Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings

10.1039/c5sc01614b

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Main Authors: Wang, T, Yu, Z, Hoon, D.L, Huang, K.-W, Lan, Y, Lu, Y
Other Authors: CHEMISTRY
Format: Article
Published: Royal Society of Chemistry 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/175496
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spelling sg-nus-scholar.10635-1754962024-04-24T09:57:28Z Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings Wang, T Yu, Z Hoon, D.L Huang, K.-W Lan, Y Lu, Y CHEMISTRY Addition reactions Catalysis Enantioselectivity Hydrogen bonds Stereochemistry Asymmetric induction Bi-functional Chiral centers DFT calculation Donor molecules Enantioselective Enantioselective construction Hydrogen bonding interactions Phosphorus compounds 10.1039/c5sc01614b Chemical Science 6 8 4912-4922 2020-09-10T01:53:37Z 2020-09-10T01:53:37Z 2015 Article Wang, T, Yu, Z, Hoon, D.L, Huang, K.-W, Lan, Y, Lu, Y (2015). Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings. Chemical Science 6 (8) : 4912-4922. ScholarBank@NUS Repository. https://doi.org/10.1039/c5sc01614b 20416520 https://scholarbank.nus.edu.sg/handle/10635/175496 Royal Society of Chemistry Unpaywall 20200831
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic Addition reactions
Catalysis
Enantioselectivity
Hydrogen bonds
Stereochemistry
Asymmetric induction
Bi-functional
Chiral centers
DFT calculation
Donor molecules
Enantioselective
Enantioselective construction
Hydrogen bonding interactions
Phosphorus compounds
spellingShingle Addition reactions
Catalysis
Enantioselectivity
Hydrogen bonds
Stereochemistry
Asymmetric induction
Bi-functional
Chiral centers
DFT calculation
Donor molecules
Enantioselective
Enantioselective construction
Hydrogen bonding interactions
Phosphorus compounds
Wang, T
Yu, Z
Hoon, D.L
Huang, K.-W
Lan, Y
Lu, Y
Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
description 10.1039/c5sc01614b
author2 CHEMISTRY
author_facet CHEMISTRY
Wang, T
Yu, Z
Hoon, D.L
Huang, K.-W
Lan, Y
Lu, Y
format Article
author Wang, T
Yu, Z
Hoon, D.L
Huang, K.-W
Lan, Y
Lu, Y
author_sort Wang, T
title Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
title_short Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
title_full Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
title_fullStr Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
title_full_unstemmed Highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5H-thiazol-4-ones and 5H-oxazol-4-ones: scope and mechanistic understandings
title_sort highly enantioselective construction of tertiary thioethers and alcohols via phosphine-catalyzed asymmetric ?-addition reactions of 5h-thiazol-4-ones and 5h-oxazol-4-ones: scope and mechanistic understandings
publisher Royal Society of Chemistry
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/175496
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