Copper‐Catalyzed Azide–Ynamide Cyclization to Generate α‐Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N‐Heterocycles

Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycl...

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Published inAngewandte Chemie International Edition Vol. 59; no. 41; pp. 17984 - 17990
Main Authors Liu, Xin, Wang, Ze‐Shu, Zhai, Tong‐Yi, Luo, Chen, Zhang, Yi‐Ping, Chen, Yang‐Bo, Deng, Chao, Liu, Rai‐Shung, Ye, Long‐Wu
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 05.10.2020
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Abstract Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. An efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is disclosed, enabling divergent synthesis of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities, representing the first generation of α‐imino copper carbenes directly from alkynes. The asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities.
AbstractList Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first generation of α-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first generation of α-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.
Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations. An efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is disclosed, enabling divergent synthesis of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities, representing the first generation of α‐imino copper carbenes directly from alkynes. The asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities.
Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first generation of α‐imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N‐heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide–ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX‐Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide–alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.
Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via alpha-imino copper carbene intermediates is reported, representing the first generation of alpha-imino copper carbenes from alkynes. This protocol enables the practical and divergent synthesis of an array of polycyclic N-heterocycles in generally good to excellent yields with broad substrate scope and excellent diastereoselectivities. Moreover, an asymmetric azide-ynamide cyclization has been achieved with high enantioselectivities (up to 98:2 e.r.) by employing BOX-Cu complexes as chiral catalysts. Thus, this protocol constitutes the first example of an asymmetric azide-alkyne cyclization. The proposed mechanistic rationale for this cascade cyclization is further supported by theoretical calculations.
Author Wang, Ze‐Shu
Liu, Rai‐Shung
Zhai, Tong‐Yi
Chen, Yang‐Bo
Liu, Xin
Deng, Chao
Luo, Chen
Zhang, Yi‐Ping
Ye, Long‐Wu
Author_xml – sequence: 1
  givenname: Xin
  surname: Liu
  fullname: Liu, Xin
  organization: Xiamen University
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  givenname: Ze‐Shu
  surname: Wang
  fullname: Wang, Ze‐Shu
  organization: Xiamen University
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  givenname: Tong‐Yi
  surname: Zhai
  fullname: Zhai, Tong‐Yi
  organization: Xiamen University
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  givenname: Chen
  surname: Luo
  fullname: Luo, Chen
  organization: Xiamen University
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  givenname: Yi‐Ping
  surname: Zhang
  fullname: Zhang, Yi‐Ping
  organization: Xiamen University
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  givenname: Yang‐Bo
  surname: Chen
  fullname: Chen, Yang‐Bo
  organization: Xiamen University
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  surname: Deng
  fullname: Deng, Chao
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  organization: Nanjing Agricultural University
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  surname: Liu
  fullname: Liu, Rai‐Shung
  organization: National Tsing-Hua University
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  givenname: Long‐Wu
  orcidid: 0000-0003-3108-2611
  surname: Ye
  fullname: Ye, Long‐Wu
  email: longwuye@xmu.edu.cn
  organization: Chinese Academy of Sciences
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Issue 41
Keywords 2H-AZIRINES
TETHERED ALKYNES
C-H ANNULATION
alkynes
EFFICIENT SYNTHESIS
RAPID ACCESS
asymmetric catalysis
2-ALKYNYL ARYLAZIDES
CASCADE REACTION
NUCLEOPHILIC NITRENOIDS
cyclizations
CYCLOADDITION
heterocycles
copper
OXO GOLD CARBENES
Language English
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Notes Dedicated to the 70th anniversary of Shanghai Institute of Organic Chemistry
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Snippet Here an efficient copper‐catalyzed cascade cyclization of azide‐ynamides via α‐imino copper carbene intermediates is reported, representing the first...
Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via alpha-imino copper carbene intermediates is reported, representing the first...
Here an efficient copper-catalyzed cascade cyclization of azide-ynamides via α-imino copper carbene intermediates is reported, representing the first...
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SubjectTerms Alkynes
asymmetric catalysis
Asymmetry
Carbenes
Catalysts
Chemistry
Chemistry, Multidisciplinary
Copper
cyclizations
Divergence
Enantiomers
heterocycles
Intermediates
Physical Sciences
Science & Technology
Substrates
Title Copper‐Catalyzed Azide–Ynamide Cyclization to Generate α‐Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N‐Heterocycles
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202007206
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Volume 59
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