Tandem [1,2]-Wittig Rearrangement/Lactonization of γ-Benzyloxy Vinylogous Urethanes: Application to the Synthetic Studies of Maculalactone A, Planchol C and γ-Lycorane-Reference-Cited by-同舟云学术

Tandem [1,2]-Wittig Rearrangement/Lactonization of γ-Benzyloxy Vinylogous Urethanes: Application to the Synthetic Studies of Maculalactone A, Planchol C and γ-Lycorane

Published:2017-11-30 Issue:1 Volume:7 Page:145-149
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Ho Guo-Ming¹²,Li Yu-Jang¹^ORCID

Affiliation:

1. Department of Applied Chemistry; National Chiayi University; 300 Syuefu Road Chiayi City 60004 Taiwan

2. Genomics Research Center; Academia Sinica; 128 Academia Road, Section 2 Taipei 11529 Taiwan

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Organic Chemistry

Reference80 articles.

1. [2,3]-Wittig sigmatropic rearrangements in organic synthesis

2. Acyclic Stereocontrol via [2,3]-Wittig Sigmatropic Rearrangement

3. Asymmetric [2,3]-Wittig rearrangement as a general tool for asymmetric synthesis

4. Enantioselective Synthesis by Lithiation Adjacent to Oxygen and Subsequent Rearrangement

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