A Novel Strategy for the Synthesis of Molecules with Helical Chirality. Intramolecular [2 + 2 + 2] Cycloisomerization of Triynes under Cobalt Catalysis-Reference-Cited by-同舟云学术

A Novel Strategy for the Synthesis of Molecules with Helical Chirality. Intramolecular [2 + 2 + 2] Cycloisomerization of Triynes under Cobalt Catalysis

Published:1998-05-22 Issue:12 Volume:63 Page:4046-4050
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Stará Irena G.¹,Starý Ivo¹,Kollárovič Adrian¹,Teplý Filip¹,Šaman David¹,Tichý Miloš¹

Affiliation:

1. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo n. 2, 166 10 Prague 6, Czech Republic

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9801263

Reference18 articles.

1. Stereochemical Dichotomy in the Stevens Rearrangement of Axially Twisted Dihydroazepinium and Dihydrothiepinium Salts. A Novel Enantioselective Synthesis of Pentahelicene

2. Synthèses Asymétriques Potentielles Impliquant la Réaction “Ene”

3. Racemization Barriers of Helicenes: A Computational Study1

4. The First Helical-Chiral Phosphane Ligands: rac-[5]- and rac-[6]-Heliphos

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