New Lewis-Acidic Molybdenum(II) and Tungsten(II) Catalysts for Intramolecular Carbonyl Ene and Prins Reactions. Reversal of the Stereoselectivity of Cyclization of Citronellal-Reference-Cited by-同舟云学术

New Lewis-Acidic Molybdenum(II) and Tungsten(II) Catalysts for Intramolecular Carbonyl Ene and Prins Reactions. Reversal of the Stereoselectivity of Cyclization of Citronellal

Published:1999-03-20 Issue:8 Volume:64 Page:2765-2775
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kočovský Pavel¹,Ahmed Ghafoor¹,Šrogl Jiří¹,Malkov Andrei V.¹,Steele John¹

Affiliation:

1. Department of Chemistry, University of Leicester, Leicester LE1 7RH, U.K., and Discovery Chemistry, Pfizer Central Research, Sandwich, Kent CT13 9NJ, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9821675

Reference88 articles.

1. Scandium trifluoromethaneslfonate, an efficient catalyst for the intermolecular carbonyl-ene reaction and the intramolecular cyclisation of citronellal

2. Stereoselective Synthesis of meso-2,6-Diaminopimelic Acid and Its Selectively Protected Derivatives

3. C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Enantioselective Catalysis of the Glyoxylate−Ene Reaction

4. A Highly Stereoselective Preparation ofl-Isopulegol

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