Iodine(V) Reagents in Organic Synthesis. Part 3. New Routes to Heterocyclic Compounds via o-Iodoxybenzoic Acid-Mediated Cyclizations: Generality, Scope, and Mechanism-Reference-Cited by-同舟云学术

Iodine(V) Reagents in Organic Synthesis. Part 3. New Routes to Heterocyclic Compounds via o-Iodoxybenzoic Acid-Mediated Cyclizations: Generality, Scope, and Mechanism

Published:2002-02-16 Issue:10 Volume:124 Page:2233-2244
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nicolaou K. C.¹,Baran P. S.¹,Zhong Y.-L.¹,Barluenga S.¹,Hunt K. W.¹,Kranich R.¹,Vega J. A.¹

Affiliation:

1. Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, and Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja012126h

Reference40 articles.

1. Total Synthesis of the CP Molecules CP-263,114 and CP-225,917— Part 1: Synthesis of Key Intermediates and Intelligence Gathering

2. Total Synthesis of the CP Molecules CP-225,917 and CP-263,114— Part 2: Evolution of the Final Strategy

3. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones

4. A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species

5. Acceleration of the Dess-Martin Oxidation by Water

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