Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds-Reference-Cited by-同舟云学术

Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds

Published:2000-07-26 Issue:32 Volume:122 Page:7847-7848
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Saito Susumu¹,Shiozawa Masahito¹,Nagahara Takashi¹,Nakadai Masakazu¹,Yamamoto Hisashi¹

Affiliation:

1. Graduate School of Engineering, Nagoya University, CREST Japan Science and Technology Corporation (JST) Furo-cho, Chikusa, Nagoya 464-8603, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja000789d

Reference3 articles.

1. Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide)

2. For the general aspects of the conformation (s-cisvss-trans) of unsaturated carbonyl compounds, see: Stereochemistry of OrganicCompounds; Eliel, E. L.; Wilen, S. H. Eds.; John Wiley & Sons: New York; 1994; Chapter 10.2., p 615. Also see the depiction below for two major conformations of an α,β-unsaturated carbonyl compound and diene, respectively. The definition for the conformations (s-transands-cis, where “s” denotes a “single bond”) of an extended dienolate is based on that for a diene.

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