Houben-Weyl methoden der organischen chemie

c9

1'74(1979)C9-Cll 0 Else~ier SequoiaS.X.,Lausanne -Prinied in The Netherlands

Jo~~rnalo~Organorrwtollic Chemistp.

HOUBEN-WEYL Volume H_

FIETHODEN

13,

Kropf,

Pawlenko, xxxii

The

editor;

volume

authors;

pages;

organic

metallic

synthesis.

The facility

with

nucleophilic hydrogen

of

in

organotins

for

some

for

tions,

however,

butyl,

octyl,

organotin synthesis

of

All the

simple

hydrides, the

greatly detailed the

is

the

organic

their as

commercial

have

the

be-

Houben-

account and

organic

of

orderly, The

large

reader

who

of

the

cleave

number

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reactions

functionality

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for

tin-

appli-

chemistry. importance

poly(viny1 which

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are

applica-

on

tin

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more

methods

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know

about

the

compounds, etc.)

equations read of

on the

is

-

recent the

these

tin,

organotin

and and

German

synthesis

presented

manner

tin-carbon

functionality

the

organotinsto

systematic

does

their

basis

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of

biocides

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carboxylates, very

the

available

need

the

electrophilic

organic and

and

reactivity

commercial

(tetraorganotin

oxides,

is- formed

availability.

simple

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spectrum

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by

applications

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1978,

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organometallic

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volume

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hydrides

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decade and

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organic

organotins

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involve

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halides,

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organic

tin-carbon

course,

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their

research

Sn;

and

Stuttgart,

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in

welcomed

well

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stabilizers

responsible

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is

in

and

in

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as

organotin

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years,

chloride)

tin

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the

it

organotins

The

Ge,

Kalinowski

alike.

reagents,

bond

cations

of

will

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which

H.-O.

reagents

series

with

Edition,

(in German).

Therefore,

chemist

4th

VERBIXDUNGEN:

B%hr,

as

compounds

ease

CHEMIE,

Georg-Thieme-Verlag,

420

useful

organometallics

organotin

G.

derivatives

organometallic

of

DM

increasingly

Weyl

ORGANISCHEN

6, METALLORGANISCHE

volume

f 599

come

of

Part

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to

discussed

tables

well.. organotins

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bonds,

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intro-

preparative

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Cl0 Particularly

of

value

organotin

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suffers

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view

synthesis type

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reaction

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nomenclature,

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end

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really

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give

synthesis

information

found

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a good,

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organotins to

in reaction

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the

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of

to

tin

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to

section of

organo-

short

a good

go

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toxicology

analysis

are

obtain

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the

the

and

appreciation

reactivity,

section

To

will

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contrast,

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these

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beginning

tin

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reader

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tables_

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Chemistry

coverage

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references

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properties

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organotin

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properties-

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organotin Handbook

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information,

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hand-

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But,

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J.

larger

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groups much

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research

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research

commercial

the

first,

years

utility

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Organogermanium reagents

world-wide

to

is given

.

book.

utility

synthesis

treatment

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us,

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organogermanium

Cl1 chemistry

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an

author

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review

articles

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organotin This

addition far to

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organic

chemistry

of

has

some

purpose

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that

organogermanium

this

book

research

doing. of

references and

adequately

which

are

which cited

a somewhat

complex

explained,

and

monographs

which

deal

are

worth

throughout compound

index,

bibliographies

with

of

organogermanium

chemistry-

outweigh the

worth

index

excellent to

to others

features

many

which,

and

volume

Hcuben-Weyl

suggest

interesting

There

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Houben-Weyl of

faults

chemist germanium

Department of Chemistry z4assachusetts Institute Cambridge, flassachusetts

all and

who

seeks

and

tin.

volume

chemistry it will an

will

be

an

libraries: be

particularly

introduction

into

Dietmar of Technology 02139 (USA)

indispensible

its

virtues useful

the

organic

Seyferth