Progress in Heterocyclic Chemistry: Volume 34

Progress in Heterocyclic Chemistry: Volume 34, the latest in this annual review series commissioned by the International Society of Heterocyclic Chemistry (ISHC), contains both highlights of the previous year's literature on heterocyclic chemistry and articles on new developing topics of particular interest to heterocyclic chemists. Highlight chapters in Volume 34 are all written by leading researchers in their field, thus constituting a systematic survey of the important original material reported in the literature of heterocyclic chemistry in 2021.

As with previous volumes in the series, Volume 34 will enable academic and industrial chemists and advanced students to keep abreast of developments in heterocyclic chemistry in a convenient way.

Autorentext

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.

Klappentext

Progress in Heterocyclic Chemistry: Volume 34, the latest in this annual review series commissioned by the International Society of Heterocyclic Chemistry (ISHC), contains both highlights of the previous year's literature on heterocyclic chemistry and articles on new developing topics of particular interest to heterocyclic chemists. Highlight chapters in Volume 34 are all written by leading researchers in their field, thus constituting a systematic survey of the important original material reported in the literature of heterocyclic chemistry in 2021.

As with previous volumes in the series, Volume 34 will enable academic and industrial chemists and advanced students to keep abreast of developments in heterocyclic chemistry in a convenient way.

Inhalt

1. Sulfur monoxide: generation, trapping, and synthetic applications

   Connor Prior, Richard S. Grainger

   2. Syntheses of linear azapentacenes

   Georgia A. Zissimou, Panayiotis A. Koutentis

   3. Three-membered ring systems

   Jonathon S. Russel

   4. Four-membered ring systems

   Josefa Anaya, Ramón M. Sánchez

   5.1 Five-membered ring systems: thiophenes and selenium/tellurium analogs and benzo analogs

   John A. Joule

   5.2 Five-membered ring systems: pyrroles and benzo analogs

   Justin M. Lopchuk

   5.3 Five-membered ring systems: furans and benzofurans

   Halina Kwiecien

   5.4 Five-membered ring systems: with more than one N atom

   Larry Yet

   5.5 Five-membered ring systems: with N and S atom

   Narendra B. Ambhaikar, Shriharsha Uppaluri

   5.6 Five-membered ring systems: with O and S (Se, Te) atoms

   R. Alan Aitken, Fiona M. Fotherby

   5.7 Five-membered ring systems with O and N atoms

   Franca M. Cordero, Luisa Lascialfari, Fabrizio Machetti

   6.1 Six-membered ring systems: pyridines and benzo derivatives

   Jeanese C. Badenock

   6.2 Six-membered ring systems: diazines and benzo derivatives

   K. Alison Rinderspacher

   6.3 Triazines, tetrazines, and fused ring polyaza systems

   R. Alan Aitken, Fiona M. Fotherby

   6.4 Six-membered ring systems: with O and/or S atoms

   Clementina M.M. Santos, Artur M.S. Silva

   7 Seven-membered rings

   Alex C. Bissember, Steven M. Wales, Bill C. Hawkins, Jack L.-Y. Chen, Wade F. Petersen, Andrew J. Tague, Cassandra L. Fleming, Andrew P. Cording, Ashlyn D. Bhana, Mark D. Johnstone, James P. Shephard

   8 Eight-membered and larger rings

   Charles N. Moorefield, George R. Newkome