STUDIES ON THE SYNTHESIS OF APHIDICOLIN - THE DIELS-ALDER ROUTE TO SPIROCYCLIC INTERMEDIATES

被引：11

作者：

BELL, VL ^{[1
]}

HOLMES, AB ^{[1
]}

HSU, SY ^{[1
]}

MOCK, GA ^{[1
]}

RAPHAEL, RA ^{[1
]}

机构：

[1] UNIV CAMBRIDGE,CHEM LAB,LENSFIELD RD,CAMBRIDGE CB2 1EW,ENGLAND

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1986年 / 08期

关键词：

D O I：

10.1039/p19860001507

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1507 / 1514

页数：8

共 57 条

[1] A H-2 NMR-STUDY OF THE REARRANGEMENT STEP IN APHIDICOLIN BIOSYNTHESIS
ACKLAND, MJ
HANSON, JR
RATCLIFFE, AH
SADLER, IH
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (03) : 165 - 166
[2] BIOSYNTHESIS OF DITERPENE ANTIBIOTIC, APHIDICOLIN, BY RADIOISOTOPE AND C-13 NUCLEAR MAGNETIC-RESONANCE METHODS
ADAMS, MR
BULOCK, JD
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1975, (10) : 389 - 391
[3] BABLER JH, 1983, SYNTH COMMUN, V14, P39
[4] AN IMPROVED SYNTHESIS OF 1,4-DITHIASPIRO[4.5] DECAN-8-ONE (CYCLOHEXANE-1,4-DIONE MONOTHIOACETAL)
BELL, VL
HOLMES, AB
[J]. SYNTHETIC COMMUNICATIONS, 1982, 12 (04) : 323 - 326
[5] A TOTAL SYNTHESIS OF APHIDICOLIN - STEREOSPECIFIC SYNTHESIS OF (+0-)-3-ALPHA,18-DIHYDROXY-17-NORAPHIDICOLAN-16-ONE
BETTOLO, RM
TAGLIATESTA, P
LUPI, A
BRAVETTI, D
[J]. HELVETICA CHIMICA ACTA, 1983, 66 (07) : 1922 - 1928
[6] A STEREOSELECTIVE TOTAL SYNTHESIS OF (+/-)-MARITIMOL, (+/-)-2-DEOXYSTEMODINONE, (+/-)-STEMODINONE, AND (+/-)-STEMODIN
BETTOLO, RM
TAGLIATESTA, P
LUPI, A
BRAVETTI, D
[J]. HELVETICA CHIMICA ACTA, 1983, 66 (03) : 760 - 770
[7] BROOME MG, 1981, 72ND P ANN M AM ASS, V22, P202
[8] METHYLENEKETENES AND METHYLENECARBENES .6. PYROLYTIC GENERATION OF ACYLOXYCARBENES AND THEIR REARRANGEMENT TO 1,2-DIKETONES
BROWN, RFC
EASTWOOD, FW
LIM, ST
MCMULLEN, GL
[J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1976, 29 (08) : 1705 - 1712
[9] SYNTHESIS OF APHIDICOLIN - PRELIMINARY STUDIES
CARGILL, RL
BUSHEY, DF
DALTON, JR
PRASAD, RS
DYER, RD
BORDNER, J
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (17) : 3389 - 3399
[10] CAZEAU P, 1972, B SOC CHIM FR, P1658

← 1 2 3 4 5 6 →