(Q56589822)

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A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system

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A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system (English)

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Hideyo Takahashi

1

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Masato Yoshioka

series ordinal

2

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Masaji Ohno

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3

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Susumu Kobayashi

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4

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publication date

April 1992

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published in

Tetrahedron Letters

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volume

33

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issue

18

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page(s)

2575-2578

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cites work

Synthesis of cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2992246-9

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7 January 2021

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Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins

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19 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1021/JA00002A080

Asymmetric catalytic cyclopropanation of olefins: bis-oxazoline copper complexes

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19 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/S0040-4039(00)98014-6

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DOI

10.1016/S0040-4039(00)92246-9

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(Q56589822)

A catalytic enantioselective reaction using a C2-symmetric disulfonamide as a chiral ligand: cyclopropanation of allylic alcohols by the Et2Zn-CH2I2-disulfonamide system

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