Role of the Nozaki–Hiyama–Takai–Kishi Reaction in the Synthesis of Natural Products-Reference-Cited by-同舟云学术

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Role of the Nozaki–Hiyama–Takai–Kishi Reaction in the Synthesis of Natural Products

Published:2017-06-19 Issue:12 Volume:117 Page:8420-8446
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Gil Alejandro¹²^ORCID,Albericio Fernando¹²³^ORCID,Álvarez Mercedes¹²^ORCID

Affiliation:

1. ChemBio Lab, Barcelona Science Park, Baldiri Reixac 10, E-08028 Barcelona, Spain

2. CIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, Barcelona Science Park, Baldiri Reixac 10, 08028 Barcelona, Spain

3. University of Kwa-Zulu-Natal, 4001, Durban, South Africa

Funder

European Regional Development Fund

Ministerio de Econom?a y Competitividad

Generalitat de Catalunya

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.7b00144

Reference213 articles.

1. Grignard-type carbonyl addition of allyl halides by means of chromous salt. A chemospecific synthesis of homoallyl alcohols

2. Chromium(II) mediated threo selective synthesis of homoallyl alcohols

3. Highly Selective Carbon-Carbon Bond Forming Reactions Mediated by Chromium(II) Reagents

4. Selective grignard-type carbonyl addition of alkenyl halides mediated by chromium(II) chloride

5. Catalytic effect of nickel(II) chloride and palladium(II) acetate on chromium(II)-mediated coupling reaction of iodo olefins with aldehydes

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2. Enantioselective Total Synthesis of (−)-Cyathin B₂: A Desymmetric Double-Allylboration Approach;Journal of the American Chemical Society;2024-08-28

3. Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis;Angewandte Chemie International Edition;2024-08-08

4. Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis;Angewandte Chemie;2024-08-08

5. Asymmetric synthesis of the fully functionalized cyclodecene core of naturally occurring sesquiterpene hypocoprins A-C;Tetrahedron;2024-08

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