24СʱÈÈÃŰæ¿éÅÅÐаñ    

Znn3bq.jpeg
ÉÇÍ·´óѧº£Ñó¿ÆÑ§½ÓÊܵ÷¼Á
²é¿´: 993  |  »Ø¸´: 6
µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû

ÏÄСÃÀ123456

гæ (³õÈëÎÄ̳)

[ÇóÖú] ÇóÖú2¸ö΢Æ×Êý¾Ý

1£º
¦Ä C (151 MHz, DMSO) 183.2, 154.90, 101.92, 68.06, 50.61, 47.87, 44.72, 43.57, 42.49,  39.15, 38.41, 37.76, 37.52, 37.48, 35.11, 31.46, 27.82, 22.06, 20.74, 18.81.
2£º
¦Ä C (151 MHz, CDCl3) 155.31, 102.22, 81.20, 64.65, 51.45, 48.93, 43.52, 43.16, 39.64, 39.08, 38.35, 37.88, 37.00, 33.92, 32.46, 28.26, 28.11, 23.54, 22.37, 20.39.
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

audreygc

Ìú¸Ëľ³æ (ÕýʽдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ͬѧ£¬Äã´ÓСµ½´óÔÙ·¢Ò»´Î°É¡£Òª²»È»²é×ÅÌ«Âé·³¡£
3Â¥2012-11-21 10:28:50
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
²é¿´È«²¿ 7 ¸ö»Ø´ð

ľ·ç·ãpan

ľ³æ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
11 .     19-(N,N-dimethylcarbamoxy)-2¦Â,13-dihydroxystemarane
C23H39NO4     ÏàËÆ¶È:63.6%
Phytochemistry          2006          67          1088-1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamm, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     2¦Á,3¦Â-dihydroxypregnan-16-one 2¦Â,19-hemiketal
C21H32O4     ÏàËÆ¶È:61.9%
Phytochemistry          1997          45          1495-1500
Androstane and pregnane 2¦Â, 19-hemiketal steroids from Trichilia claussenii
Mônica T. Pupo, Paulo C. Vieira, João B. Fernandes, M. F¨¢tima das G.F. da Silva, Edson Rodrigues Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     ent-kaur-16-ene-9-ol
    ÏàËÆ¶È:61.9%
Phytochemistry          1992          31          1553-1559
Minor diterpene glycosides from sweet leaves of Rubus suavissimus
Kazuhiro Ohtani, Yoko Aikawa, Ryoji Kasai, Wen-Hua Chou, Kazuo Yamasaki, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     Methyl-ent-pimar-9(11)en-19-oate
    ÏàËÆ¶È:61.9%
Phytochemistry          1986          25          1240-1242
Pimaradiene diterpenes from mikania triangularis
Fernanda S. Knudsen, Wagner Vilegas, Fernando Oliveira, Nidia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     3¦Â-Acetoxy-7¦Á-hydroxyandrost-5-en-17-one
    ÏàËÆ¶È:61.9%
Steroids          1996          61          453-460
Steroidal allylic fluorination using diethylaminosulfur trifluoride: A convenient method for the synthesis of 3¦Â-acetoxy-7¦Á-and 7¦Â-fluoroandrost-5-en-17-one
Padma Marwah, James B. Thoden, Douglas R. Powell, Henry A. Lardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     isodehydropopulifolic acid methyl ester
    ÏàËÆ¶È:61.9%
Tetrahedron          1994          50          10791-10802
Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius
Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jim¨¦nez, Anna M. Lithgow, Margarita L¨®pez, Rosalina F. Moro, Antonio G¨®mez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ  
2:1 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2004          65          701-710
Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2004          65          2211-2217
Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     alcohol
C18H32O     ÏàËÆ¶È:65%
Journal of Natural Products          1997          60          1261-1264
Cyclic Peroxides and Related Norterpenes from a Southern Australian Marine Sponge, Mycale sp.
Robert J. Capon, Simone J. Rochfort, and Simon P. B. Ovenden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     compound 2
C20H32O2     ÏàËÆ¶È:65%
Phytochemistry          1980          19          1237-1238
Kaurenoid diterpenes from Stachys lanata
Franco Piozzi, Giuseppe Savona, James R. Hanson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     Ent-3¦Á-hydroxykaur-16-ene
    ÏàËÆ¶È:65%
Journal of the Brazilian Chemical Society          2004          15          767-772
Terpenoid Constituents from Leaves of Guarea kunthiana
Fernanda R. Garcez, Walmir S. Garcez, Ana Francisca G. da Silva, Rita de C¨¢ssia Bazzo and Ubirazilda M. Resende
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     methyl ent-isopimara-9(11),15-diene-oic acid
C21H32O2     ÏàËÆ¶È:61.9%
Phytochemistry          1991          30          3365-3368
Diterpenes from Calceolaria polifolia
Maria C. Chamy, Marisa Piovano, Juan A. Garbarino, Vicente Gambaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     Compound 9
    ÏàËÆ¶È:61.9%
Phytochemical Analysis          1993          4          19-24
Carbon-13 nuclear magnetic resonance spectra of some tetracyclic diterpenoids isolated from Elaeoselinum species
Manuel Grande, Joaqu¨ªn R. Mor¨¢n, Mar¨ªa Jes¨²s Mac¨ªas and Balbino Mancheño
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-11-21 10:28:29
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ľ·ç·ãpan

ľ³æ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

µÚÒ»¸ö»¯ºÏÎ1 .     19-(N,N-dimethylcarbamoxy)-2¦Â,13-dihydroxystemarane
C23H39NO4     ÏàËÆ¶È:63.6%
Phytochemistry          2006          67          1088-1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamm, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     2¦Á,3¦Â-dihydroxypregnan-16-one 2¦Â,19-hemiketal
C21H32O4     ÏàËÆ¶È:61.9%
Phytochemistry          1997          45          1495-1500
Androstane and pregnane 2¦Â, 19-hemiketal steroids from Trichilia claussenii
Mônica T. Pupo, Paulo C. Vieira, João B. Fernandes, M. F¨¢tima das G.F. da Silva, Edson Rodrigues Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     ent-kaur-16-ene-9-ol
    ÏàËÆ¶È:61.9%
Phytochemistry          1992          31          1553-1559
Minor diterpene glycosides from sweet leaves of Rubus suavissimus
Kazuhiro Ohtani, Yoko Aikawa, Ryoji Kasai, Wen-Hua Chou, Kazuo Yamasaki, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     Methyl-ent-pimar-9(11)en-19-oate
    ÏàËÆ¶È:61.9%
Phytochemistry          1986          25          1240-1242
Pimaradiene diterpenes from mikania triangularis
Fernanda S. Knudsen, Wagner Vilegas, Fernando Oliveira, Nidia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     3¦Â-Acetoxy-7¦Á-hydroxyandrost-5-en-17-one
    ÏàËÆ¶È:61.9%
Steroids          1996          61          453-460
Steroidal allylic fluorination using diethylaminosulfur trifluoride: A convenient method for the synthesis of 3¦Â-acetoxy-7¦Á-and 7¦Â-fluoroandrost-5-en-17-one
Padma Marwah, James B. Thoden, Douglas R. Powell, Henry A. Lardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     isodehydropopulifolic acid methyl ester
    ÏàËÆ¶È:61.9%
Tetrahedron          1994          50          10791-10802
Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius
Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jim¨¦nez, Anna M. Lithgow, Margarita L¨®pez, Rosalina F. Moro, Antonio G¨®mez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ  
µÚ¶þ¸ö»¯ºÏÎï
1 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2004          65          701-710
Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2004          65          2211-2217
Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Glenroy D.A. Martin, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     stemodin
    ÏàËÆ¶È:65%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     alcohol
C18H32O     ÏàËÆ¶È:65%
Journal of Natural Products          1997          60          1261-1264
Cyclic Peroxides and Related Norterpenes from a Southern Australian Marine Sponge, Mycale sp.
Robert J. Capon, Simone J. Rochfort, and Simon P. B. Ovenden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     compound 2
C20H32O2     ÏàËÆ¶È:65%
Phytochemistry          1980          19          1237-1238
Kaurenoid diterpenes from Stachys lanata
Franco Piozzi, Giuseppe Savona, James R. Hanson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     Ent-3¦Á-hydroxykaur-16-ene
    ÏàËÆ¶È:65%
Journal of the Brazilian Chemical Society          2004          15          767-772
Terpenoid Constituents from Leaves of Guarea kunthiana
Fernanda R. Garcez, Walmir S. Garcez, Ana Francisca G. da Silva, Rita de C¨¢ssia Bazzo and Ubirazilda M. Resende
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     methyl ent-isopimara-9(11),15-diene-oic acid
C21H32O2     ÏàËÆ¶È:61.9%
Phytochemistry          1991          30          3365-3368
Diterpenes from Calceolaria polifolia
Maria C. Chamy, Marisa Piovano, Juan A. Garbarino, Vicente Gambaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     Compound 9
    ÏàËÆ¶È:61.9%
Phytochemical Analysis          1993          4          19-24
Carbon-13 nuclear magnetic resonance spectra of some tetracyclic diterpenoids isolated from Elaeoselinum species
Manuel Grande, Joaqu¨ªn R. Mor¨¢n, Mar¨ªa Jes¨²s Mac¨ªas and Balbino Mancheño
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2012-11-21 10:33:33
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ľ·ç·ãpan

ľ³æ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
ÏÄСÃÀ123456: ½ð±Ò+15 2012-11-21 11:08:23
ÒýÓûØÌû:
3Â¥: Originally posted by audreygc at 2012-11-21 10:28:50
ͬѧ£¬Äã´ÓСµ½´óÔÙ·¢Ò»´Î°É¡£Òª²»È»²é×ÅÌ«Âé·³¡£

ÎÒ¶¼Êǰ´ÏàËÆ¶ÈÓÉ´óµ½Ð¡¸øÄã·¢µÄ ÄãµÃÂýÂý¶ÔÆ×
5Â¥2012-11-21 10:34:33
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] »¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô +26 yzyzx 2026-04-12 29/1450 2026-04-14 01:48 by BruceLiu320
[¿¼ÑÐ] 284Çóµ÷¼Á +16 ÈÃÎÒÉϰ¶°É°¢Î÷ 2026-04-09 16/800 2026-04-13 22:18 by pies112
[¿¼ÑÐ] 291 Çóµ÷¼Á +33 »¯¹¤2026½ì±ÏÒµÉ 2026-04-09 33/1650 2026-04-13 22:16 by pies112
[¿¼ÑÐ] ²ÄÁϸ´ÊÔÇóµ÷¼Á +24 xhhdjdjsjks 2026-04-09 24/1200 2026-04-13 15:49 by ÐÒÃâ ..
[¿¼ÑÐ] һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á +8 Ľ¾øcc 2026-04-09 8/400 2026-04-13 14:08 by ÕÅzhihao
[¿¼ÑÐ] Çóµ÷¼Á +16 ÕÅ·¬ÇѲ»³´µ° 2026-04-10 17/850 2026-04-12 13:58 by °¾Ò¹³É£¡
[¿¼ÑÐ] 305Çóµ÷¼Á +6 77Qi 2026-04-07 6/300 2026-04-12 02:30 by Çï¶¹²ËÑ¿
[¿¼ÑÐ] 359Çóµ÷¼Á +5 θ¾·ÂÎÀÛÁË 2026-04-11 5/250 2026-04-11 19:55 by lbsjt
[¿¼ÑÐ] 269Çóµ÷¼Á +11 °¡°¡ÎÒÎÒ 2026-04-07 11/550 2026-04-11 16:45 by vgtyfty
[¿¼ÑÐ] 0859£¬337Çóµ÷¼Á +4 ÑÐs. 2026-04-10 4/200 2026-04-11 11:34 by caotw2020
[¿¼ÑÐ] ÖÐҩѧµ÷¼Á ³õÊÔ324 +4 Ñó¸Ê¾Õ¡¢ 2026-04-10 6/300 2026-04-11 09:41 by gong120082
[¿¼ÑÐ] 296Çóµ÷¼Á +6 Íô£¡£¿£¡ 2026-04-08 6/300 2026-04-10 11:02 by mattzhming
[¿¼ÑÐ] Ò»Ö¾Ô¸ÖÐÄÏ´óѧÎïÀíѧ£¬Ó¢Ò»66£¬Çóµ÷¼Á +4 ³¤ÑÌì½ì» 2026-04-08 5/250 2026-04-10 10:31 by Ó±¹û¶ù
[¿¼ÑÐ] Ò»Ö¾Ô¸Öпƴó070300»¯Ñ§£¬314·ÖÇóµ÷¼Á +12 wakeluofu 2026-04-09 12/600 2026-04-10 09:57 by liuhuiying09
[¿¼ÑÐ] 348Çóµ÷¼Á +3 candyyyi 2026-04-09 3/150 2026-04-09 17:20 by ¶ÎΰÑÞ
[¿¼ÑÐ] Çóµ÷¼Á²ÄÁÏ¿ÆÑ§Ó빤³ÌÒ»Ö¾Ô¸985³õÊÔ365·Ö +5 ²Ä»¯Àî¿É 2026-04-08 5/250 2026-04-09 17:00 by Lilly_Li
[¿¼ÑÐ] 265Çóµ÷¼Á +4 ·ç˵ËýÔçÍüÁË 2026-04-07 4/200 2026-04-09 13:59 by onlyÖÜ
[¿¼ÑÐ] 293·ÖÇóµ÷¼Á£¬ÍâÓïΪ¶íÓï +7 ¼ÓÒ»Ò»¾Å 2026-04-07 10/500 2026-04-08 20:14 by yutian743
[¿¼ÑÐ] Çó¿¼ÑвÄÁϵ÷¼Á +3 ²Ä»¯Àî¿É 2026-04-07 3/150 2026-04-08 00:21 by JourneyLucky
[¿¼ÑÐ] 313Çóµ÷¼Á +3 Ê®Áùʰ½ 2026-04-07 3/150 2026-04-07 23:20 by lbsjt
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û