Domino Reactions in Organic Synthesis by Lutz F. Tietze, Hubertus P. Bell, Gordon Brasche

By Lutz F. Tietze, Hubertus P. Bell, Gordon Brasche

Domino reactions assist you to construct complicated buildings in one-pot reactions with no the necessity to isolate intermediates—a dream comes real. during this e-book, the well-respected professional, Professor Lutz Tietze, summarizes the chances of this response type—an process for an efficiant, economically benificial and ecological benign synthesis.
A yes needs to for each natural chemist.

Show description

Read or Download Domino Reactions in Organic Synthesis PDF

Similar organic chemistry books

March's Advanced Organic Chemistry (6th Edition)

A textbook meant for faculty seniors and graduate scholars taking a year-long path in complicated natural chemistry. this can be a vector PDF replica. Grayscale, 2379 pages. first-class caliber, with bookmarks and renumbered pages.

The 6th variation of a vintage in natural chemistry keeps its culture of excellence Now in its 6th version, March's complex natural Chemistry is still the most advantageous in natural chemistry. all through its six variants, scholars and chemists from world wide have depended on it as a necessary source for making plans and executing artificial reactions.
The 6th variation brings the textual content thoroughly present with the newest natural reactions. moreover, the references were up-to-date to allow readers to discover the newest fundamental and evaluation literature very easily.
New positive factors comprise: <LI> greater than 25,000 references to the literature to facilitate extra learn <LI> Revised mechanisms, the place required, that designate options in transparent smooth phrases <LI> Revisions and updates to every bankruptcy to carry all of them absolutely modern with the most recent reactions and discoveries <LI> A revised Appendix B to facilitate correlating bankruptcy sections with artificial adjustments

Schaum's Outline of Organic Chemistry (4th Edition) (Schaum's Outlines Series)

Tough attempt Questions? neglected Lectures? no longer adequate Time?

thankfully for you, there's Schaum's Outlines. greater than forty million scholars have relied on Schaum's to assist them reach the study room and on tests. Schaum's is the foremost to quicker studying and better grades in each topic. each one define offers all of the crucial path info in an easy-to-follow, topic-by-topic layout. you furthermore mght get hundreds and hundreds of examples, solved difficulties, and perform routines to check your abilities.
This Schaum's define delivers: * perform issues of complete motives that make stronger wisdom * insurance of the main up to date advancements on your path box * In-depth assessment of practices and purposes
totally suitable along with your lecture room textual content, Schaum's highlights all of the vital evidence you want to be aware of. Use Schaum's to shorten your examine time-and get your most sensible try ratings!
Schaum's Outlines-Problem Solved.

Solutions Manual to Accompany Organic Chemistry

The answer guide presents step by step options guiding the coed in the course of the reasoning at the back of each one challenge within the textual content. there's additionally a self-test on the finish of every bankruptcy, designed to evaluate the student's mastery of the cloth.

Additional resources for Domino Reactions in Organic Synthesis

Example text

García-Rodríguez, S. García-Granda, Angew. Chem. Int. Ed. 1998, 37, 3136− 3139. 38 D. Basavaiah, T. Satyanarayana, Chem. Commun. 2004, 32−33. 39 G. Bose, E. Ullah, P. Langer, Chem. Eur. J. 2004, 10, 6015−6028. 40 J. A. González-Vera, M. T. García-López, R. Herranz, Org. Lett. 2004, 6, 2641− 2644. 41 F. E. McDonald, F. Bravo, X. Wang, X. Wei, M. Toganoh, J. R. Rodríguez, B. Do, W. A. Neiwert, K. I. Hardcastle, J. Org. Chem. 2002, 67, 2515−2523. 42 A. X. Huang, Z. Xiong, E. J. Corey, J. Am. Chem.

Am. Chem. Soc. 1977, 99, 3088−3100. 21 B. Witulski, U. Bergsträßer, M. Gößmann, Tetrahedron 2000, 56, 4747−4752. 22 A. M. Bernard, E. Cadoni, A. Frongia, P. P. Piras, F. Secci, Org. Lett. 2002, 4, 2565−2567. 45 46 1 Cationic Domino Reactions 23 J. A. Bender, A. M. Arif, F. G. West, J. Am. Chem. Soc. 1999, 121, 7443−7444. 24 C. C. Browder, F. P. Marmsäter, F. G. West, Org. Lett. 2001, 3, 3033−3035. : V. : M. Suffness), CRC Press, Boca Raton, 1995; (c) K. C. -M. Dai, R. K. Guy, Angew. Chem. Int. Ed.

M. Arif, F. G. West, J. Am. Chem. Soc. 1999, 121, 7443−7444. 24 C. C. Browder, F. P. Marmsäter, F. G. West, Org. Lett. 2001, 3, 3033−3035. : V. : M. Suffness), CRC Press, Boca Raton, 1995; (c) K. C. -M. Dai, R. K. Guy, Angew. Chem. Int. Ed. 1994, 33, 15−44; (d) G. I. George, T. T. Chen, I. Ojima, D. M. Vyas, Taxane Anticancer Agents, American Cancer Society, San Diego, 1995. 26 (a) K. C. Nicolaou, Z. Yang, J. J. Liu, H. Ueno, P. G. Nantermet. R. K. Guy, C. F. Claiborne, J. Renaud E. A. Couladouros, K.

Download PDF sample

Rated 4.69 of 5 – based on 13 votes