Stereoselective Synthesis of 7-(E )-Arylidene-2-chloro-6-azabicyclo[3.2.1]octanes via Aluminum Chloride-Promoted Cyclization/Chlorination of Six-Membered Ring 3-Enynamides-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 7-(E )-Arylidene-2-chloro-6-azabicyclo[3.2.1]octanes via Aluminum Chloride-Promoted Cyclization/Chlorination of Six-Membered Ring 3-Enynamides

Published:2017-04-28 Issue:13 Volume:359 Page:2196-2201
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Yeh Ming-Chang P.¹,Chang Yi-Mei¹,Lin Hsin-Hui¹

Affiliation:

1. Department of Chemistry; National Taiwan Normal University; 88 Ding-Jou Road, Sec. 4 Taipei 11677 Taiwan, R.O.C.

Funder

Ministry of Science and Technology of the Republic of China

Publisher

Wiley

Subject

General Chemistry

Reference57 articles.

1. Synthesis and absolute configuration of the Aristotelia alkaloid peduncularine

2. Construction of the 6-Azabicyclo[3.2.1]octane Ring System via Higher-Order Cycloaddition; Formal Total Synthesis of (±)-Peduncularine

3. Formal Synthesis of (±)-Peduncularine: Use of the [3 + 2] Annulation of Allylic Silanes and Chlorosulfonyl Isocyanate

4. A mild new procedure for production, cyclization and trapping of amidyl radicals: application to a formal total synthesis of peduncularine

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