Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction

The addition of a carbene catalyst to an indole aryl aldehyde leads to the activation of a remote sp2 carbon that is five atoms away from the catalyst. The unsaturated Breslow intermediate formed between the catalyst and substrate undergoes an internal redox reaction and remote carbon protonation to...

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Main Authors: Zheng, Pengcheng, Wu, Shuquan, Mou, Chengli, Xue, Wei, Jin, Zhichao, Chi, Robin Yonggui
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/137753
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1377532023-02-28T19:28:14Z Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction Zheng, Pengcheng Wu, Shuquan Mou, Chengli Xue, Wei Jin, Zhichao Chi, Robin Yonggui School of Physical and Mathematical Sciences Science::Chemistry::Organic chemistry Carbene Catalyst Breslow Intermediate The addition of a carbene catalyst to an indole aryl aldehyde leads to the activation of a remote sp2 carbon that is five atoms away from the catalyst. The unsaturated Breslow intermediate formed between the catalyst and substrate undergoes an internal redox reaction and remote carbon protonation to generate an analogous azolium vinyl enolate intermediate. Subsequent [4+2] reaction with cyclic imine substrates eventually affords multicyclic pyridoindoles as nearly single diastereomers with excellent enantioselectivities. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) Accepted version 2020-04-13T07:38:04Z 2020-04-13T07:38:04Z 2019 Journal Article Zheng, P., Wu, S., Mou, C., Jin, Z., & Chi, R. Y. (2019). Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction. Organic Letters, 21(13), 5026-5029. doi:10.1021/acs.orglett.9b01624 1523-7060 https://hdl.handle.net/10356/137753 10.1021/acs.orglett.9b01624 31199655 2-s2.0-85067946714 13 21 5026 5029 en Organic Letters This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.9b01624 application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry::Organic chemistry
Carbene Catalyst
Breslow Intermediate
spellingShingle Science::Chemistry::Organic chemistry
Carbene Catalyst
Breslow Intermediate
Zheng, Pengcheng
Wu, Shuquan
Mou, Chengli
Xue, Wei
Jin, Zhichao
Chi, Robin Yonggui
Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
description The addition of a carbene catalyst to an indole aryl aldehyde leads to the activation of a remote sp2 carbon that is five atoms away from the catalyst. The unsaturated Breslow intermediate formed between the catalyst and substrate undergoes an internal redox reaction and remote carbon protonation to generate an analogous azolium vinyl enolate intermediate. Subsequent [4+2] reaction with cyclic imine substrates eventually affords multicyclic pyridoindoles as nearly single diastereomers with excellent enantioselectivities.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Zheng, Pengcheng
Wu, Shuquan
Mou, Chengli
Xue, Wei
Jin, Zhichao
Chi, Robin Yonggui
format Article
author Zheng, Pengcheng
Wu, Shuquan
Mou, Chengli
Xue, Wei
Jin, Zhichao
Chi, Robin Yonggui
author_sort Zheng, Pengcheng
title Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
title_short Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
title_full Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
title_fullStr Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
title_full_unstemmed Addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
title_sort addition of a carbene catalyst to indole aryl aldehyde activates a remote δ-sp2 carbon for protonation and formal [4+2] reaction
publishDate 2020
url https://hdl.handle.net/10356/137753
_version_ 1759853465070206976