Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction

Ryan Kenny, Peter Karuso, Hans Senn, Fei Liu

Research output: Chapter in Book/Report/Conference proceedingOther chapter contributionResearch

LanguageEnglish
Title of host publicationRACI NSW Organic Chemistry Group 36th annual one-day symposium
Subtitle of host publicationprogramme
Place of PublicationMelbourne
PublisherRoyal Australian Chemical Institute
Pages43
Number of pages1
ISBN (Print)9781741384369
Publication statusPublished - 2015
EventRACI NSW Organic Chemistry Group annual one-day symposium (36th : 2015) - Macquarie University, New South Wales
Duration: 2 Dec 20152 Dec 2015

Conference

ConferenceRACI NSW Organic Chemistry Group annual one-day symposium (36th : 2015)
CityMacquarie University, New South Wales
Period2/12/152/12/15

Cite this

Kenny, R., Karuso, P., Senn, H., & Liu, F. (2015). Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction. In RACI NSW Organic Chemistry Group 36th annual one-day symposium: programme (pp. 43). Melbourne: Royal Australian Chemical Institute.
Kenny, Ryan ; Karuso, Peter ; Senn, Hans ; Liu, Fei. / Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction. RACI NSW Organic Chemistry Group 36th annual one-day symposium: programme. Melbourne : Royal Australian Chemical Institute, 2015. pp. 43
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Kenny, R, Karuso, P, Senn, H & Liu, F 2015, Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction. in RACI NSW Organic Chemistry Group 36th annual one-day symposium: programme. Royal Australian Chemical Institute, Melbourne, pp. 43, RACI NSW Organic Chemistry Group annual one-day symposium (36th : 2015), Macquarie University, New South Wales, 2/12/15.

Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction. / Kenny, Ryan; Karuso, Peter; Senn, Hans; Liu, Fei.

RACI NSW Organic Chemistry Group 36th annual one-day symposium: programme. Melbourne : Royal Australian Chemical Institute, 2015. p. 43.

Research output: Chapter in Book/Report/Conference proceedingOther chapter contributionResearch

TY - CHAP

T1 - Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction

AU - Kenny, Ryan

AU - Karuso, Peter

AU - Senn, Hans

AU - Liu, Fei

PY - 2015

Y1 - 2015

M3 - Other chapter contribution

SN - 9781741384369

SP - 43

BT - RACI NSW Organic Chemistry Group 36th annual one-day symposium

PB - Royal Australian Chemical Institute

CY - Melbourne

ER -

Kenny R, Karuso P, Senn H, Liu F. Structural basis to enantioselective proton transfer by acid-activated trifunctional organocatalysts in the aza-Morita-Baylis-Hillman reaction. In RACI NSW Organic Chemistry Group 36th annual one-day symposium: programme. Melbourne: Royal Australian Chemical Institute. 2015. p. 43