadditions with dienol ethers use excess dienol ether and base yields on the reactive (E)-isomer. (a) Mandai, T.; Osaka, K.; Kawagishi, M.; Kawada, M.; Otera, J. J. Org. Chem. 1984, 49, 3595-3600. (b) Shibata, J.; Shiina, I.; Mukaiyama, T. Chem. Lett. 1999, 313-314. (c) Mikami, K.; Motoyama, Y.; Terada, M. J. Am. Chem. Soc. 1994, 116, 2812-2820.
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21. Literature yields for cycloadditions with dienol ethers use excess dienol ether and base yields on the reactive (E)-isomer. (a) Mandai, T.; Osaka, K.; Kawagishi, M.; Kawada, M.; Otera, J. J. Org. Chem. 1984, 49, 3595-3600. (b) Shibata, J.; Shiina, I.; Mukaiyama, T. Chem. Lett. 1999, 313-314. (c) Mikami, K.; Motoyama, Y.; Terada, M. J. Am. Chem. Soc. 1994, 116, 2812-2820.