Organic Reactions, Volume 79 | Zookal Textbooks | Zookal Textbooks
  • Author(s) Scott E. Denmark
  • Edition1
  • Published21st December 2012
  • PublisherJohn Wiley & Sons Inc (US)
  • ISBN9781118509418
Volume 79 in the venerable Organic Reactions series contains two chapters. The first addresses cross-coupling reactions of organotrifluoroborate salts, useful in the development of natural products, materials, and pharmacologically active substances. It is an excellent companion to two previous chapters on tin-based and silicon-based cross-couplings contained in Volumes 50 and 75, respectively. The second chapter addresses asymmetric transformations by deprotonation using chiral lithium amides, useful in target-oriented synthesis, and representing one of the most powerful workhorse reactions in organic synthesis.

Organic Reactions, Volume 79

Format
In stock at supplier

Leaves in 1-4 weeks

$285.39 $332.95 Save $47.56
or 4 payments of $71.34 with Zookal accepts Afterpay
Add Zookal Study FREE trial and save a further 20% 

NEW PRICE

$228.31 + free shipping

(20% off - save $57.08)

Zookal Study Free trial

14-day FREE trial. $14.95/mo after. Cancel anytime.

*Discount will apply at checkout.

 See terms and conditions

You will get a further 20% off for this item ($228.31 after discount) because you have added Zookal Study Premium Free Trial to your bag.

For this discount to apply, you will need to complete checkout with the Zookal Study Premium Free Trial in your bag.

-
+
  • Author(s) Scott E. Denmark
  • Edition1
  • Published21st December 2012
  • PublisherJohn Wiley & Sons Inc (US)
  • ISBN9781118509418
Volume 79 in the venerable Organic Reactions series contains two chapters. The first addresses cross-coupling reactions of organotrifluoroborate salts, useful in the development of natural products, materials, and pharmacologically active substances. It is an excellent companion to two previous chapters on tin-based and silicon-based cross-couplings contained in Volumes 50 and 75, respectively. The second chapter addresses asymmetric transformations by deprotonation using chiral lithium amides, useful in target-oriented synthesis, and representing one of the most powerful workhorse reactions in organic synthesis.
translation missing: en.general.search.loading