Progress in Heterocyclic Chemistry

Herausgegeben:Gribble, Gordon; Joule, John A.

• Broschiertes Buch

Produktbeschreibung

Progress in Heterocyclic Chemistry, Volume 32, the latest in this annual review series commissioned by the International Society of Heterocyclic Chemistry (ISHC), highlights the previous year's literature on heterocyclic chemistry, along with articles on new developing topics of particular interest to heterocyclic chemists. Chapters highlighted in volume 32 are written by leading researchers in their field, providing a systematic survey of important, original material reported in the literature of heterocyclic chemistry in 2019. As with previous volumes in the series, this release will help academic and industrial chemists and advanced students keep abreast of developments in heterocyclic chemistry.

Produktdetails

• Progress in Heterocyclic Chemistry Volume 32
• Verlag: Elsevier / Elsevier Science & Technology
• Artikelnr. des Verlages: C2020-0-01185-0
• Englisch
• Abmessung: 31mm x 152mm x 229mm
• Gewicht: 1120g
• ISBN-13: 9780323898126
• Artikelnr.: 60412979

Autorenporträt

Gordon Gribble is the Dartmouth Professor of Chemistry at Dartmouth College, Hanover, USA. His research program covers several areas of organic chemistry, most of which involve synthesis, including novel indole chemistry, triterpenoid synthesis, DNA intercalation, and new synthetic methodology. Prof. Gribble also has a deep interest in naturally occurring organohalogen compounds and in the chemistry of wine and wine making.

John Arthur Joule did his BSc, MSc, and PhD degrees at The University of Manchester, obtaining his PhD in 1961. He then undertook post-doctoral work at Princeton University and Stanford University, before joining the academic staff of the Chemistry Department at The University of Manchester in 1963, where he is currently a Professor. In 1996 he received an RSC Medal for Heterocyclic Chemistry.

Inhaltsangabe

1. The Enantiospecific Synthesis of Indole Alkaloids which Culminated in the Ambidextrous Pictet-Spengler Reaction for the C-19 Methyl-Substituted Sarpagine Family
2. Epi-3,6-dithio-2,5-diketopiperazines (ETPs): An Overview of Synthetic Approaches to the ETP Core
3. Three-Membered Ring Systems
4. Four-Membered Ring Systems
5. Five-Membered Ring Systems
6. Six-Membered Ring Systems
7. Seven-Membered Rings
8. Eight-Membered and Larger Rings