Organocatalytic Asymmetric Michael-Hemiacetalization Reaction Between 2-Hydroxyacetophenones and Enals: A Route to Chiral β,γ-Disubstituted γ-Butyrolactones-Reference-Cited by-同舟云学术

Organocatalytic Asymmetric Michael-Hemiacetalization Reaction Between 2-Hydroxyacetophenones and Enals: A Route to Chiral β,γ-Disubstituted γ-Butyrolactones

Published:2017-06-02 Issue:12 Volume:82 Page:6409-6416
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Balha Megha¹,Mondal Buddhadeb¹,Sahoo Subas Chandra¹,Pan Subhas Chandra¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Guwahati, North Guwahati, Assam 781039, India

Funder

Department of Science and Technology, Ministry of Science and Technology

Max-Planck-Gesellschaft

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00363

Reference50 articles.

1. 2?-Nitro-2?-propen-1?-yl 2,2-Dimethylpropanoate (NPP), A Multiple Coupling Reagent

2. Comprehensive Enantioselective Organocatalysis

3. Asymmetric Aldol Reaction via a Dinuclear Zinc Catalyst: α-Hydroxyketones as Donors

4. A Heterodinuclear Asymmetric Catalyst for Conjugate Additions of α-Hydroxyketones to β-Substituted Nitroalkenes

5. Direct Catalytic Asymmetric Aldol Reaction: Synthesis of Either syn- or anti-α,β-Dihydroxy Ketones

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