(Z)-Selective Enol Triflation of α-Alkoxyacetoaldehydes: Application to Synthesis of (Z)-Allylic Alcohols via Cross-Coupling Reaction and [1,2]-Wittig Rearrangement-Reference-Cited by-同舟云学术

(Z)-Selective Enol Triflation of α-Alkoxyacetoaldehydes: Application to Synthesis of (Z)-Allylic Alcohols via Cross-Coupling Reaction and [1,2]-Wittig Rearrangement

Published:2015-05-22 Issue:11 Volume:80 Page:5696-5703
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kurosawa Fumiya¹,Nakano Takeo¹,Soeta Takahiro¹,Endo Kohei¹,Ukaji Yutaka¹

Affiliation:

1. Division of Material Chemistry, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00647

Reference92 articles.

1. Stereoselective Synthesis of Z-Alkenes

2. Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure (Z)-Olefins in Polyfunctionalized Bioactive Molecules?

3. Synthesis of Z-Alkenes from Rh(I)-Catalyzed Olefin Isomerization of β,γ-Unsaturated Ketones

4. Z-Selective Alkene Isomerization by High-Spin Cobalt(II) Complexes

5. Facile Synthesis of Z-Alkenes via Uphill Catalysis

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