MASS SPECTROMETRY IN STRUCTURAL AND STEREOCHEMICAL PROBLEMS .41. ELECTRON IMPACT INDUCED ELIMINATION OF WATER FROM 3-HYDROXY STEROIDS

被引:61
作者
KARLINER, J
BUDZIKIE.H
DJERASSI, C
机构
关键词
D O I
10.1021/jo01341a015
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:710 / &
相关论文
共 20 条
[1]   MASS SPECTROMETRY IN STRUCTURAL + STEREOCHEMICAL PROBLEMS .35. MASS SPECTROMETRIC FRAGMENTATION + HYDROGEN TRANSFER REACTIONS IN 16-KETO STEROIDS . NOVEL SYNTHESIS OF SIDE CHAIN LABELED CHOLESTANES [J].
BEARD, C ;
DJERASSI, C ;
BUDZIKIEWICZ, H ;
WILSON, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (02) :269-&
[2]   RESEARCHES ON ACETYLENIC COMPOUNDS .1. THE PREPARATION OF ACETYLENIC KETONES BY OXIDATION OF ACETYLENIC CARBINOLS AND GLYCOLS [J].
BOWDEN, K ;
HEILBRON, IM ;
JONES, ERH ;
WEEDON, BCL .
JOURNAL OF THE CHEMICAL SOCIETY, 1946, (JAN) :39-45
[3]   LITHIUM TRI-TERT-BUTOXYALUMINOHYDRIDE - A NEW REAGENT FOR CONVERTING ACID CHLORIDES TO ALDEHYDES [J].
BROWN, HC ;
MCFARLIN, RF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (01) :252-252
[4]   MASSENSPEKTROMETRIE UND IHRE ANWENDUNG AUF STRUKTURELLE UND STEREOCHEMISCHE PROBLEME .67. ZUM RETRO-DIELS-ALDER-ZERFALL ORGANISCHER MOLEKULE UNTER ELEKTRONENBESCHUSS [J].
BUDZIKIEWICZ, H ;
BRAUMAN, JI ;
DJERASSI, C .
TETRAHEDRON, 1965, 21 (07) :1855-+
[5]  
BUDZIKIEWICZ H, 1964, MONATSH CHEM, V95, P158
[6]  
FIELD FH, 1957, ELECTRON IMPACT PHEN, pCH5
[7]   *UBER STEROIDE UND SEXUALHORMONE .160. 2-ALPHA, 3-ALPHA- UND 2-BETA, 3-BETA-OXIDO-CHLOLESTANE - KONFIGURATION DER 2-OXY-CHOLESTANE [J].
FURST, A ;
PLATTNER, PA .
HELVETICA CHIMICA ACTA, 1949, 32 (01) :275-283
[8]   MASS SPECTROMETRY IN STRUCTURAL + STEREOCHEMICAL PROBLEMS .59. MECHANISM OF FORMAL LOSS OF ACETONE FROM 2-OXO-5ALPHA-STEROIDS [J].
GURST, JE ;
DJERASSI, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (24) :5542-&
[9]   *UBER STEROIDE .110. HERSTELLUNG VON 7 9,11-DIENEN DER ANDROSTAN-REIHE [J].
HEUSLER, K ;
WETTSTEIN, A .
HELVETICA CHIMICA ACTA, 1952, 35 (01) :284-294
[10]  
HUANGMINLON, 1946, J AM CHEM SOC, V68, P2487, DOI DOI 10.1021/JA01216A013