(Q28298530)

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Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry

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Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry (English)

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author name string

S R S Saibabu Kotti

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1

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Cody Timmons

series ordinal

2

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Guigen Li

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3

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language of work or name

English

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publication date

February 2006

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published in

Chemical Biology and Drug Design

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volume

67

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issue

2

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page(s)

101-14

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cites work

Electrophilic diamination of alkenes by using FeCl(3)-PPh(3) complex as the catalyst

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https://api.crossref.org/works/10.1111%2FJ.1747-0285.2006.00347.X

retrieved

21 January 2018

N,N-Dichloro-2-nitrobenzenesulfonamide as the Electrophilic Nitrogen Source for Direct Diamination of Enones

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reference URL

https://api.crossref.org/works/10.1111%2FJ.1747-0285.2006.00347.X

retrieved

21 January 2018

Manganese (IV) oxide-catalyzed electrophilic diamination of electron-deficient alkenes provides an easy synthesis of alpha,beta-diamino acid and ketone derivatives for peptidomimetic studies.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1747-0285.2006.00347.X

retrieved

21 January 2018

A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions

1 reference

19 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1021/JA973174Y

Identifiers

DOI

10.1111/J.1747-0285.2006.00347.X

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PubMed publication ID

16492158

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ResearchGate publication ID

7285427

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(Q28298530)

Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry

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