Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans

10.1021/acs.orglett.8b02519

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Main Authors: Jin, Zhichao, Ni, Huanzhen, Zhou, Bo, Zheng, Wenrui, Yixin, Lu
Other Authors: DEPT OF CHEMISTRY
Format: Article
Language:English
Published: AMER CHEMICAL SOC 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/170220
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Institution: National University of Singapore
Language: English
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spelling sg-nus-scholar.10635-1702202023-11-01T07:40:16Z Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans Jin, Zhichao Ni, Huanzhen Zhou, Bo Zheng, Wenrui Yixin, Lu DEPT OF CHEMISTRY Science & Technology Physical Sciences Chemistry, Organic Chemistry ELECTRON-DEFICIENT OLEFINS ALPHA-AMINO-ACID NATURAL-PRODUCTS ALPHA,BETA-UNSATURATED IMINES FUNCTIONALIZED CYCLOPENTENES ASYMMETRIC-SYNTHESIS POLYKETIDE SYNTHASE 3+2 CYCLOADDITIONS POLYCYCLIC ETHERS GAMMA-ADDITIONS 10.1021/acs.orglett.8b02519 ORGANIC LETTERS 20 17 5515-5518 2020-06-18T01:27:01Z 2020-06-18T01:27:01Z 2018-09-07 2020-06-17T04:11:21Z Article Jin, Zhichao, Ni, Huanzhen, Zhou, Bo, Zheng, Wenrui, Yixin, Lu (2018-09-07). Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans. ORGANIC LETTERS 20 (17) : 5515-5518. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.orglett.8b02519 1523-7060,1523-7052 https://scholarbank.nus.edu.sg/handle/10635/170220 en AMER CHEMICAL SOC Elements
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
language English
topic Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
ELECTRON-DEFICIENT OLEFINS
ALPHA-AMINO-ACID
NATURAL-PRODUCTS
ALPHA,BETA-UNSATURATED IMINES
FUNCTIONALIZED CYCLOPENTENES
ASYMMETRIC-SYNTHESIS
POLYKETIDE SYNTHASE
3+2 CYCLOADDITIONS
POLYCYCLIC ETHERS
GAMMA-ADDITIONS
spellingShingle Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
ELECTRON-DEFICIENT OLEFINS
ALPHA-AMINO-ACID
NATURAL-PRODUCTS
ALPHA,BETA-UNSATURATED IMINES
FUNCTIONALIZED CYCLOPENTENES
ASYMMETRIC-SYNTHESIS
POLYKETIDE SYNTHASE
3+2 CYCLOADDITIONS
POLYCYCLIC ETHERS
GAMMA-ADDITIONS
Jin, Zhichao
Ni, Huanzhen
Zhou, Bo
Zheng, Wenrui
Yixin, Lu
Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
description 10.1021/acs.orglett.8b02519
author2 DEPT OF CHEMISTRY
author_facet DEPT OF CHEMISTRY
Jin, Zhichao
Ni, Huanzhen
Zhou, Bo
Zheng, Wenrui
Yixin, Lu
format Article
author Jin, Zhichao
Ni, Huanzhen
Zhou, Bo
Zheng, Wenrui
Yixin, Lu
author_sort Jin, Zhichao
title Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
title_short Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
title_full Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
title_fullStr Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
title_full_unstemmed Phosphine-Catalyzed Formal Oxa-[4+2] Annulation Employing Nitroethylene and Enones: Enantioselective Synthesis of Dihydropyrans
title_sort phosphine-catalyzed formal oxa-[4+2] annulation employing nitroethylene and enones: enantioselective synthesis of dihydropyrans
publisher AMER CHEMICAL SOC
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/170220
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