Volatile:ShowField

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ID Value
LBF15306CV01 Optical=[ α ]D -17.1°(C 0.48, CHCl3) [[Reference:Iwashima_M:Okamoto_K:Iguchi_K:,Tetrahedron Lett.,1999,40,6455
LBF15306CV02 Optical=[ α ]D -33.7°(C 0.43, CHCl3)[[Reference:Iwashima_M:Okamoto_K:Iguchi_K:,Tetrahedron Lett.,1999,40,6455
LBF17307HO02 Optical=METHYL ESTER ; [ α ]25
D
   =+7.5°(C=0.2, CHLOROFORM) [[Reference:Nicolaou_KC:Stylianides_NA:Ramphal_JY:,J. Chem. Soc. Perkin Trans. I,1989,,2131
LBF18107PG01 Optical=[ α ]20.2
D
   = +16.9° (C=1.76 CHLOROFORM, measured after 24 hours at 20°C)
LBF20107PG01 Optical=[ α ]578=-61.6°(C=0.56, TETRAHYDROFURAN) [[Reference:Corey_EJ:Vlattas_I:Harding_K:,J. Am. Chem. Soc.,1969,91,535
LBF20107PG02 Optical=[ α ]X20
D
   =-50°(C=1.55, METHANOL) [[Reference:Tanaka_T:Hazato_A:Bannai_K:Okamura_N:Sugiura_S:Manabe_K:Toru_T:Kurozumi_S:Suzuki_M:Kawagishi_T_et_al:,Tetrahedron,1987,43,813
LBF20107PG03 Optical=[ α ]X25
D
   =+30°(ETHANOL) [[Reference:Pike_JE:Lincoln_FH:Schneider_WP:,J. Org. Chem.,1969,34,3552
LBF20107PG18 Optical=[ α ]21
D
   = -9.6° (C=1.04 METHANOL) [[Reference:Tanaka_T:Hazato_A:Bannai_K:Okamura_N:Sugiura_S:Manabe_K:Toru_T:Kurozumi_S:Suzuki_M:Kawagishi_T_et_al:,Tetrahedron,1987,43,813
LBF20207PG01 Optical=ORD (H2O, C=0.0040g/ml) : 256(+35.000°), 220(-43.000°) [[Reference:Andersen_NH:,J. Lipid Res.,1969,10,320
LBF20207PG22 Optical=[ α ]20
D
   =9° (C=2.11,THF) [[Reference:Ogawa_Y:Nunomoto_M:Shibasaki_M:,J. Org. Chem.,1986,51,1625
LBF20207PG23 Optical=[ α ]26
D
   =-61.0°(C=1.0, TETRAHYDROFURAN) [[Reference:Corey_EJ:Schaaf_TK:Huber_W:Koelliker_U:Weinshenker_NM:,J. Am. Chem. Soc.,1970,92,397
LBF20207PG25 Optical=[ α ]25
D
   =23.8 °(C=1,THF) [[Reference:Corey_EJ:Schaaf_TK:Huber_W:Koelliker_U:Weinshenker_NM:,J. Am. Chem. Soc.,1970,92,397
LBF20207PG51 Optical=[ α ]D=78°(C=0.8820, CHCl3) [[Reference:Johnson_RA:Lincoln_FH:Nidy_EG:Schneider_WP:Thompson_JL:Axen_U:,J. Am. Chem. Soc.,1978,100,7690
LBF20207TX02 Optical=[ α ]25
D
   =57.4°(C=0.26 ETHYL ACETATE) [[Reference:Hanessian_S:Lavallee_P:,Can. J. Chem.,1977,55,562
LBF20303PG03 Optical=[ α ]24
D
   =-48.9°(C=1.2, TETRAHYDROFURAN) [[Reference:Corey_EJ:Shirahama_H:Yamamoto_H:Terashima_S:Venkateswarlu_A:Schaaf_TK:,J. Am. Chem. Soc.,1971,93,1490
LBF20303PG04 Optical=[ α ]26
D
   =+29.6°(C=0.54, TETRAHYDROFURAN) [[Reference:Corey_EJ:Shirahama_H:Yamamoto_H:Terashima_S:Venkateswarlu_A:Schaaf_TK:,J. Am. Chem. Soc.,1971,93,1490
LBF20306CV01 Optical=[ α ]D -168.0°[[Reference:Iwashima_M:Watanabe_K:Iguchi_K:,Tetrahedron Lett.,1997,38,8319
LBF20306CV02 Optical=[ α ]D -110°[[Reference:Iwashima_M:Watanabe_K:Iguchi_K:,Tetrahedron Lett.,1997,38,8319
LBF20306CV03 Optical=[ α ]D -24.1°(C 0.44, CHCl3)[[Reference:Iguchi_K:Kaneta_S:Mori_K:Yamada_Y:Honda_A:Mori_Y:,Tetrahedron Lett.,1985,26,5787
LBF20306EO03 Optical=11(R),12(S)-EET METHYL ESTER ; [ α ]23
D
  =+4.94°(C=1.64, ACETONE) [[Reference:Mosset_P:Yadagiri_P:Lumin_S:Capdevila_J:Falck_JR:,Tetrahedron_Lett.,1986,27,6035
LBF20306HO07 Optical=METHYL ESTER ; [ α ]23
D
   =-3.0°(C=0.8, ACETONE) [[Reference:Shin_DS:Yadagiri_P:Falck_JR:Masferrer_JL:Schwartzman_ML:,Tetrah. Lett.,1989,30,3923
LBF20306HX04 Optical=ACETATE, METHYL ESTER ; [ α ]X23
D
   =-10.9°(C=0.11, CHLOROFORM) [[Reference:Moghaddam_MF:Gerwick_WH:Ballantine_DL:,J. Biol. Chem.,1990,265,6126
LBF20307PG01 Optical=[ α ]X20
D
   =+140°(C=1.15, CHLOROFORM) [[Reference:Corey_EJ:Moinet_G:,J. Am. Chem. Soc.,1973,95,6331
LBF20307PG41 Optical=[ α ]D +128°(CHCl3)[[Reference:Bundy_GL:Daniels_EG:Lincoln_FH:Pike_JE:,J. Am. Chem. Soc.,1972,94,2124
LBF20406AM02 Optical=[ α ]25
4
   = -8.9°(C=1,CHCl3)[[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659
LBF20406AM03 Optical=[ α ]25
4
   = +8.9° [[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659
LBF20406AM14 Optical=[ α ]25
4
   = -7.08°(c=l,EtOH)[[Reference:Sheskin_T:Hanus_L:Slager_J:Vogel_Z:Mechoulam_R:,J. Med. Chem.,1997,40,659
LBF20406AM15 Optical=[ α ]25
4
   = +7.08° (C=1, EtOH) [[Reference:Bergstrom_S:,Science,1967,157,382
LBF20406AM37 Optical=[ α ]25
4
   = +10.9° [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889
LBF20406AM38 Optical=[ α ]25
4
   = +9.44° [[Reference:Abadji_V:Lin_S:Taha_G:Griffin_G:Stevenson_LA:Pertwee_RG:Makriyannis_A:,J. Med. Chem.,1994,37,1889
LBF20406CV01 Optical=[ α ]D -25.6°(C 0.26, CHCl3)[[Reference:Iguchi_K:Iwashima_M:Watanabe_K:,J. Nat. Prod.,1995,58,790
LBF20406CV02 Optical=[ α ]D -7.3°(C 0.21, CHCl3)[[Reference:Iguchi_K:Iwashima_M:Watanabe_K:,J. Nat. Prod.,1995,58,790
LBF20406CV03 Optical=[ α ]D -18.7°(C 0.30, CHCl3)[[Reference:Iwashima_M:Okamoto_K:Miyai_Y:Iguchi_K:,Chem. Pharm. Bull. (Tokyo),1999,47,884
LBF20406CV04 Optical=[ α ]D -10.0°(C 0.06, CHCl3)[[Reference:Iwashima_M:Okamoto_K:Miyai_Y:Iguchi_K:,Chem. Pharm. Bull. (Tokyo),1999,47,884
LBF20406CV05 Optical=[ α ]D -28.9°(C 0.36, CHCl3)[[Reference:Kikuchi_H:Tsukitani_Y:Iguchi_K:Yamada_Y:,Tetrahedron Lett.,1982,23,5171
LBF20406CV06 Optical=[ α ]D +10.9°(C 0.35, CHCl3)[[Reference:Kikuchi_H:Tsukitani_Y:Iguchi_K:Yamada_Y:,Tetrahedron Lett.,1982,23,5171
LBF20406CV07 Optical=[ α ]D +45.5°(C 0.22, CHCl3)[[Reference:Kikuchi_H:Tsukitani_Y:Iguchi_K:Yamada_Y:,Tetrahedron Lett.,1982,23,5171
LBF20406CV08 Optical=[ α ]D -80.0°(CHCl3)[[Reference:Kikuchi_H:Tsukitani_Y:Iguchi_K:Yamada_Y:,Tennen Yuki Kagoubutsu Toronkai Koen Yoshishu 26th,1983,26,220
LBF20406CV09 Optical=[ α ]D -31.1°(C 0.09, CHCl3)[[Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433
LBF20406CV10 Optical=[ α ]D +3.7°(C 0.54, CHCl3)[[Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433
LBF20406CV11 Optical=[ α ]D +26.4°(C 0.86, CHCl3)[[Reference:Iguchi_K:Yamada_Y:Kikuchi_H:Tsukitani_Y:,Tetrahedron Lett.,1983,24,4433
LBF20406CV12 Optical=[ α ]D -1.2°(C 0.17, CHCl3)[[Reference:Iguchi_K:Kaneta_S:Mori_K:Yamada_Y:Honda_A:Mori_Y:,Tetrahedron Lett.,1985,26,5787
LBF20406CV13 Optical=[ α ]D +22.7°(C 0.075, CHCl3)[[Reference:Iguchi_K:Kaneta_S:Mori_K:Yamada_Y:Honda_A:Mori_Y:,Tetrahedron Lett.,1985,26,5787
LBF20406CV14 Optical=[ α ]D +27.3°(C 0.033, CHCl3)[[Reference:Iguchi_K:Kaneta_S:Mori_K:Yamada_Y:Honda_A:Mori_Y:,Tetrahedron Lett.,1985,26,5787
LBF20406CV15 Optical=12-O-acetylchlorovulone IV[ α ]D -12°(C 0.025, CHCl3)[[Reference:Iguchi_K:Kaneta_S:Mori_K:Yamada_Y:Honda_A:Mori_Y:,Tetrahedron Lett.,1985,26,5787
LBF20406CV16 Optical=[ α ]D +6.0°(C 0.05, MeOH)(Yamada Yasuji)
LBF20406CV17 Optical=[ α ]D +15.2°(C 0.07, MeOH)(Yamada Yasuji)
LBF20406CV18 Optical=[ α ]D -7.8°(C 0.26, CHCl3)[[Reference:Iwashima_M:Okamoto_K:Konno_F:Iguchi_K:,J. Nat. Prod.,1999,62,352
LBF20406HO20 Optical=METHYL ESTER ; [ α ]23
D
   =+14.0°(C=2.0, BENZENE)
LBF20406HO21 Optical=METHYL ESTER ; [ α ]25
D
   =+1.50°(C=0.2, CHLOROFORM) [[Reference:Corey_EJ:Niwa_H:Knolle_J:,J. Am. Chem. Soc.,1978,100,1942
LBF20406HO22 Optical=8(S)-ISOMER METHYL ESTER ; [ α ]22
D
   =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039
LBF20406LT01 Optical=[ α ]25
D
   =-21.9°(C=0.32,CYCLOHEXANE) [[Reference:Corey_EJ:Clark_DA:Goto_G:Marfat_A:Mioskowski_C:Samuelsson_B:Hammarstroem_S:,J. Am. Chem. Soc.,1980,102,1436
LBF20406LT17 Optical=DIMETHYL ESTER ; [ α ]20
D
   =+35.2° [[Reference:Rosenberger_M:Newkom_C:Aig_ER:,J. Am. Chem. Soc.,1983,105,3656


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