Holdings: Organotin chemistry

Organotin chemistry:

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Bibliographic Details
Main Author:	Davies, Alwyn G. (Author)
Format:	Book
Language:	German
Published:	Weinheim Wiley-VCH 2004
Edition:	2., completely rev. and updated ed.
Subjects:	Zinnorganische Verbindungen
Online Access:	Inhaltsverzeichnis
Item Description:	Literaturangaben
Physical Description:	XI, 426 S. graph. Darst. 1 CD-ROM
ISBN:	3527310231

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adam_text	* * * * * * * * * * * * * **** 1.2 1.3 1.4 1.5 2 * 2.1 2.1.1 2 . 1 . 2 2.1.3 2 . 1 . 4 2 . 1 . 5 2.2 3 * 3.1 3.1.1 3.1.2 3.1.2.1 3 . ] . 2 . 2 * 3.] .2. 3* 3.1.2.4 3.2 3.2.1 3.2.2 4 * 4.1 4 . 2 4.3 4.4 4.5 4.6 4 . 7 5 * 5.1 5 . 2 5 . 3 5.3.1 I N T R O D U C T I O N I * H I S T O R Y I * N O M E N C L A T U R E 3 * O V E R V I E W O F S Y N T H E S I S 4 * O V E R V I E W O F S T R U C T U R E S 6 * B I B L I O G R A P H Y 8 * P H Y S I C A L M E T H O D S A N D P H Y S I C A L D A T A 13* P H Y S I C A L M E T H O D S 13* I N F R A R E D A N D R A M A N S P E C T R O S C O P Y 13* M OE S S B A U E R S P E C T R O S C O P Y 14* M A S S S P E C T R O M E T R Y 16* N M R S P E C T R O S C O P Y 18* P H O T O E L E C T R O N S P E C T R O S C O P Y 2 5 * P H Y S I C A L D A T A 26* T H E S T A N N Y L G R O U P A S A S U B S T I T U E N T 31* T I N A S A H Y D R O G E N E Q U I V A L E N T 31* C H E M I C A L R E A C T I O N S 3 5 * C - S N H Y P E R C O N J U G A T I O N 3 6 * C A R B O N R A D I C A L S 3 6 * C A R B O N C A T I O N S : T H E SS- T I N E F F E C T 3 6 * F I L L E D N - S Y S T E M S 3 9 * C A R B O N C A T I O N S : T H E Y-, 8 - , A N D E - E F F E C T S 41* S T A N N Y L S U B S T I T U E N T C O N S T A N T S 41* E L E C T R O N I C E F F E C T S 41* S T E R I C E F F E C T S 4 2 * F O R M A T I O N O F T H E C A R B O N - T I N B O N D 45* T H E R E A C T I O N O F O R G A N O M E T A L L I C R E A G E N T S W I T H T I N C O M P O U N D S 45* T H E R E A C T I O N O F S T A N N Y L M E T A L L I C C O M P O U N D S W I T H O R G A N I C * E L E C T R O P H I L E S 49* T H E R E A C T I O N O F T I N O R T I N ( I 1 ) C O M P O U N D S W I T H A L K Y L H A L I D E S 51* T H E H Y D R O S T A N N A T I O N O F A L K E N E S A N D A L K Y N E S 54* M E T A L L O S T A N N A T I O N O F A L K E N E S A N D A L K Y N E S 5 9 * T H E R E A C T I O N O F A C I D I C H Y D R O C A R B O N S W I T H S N - O A N D S N - N B O N D E D * C O M P O U N D S 60* C A R B O N Y L - F O R M I N G E L I M I N A T I O N S 61* A L K Y L S T A N N A N E S 67* S T R U C T U R E S A N D P R O P E R T I E S 67* M E C H A N I S M S O F C L E A V A G E 7 0 * R E A C T I O N S 72* W I T H P R O T I C A C I D S 72* ORGANA/IN CHEMISTRY. A L W Y N G. D A V ; E S C O P Y R I G H T 2 0 0 3 W 1 L E Y - V C H V E R L A G G M B H & C O . K G A A , W E I N H E ; M ISBN 3 - 5 2 7 - 3 1 0 2 3 - 1 V 1 L L CONTENTS 5 . 3 . 2 W I T H H A L O G E N S 73* 5.3.3 W I T H L E W I S A C I D S 74* 5 . 3 . 4 W I T H S U L F U R D I O X I D E 75* 5.3.5 T I N / L I T H I U M T R A N S M E T A L L A T I O N 75* 5 . 3 . 6 W I T H F R E E R A D I C A L S 75* 5 . 3 . 7 BY E L E C T R O N T R A N S F E R 76* 5.3.8 W I T H P E R O X I D E S 78* 5.4 F L U O R O U S A1KY1STANNANES 78* 6 F U N C T I O N A L L Y - S U B S T I T U T E D A L K Y L S T A N N A N E S 82* 6.1 A - H A 1 O G E N O A 1 K Y L S T A N N A N E S 82* 6 . 2 O T H E R A - S U B S T I T U T E D A1KYLSTANNANES 84* 6.3 SS- FUNCTIONA1 A1KY L S T A N N A N E S 92* 6 . 4 Y - F U N C T I O N A L A1KY1STANNANES 94* 7 A R Y L - A N D H E T E R O A R Y L - S T A N N A N E S 100* 7.1 ARY1STANNANES 100* 7.2 T H E S T A N N Y L I U M [ON A N D THE WHE1AND [ N T E R M E D I A T E 105* 7.3 H E T E R O A R Y 1 S T A N N A N E S 107* 8 A L K E N Y L - A N D A L K Y N Y L - S T A N N A N E S , A N D S T A N N A C Y C L O P E N T A D I E N E S 114* 8.1 A1KENYL-TIN C O M P O U N D S 114* 8.1.1 F O R M A T I O N 114* 8 . 1 . 2 R E A C T I O N S 121* 8.2 A L K Y N Y L T I N C O M P O U N D S 123* 8.2.1 F O R M A T I O N 123* 8.2.2 R E A C T I O N S 125* 8.3 S T A N N A C Y C 1 0 P E N T A D I E N E S 128* 9 A L L Y L - , A L L E N Y L - , P R O P A R G Y L , A N D C Y C L O P E N T A D I E N Y L - S T A N N A N E S 133* 9.1 A L L Y L S T A N N A N E S 133* 9.1.1 F O R M A T I O N 133* 9 . 1 . 2 P R O P E R T I E S 135* 9 . 1 . 3 R E A C T I O N S 136* 9.1.3.1 T R A N S M E T A L L A T I O N S 136* 9 . 1 . 3 . 2 R E A C T I O N W I T H E1ECTROPHI1ES 137* 9 . 1 . 3 . 3 R E A C T I O N S W I T H R A D I C A L S 139* 9 . 1 . 3 . 4 ENE R E A C T I O N S 140* 9.2 A L L E N Y L - A N D P R O P A R G Y 1 - S T A N N A N E S 142* 9.2.1 P R E P A R A T I O N 142* 9 . 2 . 2 R E A C T I O N S 143* 9.3 C Y C L O P E N T A D I E N Y L S T A N N A N E S 144* 9.3.1 F O R M A T I O N 144* 9 . 3 . 2 P R O P E R T I E S 145* 9.3.3 R E A C T I O N S 147* 9 . 3 . 4 S T A N N Y 1 M E T A L L O C E N E S 148* 10 S T A N N A C Y C L O A L K A N E S 156* 10.1 M O N O S T A N N A C Y C L O A L K A N E S , R 2 S N ( C H 2 )11 156* 10.2 S T A N N A C Y C L O P E N T A D I E N E S 159* 10.3 O L I G O S T A N N A C Y C L O A L K A N E S , [R 2 S N ( C H 2 )I1]M 160* I X 10.3.1 10.3.2 11* 11.1 11.1.1 11.1.2 11.1.3 11.1.4 11.1.5 11.2 11.3 1104* 12* 12.1 12.1.1 12.1.2 12.2 12.3 1204* 13* 13.1 13.1.1 13.1.2 1 3 . 1 . 3 13.2 13.3 1304* 14* 14.1 14.1.1 14.1.2 14.1.3 14.2 14.2.1 14.2.2 14.3 14.3.1 14.3.2 1404* 14.5 15* 15.1 15.1.1 15.1.2 15.1.3 15.1.4 C O N T E N T S F O R M A T I O N S T R U C T U R E S A N D P R O P E R T I E S O R G A N O T I N H A L I D E S P R E P A R A T I O N T H E R E A C T I O N O F RM W I T H S N X 4 T H E K O C H E S H K O V R E A C T I O N P R E P A R A T I O N FROM O R G A N O T I N O X I D E S O R H Y D R O X I D E S E X C H A N G E O F A N I O N I C G R O U P S A T T I N T H E R E A C T I O N S O F H A L O G E N S W I T H S N - S N B O N D E D C O M P O U N D S P H Y S I C A L P R O P E R T I E S A N D S T R U C T U R E S C O O R D I N A T I O N C O M P L E X E S R E A C T I O N S O R G A N O T I N H Y D R O X I D E S A N D O X I D E S T R I O R G A N O T I N H Y D R O X I D E S AND O X I D E S P R E P A R A T I O N AND P R O P E R T I E S R E A C T I O N S D I O R G A N O T I N H Y D R O X I D E S A N D O X I D E S M O N O O R G A N O T I N H Y D R O X I D E S AND O X I D E S S T A N N A M E T A L L O X A N E S O R G A N O T I N C A R B O X Y L A T E S A N D O T H E R O X Y E S T E R S . S T A N N Y L I U M I O N S O R G A N O T I N C A R B O X Y L A T E S P R E P A R A T I O N S T R U C T U R E S P R O P E R T I E S C A R B O N A T E S A N D C A R B A M A T E S D E R I V A T I V E S O F P H O S P H O R U S A C I D S O R G A N O T I N D E R I V A T I V E S O F O T H E R O X Y A C I D S A N D O F T H I O A C I D S O R G A N O T I N A L K O X I D E S , P H E N O X I D E S , A N D P E R O X I D E S A C Y C L I C A L K O X I D E S AND P H E N O X I D E S P R E P A R A T I O N S T R U C T U R E S A N D P R O P E R T I E S R E A C T I O N S 1 , 3 , 2 - D I O X A S T A N N A C Y C L O A L K A N E S F O R M A T I O N S T R U C T U R E S A N D P R O P E R T I E S A C Y C L I C O R G A N O T I N E N O L A T E S P R E P A R A T I O N R E A C T I O N S 1 , 3 , 2 - D I O X A S T A N N O L E N E S O R G A N O T I N P E R O X I D E S O R G A N O T I N H Y D R I D E S P R E P A R A T I O N R E D U C T I O N S W I T H M E T A L H Y D R I D E S D E C A R B O X Y L A T I O N O F S T A N N Y L F O R M A T E S H Y D R O L Y S I S O F S T A N N Y L M E T A L L I C C O M P O U N D S A L K Y L A T I O N O F R 2 S N H M 160* 162* 166* 166* 166* 167* 168* 169* 170* 171* 174* 175* 179* 179* 179* 182* 185* 193* 195* 203* 203* 203* 205* 207* 208* 209* 2 1 0 * 2 1 4 * 2 1 4 * 2 1 4 * 2 1 8 * 219* 223* 2 2 3 * 2 2 4 * 2 2 8 * 229* 2 3 0 * 233* 2 3 4 * 2 4 4 * 2 4 4 * 2 4 4 * 2 4 6 * 2 4 7 * 247* X CONTENTS 15.1.5* 15.2 15.3 15.3.1 1 5 . 3 . 2 15.3.3 1 5 . 3 . 4 15.3.5 15.3.5.1 1 5 . 3 . 5 . 2 15.3.5.3 1 5 . 3 . 5 . 4 1 6 * 16.1 16.1.1 16.1.1.1 1 6 . 1 . 1 . 2 16.1.1.3 1 6 . 1 . 1 . 4 16.1.1.5 1 6 . 1 . 2 16.1.3 16.1.3.1 16.1.3.2 16.1.3.3 1 6 . 1 . 3 . 4 16.2 16.3 16.4 16.5 16.6 1 7 * 17.1 17.1.1 1 7 . 1 . 2 17.1.3 17.2 17.3 18* 18.1 18.2 18.2.1 18.2.1.1 1 8 . 2 . 1 . 2 18.2.1.3 1 8 . 2 . 1 . 4 1 8 . 2 . 1 . 5 1 8 . 2 . 1 . 6 S P E C I A L H Y D R I D E S 248* P R O P E R T I E S 249* R E A C T I O N S 251* R E A C T I O N S W I T H P R O T I C A C I D S A N D C A R B E N I U M IONS. 2 5 2 * R E A C T I O N S W I T H M E T A L H A L I D E S 253* R E A C T I O N S W I T H S T R A N G BASES 253* R E A C T I O N S L E A D I N G TO T H E F O R M A T I O N O F S N - S N B O N D S 253* RADICA1 R E A C T I O N S 255* R E A C T I O N S O F R A D I C A L S W I T H T I N H Y D R I D E S 2 5 6 * R E D U C T I O N O F H A L I D E S 257* R E D U C T I O N O F THIOCARBONY1 C O M P O U N D S 2 5 9 * R E D U C T I O N O F O T H E R S U B S T R A T E S 2 5 9 * COMPOUNDS WITH SN-N BONDS 266* A M I N O S T A N N A N E S 266* P R E P A R A T I O N 266* T R A N S M E T A L L A T I O N 266* T R A N S A M I N A T I O N 2 6 7 * A D D I T I O N TO M U L T I P L E B O N D S 268* ENE R E A C T I O N S 268* M I S C E L L A N E O U S M E T H O D S 2 6 9 * S T R U C T U R E S 269* R E A C T I O N S 270* W I T H P R O T I C A C I D S 270* W I T H M E T A L D E R I V A T I V E S 271* W I T H O T H E R S I N G L Y - B O N D E D E L E C T R O P H I L E S 2 7 2 * W I T H D O U B L Y - B O N D E D E L E C T R O P H I L E S 273* S T A N N Y L P O R P H Y R I N S A N D C O R R O L E S 274* A M I D O S T A N N A N E S 275* S U L F O N A M I D O S T A N N A N E S 276* S T A N N A I M I N E S , R 2 S N = N R 277* C O M P O U N D S W I T H S N - P B O N D S 2 7 8 * COMPOUNDS WITH SN-S BONDS 283* O R G A N O T I N S U L F I D E S 283* P R E P A R A T I O N 283* S T R U C T U R E S 285* R E A C T I O N S 286* S T A N N A T H I O N E S R 2 SN=S 287* O R G A N O T I N T H I O L A T E S R SN(SR )4_ 287* COMPOUNDS WITH SN-SN BONDS 292* 1 N T R O D U C T I O N 292* A C Y C L I C D I S T A N N A N E S 292* F O R M A T I O N 292* F R O M A S T A N N Y L M E T A L L I C C O M P O U N D A N D A H A L I D E R SNX 4 _ 2 9 2 * F R O M AN O R G A N O T I N C O M P O U N D R SNX 4_ A N D A M E T A L 293* F R O M AN O R G A N O T I N H Y D R I D E R SNH 4 _ A N D A C O M P O U N D R N SNX4_ N 294* BY E L I M I N A T I O N O F D I H Y D R O G E N FROM AN O R G A N O T I N H Y D R I D E 295* BY I N S E R T I O N O F A S T A N N Y L E N E R 2 S N : INTO AN SNM B O N D 296* BY A B S T R A C T I O N O F A H Y D R O G E N A T O M F R O M R 3 SNH 296* 18.2.1.7 1 8 . 2 . 2 18.2.3 18.3 18.4 19* 19.1 19.1.1 19.1.2 19.1.3 19.1.4 19.1.5 19.2 19.3 19.4 19.5 19.6 19.7 19.8 19.9 20* 20.1 20.1.1 2 0 . 1 . 2 2 0 . 1 . 3 2 0 . 2 20.3 20.4 21* 21.1 21.1.1 2 1 . 1 . 2 2 1 . 2 21.3 2 1 . 4 21.5 22* 22.1 22.2 22.3 2 3 * 23.1 2 3 . 2 23.3 BY C A T H O D I C R E D U C T I O N O F R 3 S N X S T R U C T U R E S P R O P E R T I E S L I N E A R O L I G O S T A N N A N E S C Y C L I C O L I G O S T A N N A N E S C O M P O U N D S W I T H T I N - M E T A L B O N D S A L K A L I M E T A L S F O R M A T I O N P R O P E R T I E S S T R U C T U R E S R E A C T I O N S P E N T A O R G A N O S T A N N A T E S RSSN - L T M A G N E S I U M C A L C I U M , S T R O N T I U M , A N D B A R I U M B O R O N A N D A L U M I N I U M S I L I C O N , G E R M A N I U M , A N D L E A D C O P P E R Z I N C , C A D M I U M , A N D M E R C U R Y P L A T I N U M A N D P A L L A D I U M O T H E R T R A N S I T I O N M E T A L S O R G A N O T I N R A D I C A L S A N D R A D I C A L I O N S O R G A N O T I N R A D I C A L S R 3 S N * G E N E R A T I O N * E S R S P E C T R A * R E A C T I O N S * S T A N N Y L A L K Y L R A D I C A L S R 3 SNC,, * R A D I C A L C A T I O N S R S N X 4 _ + * I L 1 L R A D I C A L A N I O N S R SNX 4 _ 1 L - A N D R 2 S N - S T A N N Y L E N E S , D I S T A N N E N E S , A N D S T A N N E N E S ( J - B O N D E D S T A N N Y L E N E S T R A N S I E N T S T A N N Y L E N E S P E R S I S T E N T S T A N N Y L E N E S D I S T A N N E N E S D I S T A N N Y N E S S T A N N E N E S A N D H E T E R O S T A N N E N E S N - B O N D E D S T A N N Y L E N E S O R G A N I C S Y N T H E S I S : T I N / L I T H I U M T R A N S M E T A L L A T I O N , T H E S T I L L E R E A C T I O N , A N D T H E R E M O V A L O F T I N R E S I D U E S T I N / L I T H I U M T R A N S M E T A L L A T I O N S T I L L E C O U P L I N G R E A C T I O N S T H E R E M O V A L O F T I N R E S I D U E S A P P L I C A T I O N S , E N V I R O N M E N T A L I S S U E S , A N D A N A L Y S I S A P P L I C A T I O N S E N V I R O N M E N T A L I S S U E S A N A L Y S I S A U T H O R I N D E X S U B J E C T I N D E X CONTENTS X I 2 9 6 * 2 9 7 * 2 9 7 * 301* 3 0 3 * 311* 311* 311* 3 1 3 * 3 1 3 * 3 1 4 * 3 1 5 * 3 1 6 * 317* 3 1 7 * 3 1 9 * 321* 322* 3 2 3 * 3 2 7 * 3 3 3 * 3 3 3 * 333* 3 3 8 * 3 3 9 * 3 4 3 * 3 4 4 * 3 4 6 * 351* 351* 351* 3 5 3 * 3 5 9 * 3 6 0 * 361* 3 6 3 * 3 7 3 * 373* 3 7 5 * 3 7 8 * 3 8 3 * 3 8 3 * 3 8 7 * 3 8 8 * 391* 421*
any_adam_object	1
author	Davies, Alwyn G.
author_facet	Davies, Alwyn G.
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author_sort	Davies, Alwyn G.
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callnumber-subject	QD - Chemistry
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classification_tum	CHE 630f CHE 330f CHE 365f
ctrlnum	(OCoLC)249015435 (DE-599)BVBBV019318820
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dewey-hundreds	500 - Natural sciences and mathematics
dewey-ones	547 - Organic chemistry
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edition	2., completely rev. and updated ed.
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id	DE-604.BV019318820
illustrated	Illustrated
indexdate	2024-07-09T19:57:33Z
institution	BVB
isbn	3527310231
language	German
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-012786228
oclc_num	249015435
open_access_boolean
owner	DE-91G DE-BY-TUM DE-19 DE-BY-UBM DE-703 DE-29T DE-11
owner_facet	DE-91G DE-BY-TUM DE-19 DE-BY-UBM DE-703 DE-29T DE-11
physical	XI, 426 S. graph. Darst. 1 CD-ROM
publishDate	2004
publishDateSearch	2004
publishDateSort	2004
publisher	Wiley-VCH
record_format	marc
spelling	Davies, Alwyn G. Verfasser aut Organotin chemistry Alwyn G. Davies 2., completely rev. and updated ed. Weinheim Wiley-VCH 2004 XI, 426 S. graph. Darst. 1 CD-ROM txt rdacontent n rdamedia nc rdacarrier Literaturangaben Zinnorganische Verbindungen Zinnorganische Verbindungen (DE-588)4190905-7 gnd rswk-swf Zinnorganische Verbindungen (DE-588)4190905-7 s DE-604 OEBV Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=012786228&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Davies, Alwyn G. Organotin chemistry Zinnorganische Verbindungen Zinnorganische Verbindungen (DE-588)4190905-7 gnd
subject_GND	(DE-588)4190905-7
title	Organotin chemistry
title_auth	Organotin chemistry
title_exact_search	Organotin chemistry
title_full	Organotin chemistry Alwyn G. Davies
title_fullStr	Organotin chemistry Alwyn G. Davies
title_full_unstemmed	Organotin chemistry Alwyn G. Davies
title_short	Organotin chemistry
title_sort	organotin chemistry
topic	Zinnorganische Verbindungen Zinnorganische Verbindungen (DE-588)4190905-7 gnd
topic_facet	Zinnorganische Verbindungen
url	http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=012786228&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT daviesalwyng organotinchemistry

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