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이우영,조숙,고승권,이병익,황성욱,박지현,김우성,원영석 대한산부인과학회 1998 Obstetrics & Gynecology Science Vol.41 No.2
Hormonal replacement therapy(HRT) prevents postmenopausal bone loss by inhibiting bone resorption. Several case-control studies have shown that HRT appeared to be more effective for older women than early menopausal women, and women who had low bone mineral density(BMD) were better responded than women had high BMD on HRT. A retrospective study was performed to clarify whether the later postmenopausal use of HRT was more effective. BMD was measured prior to HRT and 1 year after the treatment in 83 menopausal women. The result was compared with 10 women who didn`t take HRT. Spinal BMD was increased in HRT users by 4.23%(p=0.0001), but decreased in nonusers by 2.1%(p= 0.232). The difference according to HRT regimen didn`t show any statistical significance. The longer the duration of menopause and the lower the initial bone mineral density, the highr the effectiveness of HRT was noted. Two(33.3%) of 6 women who had taken HRT within 3 years after menopause lowered the fracture risk, but only one(5.2%) in 19 women who had taken HRT after 3 years from menopause improved the bone mineral density above the fracture threshold. This study revealed that the earlier HRT might be more effective to keep the spinal BMD above the fracture threshold and to prevent osteoprosis in menopausal women.
이우영,Lee Woo Young Korean Chemical Society 1978 대한화학회지 Vol.22 No.5
Tetrazonium 염을 거쳐서 m-phenylenedihydrazine (MPDH)을 합성할 수 있었다. 즉, m-phenylenediamine을 진한 염산의 매질 속에서 $-10∼-5^{\circ}C$로 유지하고아질산나트륨으로 테트라 아조화한 다음, 이때 생긴 tetrazonium 염을 염화주석(II)으로 환원시켜 MPDH를 염산염의 꼴로 얻어 알코올에서 재결정 할 수 있었다. MPDH의 유리염기는 불안정하기 때문에 공기 중에서는 안정한 상태로 얻기 어려우며, 그 염산염은 명확한 녹는 점을 가지지 않고 $185^{\circ}C$에서 분해하였다. MPDH도 방향족 monohydrazine의 경우 처럼 mono 또는 dicarbnyl 화합물과 쉽게 축합반응을 일으켜서 dihydrazone 또는 고리모양 화합물을 생성하였다. MPDH와 carbonyl 화합물과의 반응에서 얻은 여러가지 화합물의 구조를 결정하였다. m-Phenylenedihydrazine(MPDH) was prepared via tetrazonium salt: m-Phenylenediamine was tetrazotized with sodium nitrite at $-10∼-5^{\circ}C$ in concentrated hydrochloric acid medium, reused tetrazonium salt was reduced with stannous chloride and MPDH was separated as dihydrochloride which was recrystallized from alcohol. The free base of MPDH being unstable it could hardly be obtained in the air. $MPDH{\cdot}2HCl$ did not show sharp melting point but decomposed at $185^{\circ}C$. MPDH, like aromatic monohydrazines, condensed with mono-and dicarbonyl compounds giving dihydrazones or cyclic compounds. The structures of condensation products obtained from the reaction of MPDH with carbonyl compounds are determined.
이우영,Lee Woo Young Korean Chemical Society 1976 대한화학회지 Vol.20 No.6
파라페닐렌디히드라진(PPDH)과 디카르보닐化合物을 반응시켜서 생기는 縮合生成物들의 構造를 밝혔다. 아세틸아세톤과의 반응에서는 고리화합물인 1,1'-p-페닐린-bis-3-메틸-5-피라졸론이 얻어졌으며, 디아세틸과의 반응에서는 역시 고리화합물인 1,1'-p-페닐렌-bis-메틸-5-피라졸론이 얻어졌으며, 디아세틸과의 반응에서는 디아세틸 p-페닐렌디히라존이 生成되었다. 그 밖의 디카르보닐화합물에서 얻은 축합생성물은 불안정하여 구조결정이 어려웠다. Structures of the products obtained from the condensation reaction between p-phenylenedihydrazine(PPDH) and dicarbonyl compounds were determined, From the reaction with PPDH, acetylacetone produced a cyclic compound, 1,1'-p-phenylene-bis-3, 5-dimetylpyrazole; ethylacetoacetate also formed a cyclic compound, 1,1'-p-phenylene-bis-3-methyl-5-pyrazolone; diacetyl yielded a simple dihydrazone, diacetyl p-phenylenedihydrazone. Condensation products from the other dicarbonyl compounds being of generally unstable, the structure determination was quite difficult.
방향족 디아민의 Tetrazo 화에 관한 연구 (제1보). 염산 및과염소산 중에서 p-Phenylenediamine의 Tetrazo 화
이우영,이윤영,장세희,Woo Young Lee,Youn Young Lee,Sae Hee Chang 대한화학회 1973 대한화학회지 Vol.17 No.4
p-Phenylenediamine을 과량의 진한 염산 및 과염소산을 매질로하여 거의 완전히 tetrazo화 하였다. Tetrazonium염의 두 diazo기를 할로겐으로 치환하여 생긴 dihalobenzene의 수량으로 반응의 정도를 알아 보았다. 이 반응의 성패는 tetrazonium염의 안정도에 의하여 죄우되었으며, 그 안정도는 매질의 종류, 산도(농도) 및 그양과 밀접한 관계가 있음을 알았다. 즉 산매질의 농도가 너무 묽으면 tetrazonium염은 불안정하여 완전히 분해되었으며, 매질의 농도가 너무 진하면 tetrazonium염은 안정한 반면에 tetrazo화 반응이 방해되었다. 이 상반되는 두 경향을 조화시키기 위해서는 tetrazonium염이 안정하게 존재할 수 있는 가장 낮은 농도의 산을 매질로 써야함을 알 수 있었다. p-Phenylenediamine의 tetrazo화에서는 약$40{\sim}45$%의 산매질이 적당하였다. $H^+$이온이 부촉매로 작용하는 것으로 보아 diazo화 반응이 아민의 염의 상태에서 일어나는 것이아니고 유리상태의 아민과 nitroso group 사이에서 일어난다는 설이 타당함을 알 수 있었다. Tetrazo화 반응을 diazo화 반응의 kinetics 및 mechanism과 관련시켜서 설명하였다. p-Phenylenediamine was tetrazotized with sodium nitrite in an excess amount of concentrated hydrochloric acid media at -10$^{\circ}$C. It was also tetrazotized almost completely in 45% perchloric acid media. The two diazo groups in the tetrazonium salt were substituted by halogen, and the degree of tetrazotization reaction was observed by dihalobenzene yielded. The result of the tetrazotization was dependent upon the stability of the tetrazonium salt, and the stability was determined by concentration and quantity of the acid media. In dilute acid media the tetrazonium salt was unstable and completely decomposed. In concentrated acid media, though the tetrazonium salt was stable, tetrazotization reaction was retarded. To harmonize the two opposing tendencies it was advisable to find the optimum acidity of media at which the salt was fairly stable. About $40{\sim}45$% of the acid media was suitable. The fact that the $H^+$ ion behaved as a negative catalyst supported the assumption that the diazotization reaction is primarily a reaction between the free amine and a nitroso group. The reaction of tetrazotization is expressed with respect to the kinetics and mechanism of diazotization.