Designing organic syntheses - Warren.pdf - Organic synthesis - ziolek6661

Designing Organic

Syntheses

A Programmed Introduction

to the

Synthon Approach

STUART WARREN

University Chemical Laboratory

Cambridge

JOHN WILEY & SONS

Chichester . New York . Brisbane . Toronto

CONTENTS

What Do You Need to Know before you Start? ........................................... 1

How to Use the Programme ......................................................................... 2

Why Bother with Disconnections? ................................................................ 2

Glossary ....................................................................................................... 4

A. INTRODUCTION TO DISCONNECTIONS, ................................... 4

frames 1-9.

B. ONE-GROUP DISCONNECTIONS, ............................................... 6

frames 10-83.

1. Disconnections of Simple Alcohols, frames 10-22.

2. Compounds Derived from Alcohols, frames 23-27.

3. Review Problems 1-3, frames 28-35.

4. Disconnections of Simple Olefins, frames 36-43.

5. Disconnections of Aryl Ketones, frames 44-48.

6. Control, frames 49-60.

7. Disconnections of Simple Ketones and Acids, frames 61-72.

8. Summary and Revision, frames 73-77.

9. Review Problems 4-6, frames 78-83.

C. TWO-GROUP DISCONNECTIONS, ................................................. 27

frames 84-130.

1. 1,3-Dioxygenated Skeletons, frames 84-111.

(a) β-Hydroxy Carbonyl Compounds, frames 84-87.

(b) α,β-Unsaturated Carbonyl Compounds, frames 88-93.

(d) Review Problems 7-8, frames 108-111.

2. 1,5-Dicarbonyl Compounds, frames 112-124.

(a) Use of the Mannich Reaction, frames 122-124.

3. Review Problems 9-11, frames 125-130.

D. ‘ILLOGICAL’ TWO GROUP DISCONNECTIONS, ......................... 42

frames 131-209

1. The 1,2-Dioxygenation Pattern, frames 131-170.

(a) α-Hydroxy Carbonyl Compounds, frames 131-149.

(b) 1,2-Diols, frames 150-157.

(d) Review Problems 12-13, frames 167-170.

2. The 1,4-Dioxygenation Pattern, frames 171-193.

(a) 1,4-Dicarbonyl Compounds, frames 171-178.

(b) γ-Hydroxy Carbonyl Compounds, frames 179-186.

(d) Review Problems 14-15, frames 190-193.

3. 1,6-Dicarbonyl Compounds, frames 194-202.

4. Review Section: Synthesis of Lactones, Review Problems 16-18,

frames 203-209.

E. GENERAL REVIEW PROBLEMS .................................................... 66

Review Problems 19-23, frames 210-219.

F. PERICYCLIC REACTIONS, .............................................................. 69

frames 220-233.

Review Problem 24, frames 232-233.

G. HETEROATOMS AND HETEROCYCLIC COMPOUNDS, ............. 74

frames 234-272.

1. Heteroatoms; Ethers and Amines, frames 234-247.

2. Heterocyclic Compounds, frames 248-264.

3. Amino Acids, frames 265-266.

4. Review Problems 25-27, frames 267-272.

H. SPECIAL METHODS FOR SMALL RINGS:

3- AND 4-MEMBERED RINGS, ......................................................... 88

1. Three-Membered Rings, frames 273-288.

2. Four-Membered Rings, frames 289-294.

3. Review Problems 28-30, frames 295-300.

I. GENERAL REVIEW PROBLEMS, ....................................................... 98

Review Problems 31-34, frames 301-308.

J. STRATEGY, ........................................................................................... 101

frames 309-390.

1. Convergent Syntheses, frames 309-318.

2. Strategic Devices.

(a) C-Heteroatom Bonds, frames 319-328.

(b) Polycyclic Compounds:

The Common Atom Approach, frames 329-333.

3. Considering All Possible Disconnections, frames 334-348.

4. Alternative FGI’s Before Disconnection - The Cost of a Synthesis,

frames 349-354.

5. Features Which Dominate Strategy, frames 355-370.

6. Functional Group Addition, frames 371-383.

(a) Strategy of Satyrated Hydrocarbon Synthesis,

frames 371-380.

(b) FGA to Intermediates, frames 381-383.

7. Molecules with Unrelated Functional Groups, frames 384-390.

K. FURTHER STUDY, .................................................................................. 124

frames 391.

L. REVISION PROBLEMS, 1-10. ................................................................ 125

frames 392-411.

M. PROBLEMS IN STRATEGY, 1-7. ........................................................ 133

frames 412-419.

N. PROBLEMS WITH SEVERAL PUBLISHED SOLUTIONS, ................ 135

frames 420-424.

WHAT DO YOU NEED TO KNOW BEFORE YOU START?

Though the programme may introduce you to some new reactions, its main aim is to

euggest an analytical approach to the design of syntheses. You therefore need to have a

reasonable grounding in organic chemistry so that you are familiar with most basic organic

reactions and can draw out their mechanisms. If you are a third year univeraity student, a

graduate, or someone with experiencc of organic chemistry in practice you will probably be

able to work straight through the programme to learn the approach and not need to learn any

new material. If you are a second year university student or someone with a limited

knowledge of organic reactions you may find you need to learn some reactions as you go

along. I have given references to these books to help you:

‘The Carbonyl Programme’:

“Chemistry of the Carbonyl Group, A Programmed Approach to Organic Reaction Mechanisms”, Stuart

Warren, Wiley 1974. This programme leads up to the present one.

‘Fleming’:

“Selected Organic Syntheses”, Ian Fleming, Wiley 1973. Synthesis from the other side: notable examples of

organic syntheses carefully explained in detail.

‘Tedder’:

“Basic Organic Chemistry”, J. M. Tedder, A. Nechvatal, and others, Wiley, 5 volumes 1966-1976. A

complete textbook of organic chemistry. Explains all the reactions used in the programme and describes many

syntheses in detail.

'Norman':

"Principles of Organic Synthesis", R. 0. C. Norman, Methuen, 1968: A taxtbook of organic chemistry from

the point of view of synthesis. An excellent source book for all the reactions used in this programme.

Whoever you are, you will certainly find discussion with your fellow students one way

to get the most out of the programme and you may well find it is a good idea to work on the

more difficult problems together. The review problems, revision problems, and problems

without worked solutions are ideal for this. In some cases I have given references to the

original literature so that you can find out more details of the various possible approaches

for yourself if you want to. It isn't necessary to look up any of these references as you work

through the programme.

HOW TO USE THE PROGRAMME

The point of programmed learning is that you learn at your own pace and that you

yourself check on your own progress. I shall give you information and ideas in chunks

called frames, each numbered and separated by a black line. Most frames contain a

question, sometimes followed by a comment or clue, and always by the answer. You must

WRITE DOWN on a piece of paper your answer to each question. You'll find that you

discover as you do so whether you really see what is being explained or not. If you simply

say to yourself 'Oh, I can do that, I don't need to write it down', and look at the answers,

you're missing the opportunity to check on your own progress as well as probably deceiving

yourself.

When you are ready to start, cover the first page with a card and pull it down to reveal

the first frame. Read and act on that frame, then reveal frame 2 and so on. If you are

unfamiliar with the disconnection approach, I suggest you read the introduction 'Wby

bother with disconnections' so that you can see what I'm driving at. Otherwise the first

sections of the programme may seem rather pointless.

WHY BOTHER WITH DISCONNECTIONS?

The aim of this programme is that you should learn how to design an organic synthesis

for yourself. Supposing you wanted to make this compound:

OMe

(1)

You would find that it had already been made by the route outlined on the chart on the next

page. You could then buy the starting materials (compounds 2, 3, 5, 8, and MeI ) and set to

work. But supposing 1 had never been synthesised. How would you design a synthesis for

it? You don't know the starting materials - all you know is the structure of the molecule you

want - the TARGET MOLECULE. Obviously you have to start with this structure and work

backwards. The key to the problem is the FUNCTIONAL GROUPS in the target molecule,

in this case the nitrogen atom, the carbonyl group, the double bond and the benzene ring

with its methoxyl group. You should learn from the programme that for most functional

groups there are one or more good DISCONNECTIONS - that is imaginary processes, the

reverse of real chemical reactions, which break a bond in the target molecule to give us the

structure of a new compound from which the target molecule can be made.

Designing organic syntheses - Warren.pdf

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