FI (list display)

C07C29/00	Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring	HB	CC	4H006

C07C29/03	.by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H₂O₂ [3]	HB	CC	4H006

C07C29/04	..by hydration of carbon-to-carbon double bonds	HB	CC	4H006

C07C29/05	...with formation of absorption products in mineral acids and their hydrolysis [3]	HB	CC	4H006

C07C29/06	....the acid being sulfuric acid [3]	HB	CC	4H006

C07C29/08	....the acid being phosphoric acid [3]	HB	CC	4H006

C07C29/09	.by hydrolysis (of esters of organic acids C07C 27/02) [3]	HB	CC	4H006

C07C29/10	..of ethers, including cyclic ethers, e.g. oxiranes	HB	CC	4H006

C07C29/12	..of esters of mineral acids [3]	HB	CC	4H006

C07C29/124	...of halides [3]	HB	CC	4H006

C07C29/128	.by alcoholysis (of esters of organic acids C07C 27/02) [3]	HB	CC	4H006

C07C29/132	.by reduction of an oxygen-containing functional group [3]	HB	CC	4H006

C07C29/136	..of	HB	CC	4H006

C07C29/14	...of a —CHO group [3]	HB	CC	4H006

C07C29/141	....with hydrogen or hydrogen-containing gases [5]	HB	CC	4H006

C07C29/143	...of ketones [5]	HB	CC	4H006

C07C29/145	....with hydrogen or hydrogen-containing gases [5]	HB	CC	4H006

C07C29/147	...of carboxylic acids or derivatives thereof [5]	HB	CC	4H006

C07C29/149	....with hydrogen or hydrogen-containing gases [5]	HB	CC	4H006

C07C29/15	.by reduction of oxides of carbon exclusively [3]	HB	CC	4H006

C07C29/151	..with hydrogen or hydrogen-containing gases [5]	HB	CC	4H006

C07C29/152	...characterised by the reactor used [5]	HB	CC	4H006

C07C29/153	...characterised by the catalyst used [5]	HB	CC	4H006

C07C29/154	....containing copper, silver, gold, or compounds thereof [5]	HB	CC	4H006

C07C29/156	....containing iron group metals, platinum group metals, or compounds thereof [5]	HB	CC	4H006

C07C29/157	.....containing platinum group metals or compounds thereof [5]	HB	CC	4H006

C07C29/158	......containing rhodium or compounds thereof [5]	HB	CC	4H006

C07C29/159	..with reducing agents other than hydrogen or hydrogen-containing gases [5]	HB	CC	4H006

C07C29/16	.by oxo-reaction combined with reduction	HB	CC	4H006

C07C29/17	.by hydrogenation of carbon-to-carbon double or triple bonds [3]	HB	CC	4H006

C07C29/19	..in six-membered aromatic rings [3]	HB	CC	4H006

C07C29/20	...in non-condensed rings substituted with hydroxy groups [3]	HB	CC	4H006

C07C29/32	.increasing the number of carbon atoms by reactions without formation of hydroxy groups [3]	HB	CC	4H006

C07C29/34	..by condensation involving hydroxy groups or the mineral ester groups derived therefrom, e.g. Guerbet reaction [3]	HB	CC	4H006

C07C29/36	.increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy groups, e.g. O-metal [3]	HB	CC	4H006

C07C29/38	..by reaction with aldehydes or ketones [3]	HB	CC	4H006

C07C29/40	...with compounds containing carbon-to-metal bonds [3]	HB	CC	4H006

C07C29/42	...with compounds containing triple carbon-to-carbon bonds, e.g. with metal-alkynes [3]	HB	CC	4H006

C07C29/44	.increasing the number of carbon atoms by addition reactions, i.e. reactions involving at least one carbon-to-carbon double or triple bond (C07C 29/16 takes precedence) [3]	HB	CC	4H006

C07C29/46	..by diene-synthesis [3]	HB	CC	4H006

C07C29/48	.by oxidation reactions with formation of hydroxy groups [3]	HB	CC	4H006

C07C29/50	..with molecular oxygen only [3]	HB	CC	4H006

C07C29/52	...in the presence of mineral boron compounds with, when necessary, hydrolysis of the intermediate formed [3]	HB	CC	4H006

C07C29/54	...starting from compounds containing carbon-to-metal bonds and followed by conversion of the O-metal to hydroxy groups [3]	HB	CC	4H006

C07C29/56	.by isomerisation [3]	HB	CC	4H006

C07C29/56@A	Oxirane ring R unsaturated alcohol	HB	CC	4H006

C07C29/56@B	Relocation of double bonds	HB	CC	4H006

C07C29/56@C	Cis-trans	HB	CC	4H006

C07C29/56@Z	Others	HB	CC	4H006

C07C29/58	.by elimination of halogen, e.g. by hydrogenolysis, splitting-off (C07C 29/124 takes precedence) [3]	HB	CC	4H006

C07C29/60	.by elimination of hydroxy groups, e.g. by dehydration (C07C 29/34 takes precedence) [3]	HB	CC	4H006

C07C29/62	.by introduction of halogen; by substitution of halogen atoms by other halogen atoms [3]	HB	CC	4H006

C07C29/64	.by simultaneous introduction of hydroxy groups and halogens [3]	HB	CC	4H006

C07C29/66	..by addition of hypohalogenous acids, which may be formed in situ, to carbon-to-carbon unsaturated bonds [3]	HB	CC	4H006

C07C29/68	.Preparation of metal-alcoholates (C07C 29/42, C07C 29/54 take precedence) [3]	HB	CC	4H006

C07C29/70	..by converting hydroxy groups to O-metal groups [3]	HB	CC	4H006

C07C29/72	..by oxidation of carbon-to-metal bonds [3]	HB	CC	4H006

C07C29/74	.Separation; Purification; Stabilisation; Use of additives [3]	HB	CC	4H006

C07C29/76	..by physical treatment [3]	HB	CC	4H006

C07C29/78	...by condensation or crystallisation [3]	HB	CC	4H006

C07C29/80	...by distillation [3]	HB	CC	4H006

C07C29/82	....by azeotropic distillation [3]	HB	CC	4H006

C07C29/84	....by extractive distillation [3]	HB	CC	4H006

C07C29/86	...by liquid-liquid treatment [3]	HB	CC	4H006

C07C29/88	..by treatment giving rise to a chemical modification of at least one compound (chemisorption C07C 29/76) [3]	HB	CC	4H006

C07C29/90	...using hydrogen only [3]	HB	CC	4H006

C07C29/92	...by a consecutive conversion and reconstruction [3]	HB	CC	4H006

C07C29/94	..Use of additives, e.g. for stabilisation [3]	HB	CC	4H006

This page displays all 「FI」 in main group C07C29/00.	HB:Handbook
	CC:Concordance