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         ¹úÍâһЩ¿ÆÑлù½ð»áºÍͳ¼Æ¾Öµ÷²éÖøÃû¿ÆÑ§¼Ò¶ÔÓÚ¿ÆÑй¤×÷µÄʱ¼ä·ÖÅä, ½á¹ûÈçÏÂ: ¼Æ»® 8 %, ÎÄÏײéÔÄ 51 %, ʵÑé 32 %, ±àд±¨¸æ 9 %. ÓÉÉÏÃæ×ÊÁÏ¿ÉÒÔÖªµÀÎÄÏ××ÊÁϲéÔĵÄÖØÒªÐÔ.
         ÎÄÏ×°´ÄÚÈÝÇø·ÖÓÐÒ»´ÎÎÄÏ×, ¶þ´ÎÎÄÏ׺ÍÈý´ÎÎÄÏ×. Ò»´ÎÎÄÏ×¼´Ô­Ê¼ÎÄÏ×, ÀýÈçÆÚ¿¯, ÔÓÖ¾, רÀûµÈ×÷ÕßÖ±½Ó±¨µ¼µÄ¿ÆÑÐÂÛÎÄ. ¶þ´ÎÎÄÏ×Ö¸¼ìË÷Ò»´ÎÎÄÏ׵Ť¾ßÊé, ÀýÈçÃÀ¹ú»¯Ñ§ÎÄÕª¼°ÆäÏà¹ØË÷Òý. Èý´ÎÎÄÏ×Ϊ½«Ô­Ê¼ÂÛÎÄÊý¾Ý¹éÄÉÕûÀíÐγɵÄ×ÛºÏ×ÊÁÏ, ÀýÈç×ÛÊö, ͼÊé, ´Êµä, °Ù¿ÆÈ«Êé, ÊÖ²áµÈ.
        ÏÂÃæ¼òÊö¼¸ÖÖ³£ÓõÄÓлú»¯Ñ§ÎÄÏ×:

                (Ò»). Èý´ÎÎÄÏ×
        (1). ´ÊµäÀà:
        i). Ó¢ºº,ººÓ¢»¯Ñ§»¯¹¤´ó´Êµä: ±à¼­¼ò½àÃ÷ÁË, ÊDzéÔÄ»¯Ñ§Ãû´ÊÓ¢·­ÖлòÖз­Ó¢·½±ãʡʱµÄ¹¤¾ßÊé. ÔĶÁÓ¢ÎÄ»¯Ñ§Êé¼®»òÆÚ¿¯ÂÛÎÄ, ÓÐЩӢÎĵ¥×ÖÔÚÒ»°ãÓ¢ÎÄ×Öµä²é²»µ½, ÐèÒªÓÃÓ¢ºº»¯Ñ§´Êµä, ÀýÈç menthol (±¡ºÉ´¼); ººÓ¢»¯Ñ§´ÊµäÔÚд×÷Ó¢ÎÄ»¯Ñ§ÂÛÎÄÊ±ÌØ±ðÐèÒª, Ò²Êdzö¹ú±Ø±¸, ÀýÈç¹²éî¶þÏ©µÄÓ¢ÎÄΪ conjugated diene. ½ÏÖøÃûµÄÓÐÒÔϼ¸ÖÖ°æ±¾:
        a. Ó¢ºº,ººÓ¢»¯Ñ§»¯¹¤´ó´Êµä (ѧԷ³ö°æÉç):  Ó¢ºººÍººÓ¢·Ö±ð±¨µ¼ 12ÍòºÍ14ÍòÌõÄ¿.
        b. Ó¢ºº,ººÓ¢»¯Ñ§»¯¹¤´Ê»ã (»¯Ñ§¹¤Òµ³ö°æÉç): ·ÖΪӢºººÍººÓ¢Á½¸öµ¥Ðб¾, ¸÷±¨µ¼ 8Íò¸öÌõÄ¿, Я´ø·½±ã.
        c.  Ó¢ºº»¯Ñ§»¯¹¤´Ê»ã (¿Æ¼¼³ö°æÉç): Áгö 17 ÍòÌõÄ¿, ±¨µ¼Ï꾡.
        ii). »¯ºÏÎïÃüÃû´Êµä  (ÉϺ£ÖñÊé³ö°æÉç): ½éÉÜ»¯ºÏÎïµÄÃüÃû¹æÔò,  ÓÐ 7000 ¶à¸öÀý×Ó, ÒÀÐò±¨µ¼ÎÞ»ú»¯ºÏÎï (Ò»Ôª, ¶þÔª, ¶àÔª»¯ºÏÎï, ÎÞ»úËáºÍÑÎ, Åäλ»¯ºÏÎï), Óлú»¯ºÏÎï (Ö¬·¾×å, ̼»·, ÔÓ»·, ÌìÈ»²úÎïÒÔ¼°º¬¸÷ÖÖ¹ÙÄÜ»ù»¯ºÏÎï) µÄÃüÃû½éÉÜ. ÿ¸ö»¯ºÏÎï¸ø½á¹¹Ê½¼°Í¬Òå´ÊµÄÖÐÓ¢ÎÄÃû×Ö. ÀýÈç C6H5OCH3 anisole (ÜîÏãÃÑ), methoxybenzene (¼×Ñõ»ù±½), methyl benzyl ether (±½¼×ÃÑ). ±¾´ÊµäË÷ÒýÆëÈ«, ÓзÖ×ÓʽË÷Òý, Ãû×ÖË÷Òý. Ãû×ÖË÷Òý°´ÕÕÖÐÎıʻ­ÅÅÐò, »ò°´ÕÕÖÐÎÄ»òÓ¢ÎÄÆ´ÒôÅÅÐò.

        (2). °²È«ÊÖ²á: ³õÈëʵÑéÊÒµÄѧÉúÒÔ¼°Ê×´ÎʹÓÃij»¯Ñ§Æ·µÄÈËÔ±Ó¦
Á˽âÇå³þʵÑéËùÉæ¼°µÄ»¯Ñ§Æ·µÄÐÔÖʼ°ÆäΣÏÕÖ¸±ê.
        i). ³£Óû¯Ñ§Î£ÏÕÎïÆ·°²È«ÊÖ²á (ÖйúÒ½Ò©¿Æ¼¼³ö°æÉç): ±¨µ¼Ô¼ 1000ÖÖʹÓÃ, Éú²ú, ÔËÊäÖÐ×î³£¼ûµÄ»¯Ñ§Ò©Æ·µÄ°²È«×ÊÁÏ. ±¨µ¼ÄÚÈÝÓÐ: »¯ºÏÎïµÄÀí»¯ÐÔÖÊ, ¶¾ÐÔ, °ü×°ÔËÊä·½·¨, ·À»¤´ëÊ©, й©´¦ÖÃ, ¼±¾È·½·¨ (ÀýÈçÆ¤·ô½Ó´¥äå, ÓÃË®³åÏ´10·ÖÖÓºóÔÙÓà 2% ̼ËáÇâÄÆÈÜÒº³åÏ´; ʳÈëäåÁ¢¼´Êþ¿Ú, ÒûÓÃÅ£Ä̼°µ°Çå). ±¾Êé°´ÕÕÖÐÎıʻ­ÅÅÐò, ¾íÄ©ÓÐÓ¢ÎÄË÷Òý, ÒÔ¼°ÖÐÓ¢¶ÔÕÕ, Ó¢ÖжÔÕÕË÷Òý.
        ii). »¯Ñ§Î£ÏÕÆ·×îÐÂʵÓÃÊÖ²á (ÖйúÎï×ʳö°æÉç): ±¨µ¼Ô¼ 1300 ÖÖ»¯Ñ§Ò©Æ·µÄÐÔ×´ (Íâ¹Û, ÆøÎ¶, ÈÛµã, ·Ðµã, ÉÁµã, ÃܶÈ, ÕÛÉäÂÊ), ΣÏÕÐÔ (¾ç¶¾, µÍ¶¾, Ö°©, ÓöË®ÊͷŶ¾Æø), ½û¼É (ÅÂË®, »ð, ¸ßÈÈ), Öü´æºÍÔËÊ䷽ʽ, й©´¦Àí, ·À»¤¼±¾È´ëÊ©µÈ.

        (3). °Ù¿ÆÈ«Êé, ´óÈ«, ÊÖ²á, Ŀ¼
        i). The Merck Index (Ĭ¿ËË÷Òý): Êǵ¹ú Merck ¹«Ë¾³ö°æµÄ·ÇÉÌÒµÐԵĻ¯Ñ§Ò©Æ·ÊÖ²á, Æä×Ô³ÆÊÇ ¡° »¯Ñ§Æ·, Ò©Æ·, ÉúÎïÊÔ¼Á°Ù¿ÆÈ«Ê顱. ±¨µ¼1ÍòÖÖ³£Óû¯Ñ§ºÍÉúÎïÊÔ¼ÁµÄ×ÊÁÏ. ÃèÊö¼ò½à, ×ÖÊýÊýÊ®ÖÁÊý°Ù, ÒÔÐðÊö·½Ê½½éÉܸû¯ºÏÎïµÄÎïÀí³£Êý (ÈÛµã, ·Ðµã, ÉÁµã, ÃܶÈ, ÕÛÉäÂÊ, ·Ö×Óʽ, ·Ö×ÓÁ¿, ±ÈÐý¹â¶È, Èܽâ¶È), ±ðÃû, ½á¹¹Ê½, ÓÃ;, ¶¾ÐÔ, ÖÆ±¸·½·¨ÒÔ¼°²Î¿¼ÎÄÏ×. Ĭ¿ËË÷ÒýÒѾ­³ÉΪ½éÉÜÓлú»¯ºÏÎïÊý¾ÝµÄ¾­µäÊÖ²á,  CRC, Aldrich µÈÊֲᶼÒýÓû¯ºÏÎïÔÚĬ¿ËË÷ÒýÖеıàºÅ.
ÊéµÄºó°ë²¿¼òµ¥½éÉÜÓÐÖøÃûµÄÓлúÃû³Æ·´Ó¦ (Name Reactions), ÀýÈç acyloin condensation, Knorr pyrrole synthesis, Curtiues rearrangement µÈ. ÊéÖп¯³öÐí¶à±í¸ñ, ±¨µ¼ÊµÓÃ×ÊÁÏ, ÀýÈçËõд, ·ÅÉäÐÔÍ¬Î»ËØº¬Á¿, Merck±àºÅÓë CA µÇ¼ÇºÅµÄ¶ÔÕÕ±í, ÖØÒª»¯Ñ§ÊÔ¼ÁÉú²ú¹«Ë¾µÈ. ±¾Êé±àÅŰ´ÕÕÓ¢ÎÄ×ÖĸÅÅÐò, ÊéÄ©ÓзÖ×Óʽ¼°Ãû×ÖË÷Òý.
        ii). Dictionary of Organic Compounds (Óлú»¯ºÏÎï×Öµä), ¼ò³Æ DOC, 1934 ÄêÊ×°æ, ÿ¼¸Äê³öÒ»ÐÞ¶©°æ, ÊÇÓлú»¯Ñ§, ÉúÎﻯѧ, Ò©Îﻯѧ¼ÒÖØÒªµÄ²Î¿¼Êé. ÄÚÈݺͺÍÅŰæÓë Merck Index ÀàËÆ, µ«ÊýÄ¿¶àÁ˽üÊ®±¶, ±¨µ¼10¶àÍòÖÖ»¯ºÏÎïµÄ×ÊÁÏ.  °´ÕÕÓ¢ÎÄ×ÖĸÅÅÐò, ÓÐÐí¶à·Ö²á, ¿¯ÔØ»¯ºÏÎïµÄ·Ö×Óʽ, ·Ö×ÓÁ¿, ±ðÃû, Àí»¯³£Êý (ÈÛµã, ·Ðµã, ÃܶȵÈ), ΣÏÕÖ¸±ê, ÓÃ;, ²Î¿¼ÎÄÏ×. ÒòΪÊýÄ¿ÅÓ´ó, ÁíÍâ³ö°æÓÐË÷Òý·Ö²á, °üÀ¨·Ö×ÓʽË÷Òý (ÀýÈç C5H13N, 2-Pentylamine, P-00561), CAµÇ¼ÇºÅ¶ÔÕÕË÷Òý (ÀýÈç 60-35-5, acetamide, A-00092), Ãû×ÖË÷Òý (ÀýÈç Bromoacetic acid, see B-01884).
        iii). Handbook of Chemistry and Physics (CRC »¯Ñ§ÎïÀíÊÖ²á), ¼ò³Æ CRC, ÊÇÃÀ¹ú»¯Ñ§Ï𽺹«Ë¾ (Chemical Rubber Company) ³ö°æµÄÀí»¯ÊÖ²á. 1913 ÄêÊ×°æ, ĿǰÒѳöµÚ 79 °æ±¾ (1999 Äê). ÔçÆÚ (ÀýÈçµÚ63 °æ) ÄÚÈÝ·ÖΪ6´óÀà, ±¨µ¼ÊýѧÓñí, ÎÞ»ú, Óлú, ÆÕ»¯, ÆÕͨÎïÀí³£Êý, ¼°ÆäËü. ĿǰÀ©³ä±¨µ¼14 ²¿, °üÀ¨»ù±¾³£Êýµ¥Î» (section 1), ·ûºÅºÍÃüÃû (section 2), Óлú (section 3), ÎÞ»ú (section 4), ÈÈÁ¦Ñ§¶¯Á¦Ñ§ (section 5), Á÷Ìå (section 6), Éú»¯ (section 7), ·ÖÎö (section 8) µÈ. ÆäÖеÚ3²¿µÄÓлú»¯Ñ§±¨µ¼Õ¼ 740 Ò³, Óñí¸ñºÜ¼òÂԵĽéÉÜ 12000 ÖÖ»¯ºÏÎïµÄÀí»¯×ÊÁÏ (ÀýÈç·Ö×ÓÁ¿, ÈÛµã, ·Ðµã, ÃܶÈ, ÕÛÉäÂÊ, Èܽâ¶È), ÒÔ¼°±ðÃû, Merck index ±àºÅ,  CAS µÇ¼ÇºÅ, ¼°ÔÚBeilstein µÄ²Î¿¼ÊéÄ¿ (Beil. Ref) µÈ. Beilstein ²Î¿¼ÊéÄ¿µÄд·¨ÔçÆÚΪ B84, 252, аæ¸ÄΪ 4-08-00-00252,  ´ú±íÔÚBeilstein µÚ4ϵÁÐ (²¹Æª)µÚ8¾í252Ò³ (аæµÄ 00 ±í¸½¾í). »¯ºÏÎïµÄÃû×ÖÅÅÐò·ÂÕÕÃÀ¹ú»¯Ñ§ÎÄÕª, ÒÔĸÌ廯ºÏÎïΪÖ÷, ÀýÈç p-bromoaniline (¶Ôäå±½°·) ²é·¨Îª Benzenamine, 4-bromo.
½ô½Ó×űí¸ñ, ¿¯³öÓÐÒÔÉÏ1Íò¶àÖÖ»¯ºÏÎïµÄ½á¹¹Ê½. ±¾ÕºóÃæµÄË÷ÒýÓÐͬÒå´ÊË÷Òý, CAS µÇ¼ÇºÅË÷ÒýµÈ.
CRC ÊǸö¶àÓÃ;µÄÊÖ²á, ÆäËüÕ½ڱ¨µ¼ÓпƼ¼Ãû´ÊµÄ¶¨Òå, ÃüÃû¹æÔò, Êýѧ¹«Ê½, »¹ÓÐÐí¶à±í¸ñ¿¯ÔØÀýÈçÕôÆûѹ, ÓÎÀëÄÜ, ¼ü½Ç¼ü³¤µÈÓÐÓõÄ×ÊÁÏ.ÔçÆÚµÄ CRC Óлú²¿·ÖÓÐÈÛµã (-197 - 913 ¡ãC) ºÍ·ÐµãË÷Òý (-164 - 891 ¡ãC), ¿ÉÒÔ´ÓÈÛµã·ÐµãÊý¾Ý²é³ö¿ÉÄܵϝºÏÎï½á¹¹.  CRC ¸ù¾Ý International System of Units, Symbols and Terminology for Physical and Chemical Quantities, Definitions of Scientific Term System µÄ¹æ¶¨, ÁгöÁËÊé°Ù¸ö¹ú¼Ê³ÐÈϵĵ¥Î», ·ûºÅ, Ãû³ÆµÄËõд.
        iv). Lange¡¯s Handbook of Chemistry (À¼ÊÏ»¯Ñ§ÊÖ²á): ÄÚÈÝºÍ CRC ÀàËÆ, ·Ö11Õ·ֱ𱨵¼Óлú, ÎÞ»ú, ·ÖÎö, µç»¯Ñ§, ÈÈÁ¦Ñ§µÈÀí»¯×ÊÁÏ. ÆäÖÐµÚÆßÕ±¨µ¼Óлú»¯Ñ§, ¿¯ÔØ 7600 ÖÖÓлú»¯ºÏÎïµÄµÄÃû³Æ, ·Ö×Óʽ, ·Ö×ÓÁ¿, ÈÛµã, ·Ðµã, ÉÁµã, ÃܶÈ, ÕÛÉäÂÊ, Èܽâ¶È, ÔÚBeilstein µÄ²Î¿¼ÊéÄ¿µÈ. ÆäËüÕ½ڱ¨µ¼Óнéµç³£Êý, ż¼«¾æ, ºË´ÅÇâÆ×̼Æ×»¯Ñ§Î»ÒÆ, ¹²·ÐÎïµÄ·ÐµãºÍ×é³ÉµÈÓÐÓõÄ×ÊÁÏ. ±¾ÊÖ²áÓÐÖÐÎÄ·­Òë±¾³ö°æ.
        v). Beilstein  Handbuch der Organischen Chemie (±´¶û˹̹Óлú»¯Ñ§´óÈ«): ¼ò³Æ Beilstein,  ÎªµÂ¹ú»¯Ñ§¼Ò Beilstein ±àд, 1882 ÄêÊ×°æ, Ö®ºóÓɵ¹ú»¯Ñ§»á±à¼­, ÒÔµÂÎÄÊéд, ÊDZ¨µ¼Óлú»¯ºÏÎïÊý¾ÝºÍ×ÊÁÏÊ®·ÖȨÍþµÄ¾ÞÖø. ÄÚÈݽéÉÜ»¯ºÏÎïµÄ½á¹¹, Àí»¯ÐÔÖÊ, ÑÜÉúÎïµÄÐÔÖÊ, ¼ø¶¨·ÖÎö·½·¨, ÌáÈ¡´¿»¯»òÖÆ±¸·½·¨ÒÔ¼°Ô­Ê¼²Î¿¼ÎÄÏ×. Beilstein Ëù±¨µ¼»¯ºÏÎïµÄÖÆ±¸ÓÐÐí¶à±ÈԭʼÎÄÏ×»¹Ï꾡, ²¢ÇÒ¸üÕýÁËÔ­×÷ÕߵĴíÎó. ËäÈ»µÂÎIJ»ÈçÓ¢ÎÄÆÕ±é, µ«ÊÇÐí¶àÔçÆÚµÄ»¯Ñ§×ÊÁÏÈÔÐè½èÖú Beilstein²éѯ, ¼ÓÉÏĿǰ Beilstein Onlin ÍøÂçµÄÁ÷ÐÐ (¼Û¸ñ±È CA ±ãÒ˹ãÓÃ), Òò´ËѧϰºÍÁ˽â Beilstein µÄ±à¼­ºÍʹÓ÷½·¨ÈÔÊDz»¿ÉÃâµÄ.
        Beilstein Ŀǰ³ö°æÓÐ 7 ´óϵÁÐ( H, E I, E II, E III, E III/IV, E IV, E V), ÆäÖÐ H ±í Hauptwerk (Õý±à), E ±í Erganzungswerk (²¹±à). H ϵÁÐΪ»ù±¾ÏµÁÐ (Basic Series), ±¨µ¼ 1910 ÄêÒÔǰµÄÎÄÏ××ÊÁÏ, Ö®ºóÿ10ÄêÔö¼ÓÒ»¸öϵÁÐ (²¹Æª). ºóÃæµÄ²¹±àÖð½¥²ÉÓÃÓ¢ÎÄÊéд. ÿ¸öϵÁÐÓÐ27 ¾íÖ÷¾í (ÆäËüΪË÷Òý), ºáÏò·ÖΪÈý´ó²¿·Ö: Acyclics (·Ç»·Ïµ, 1-4 ¾í), Isocyclics (̼»·×å, 5-6 ¾í), Heterocyclics (ÔÓ»·»¯ºÏÎï, 7-27 ¾í). °´ÕÕËù¾ßÓеĹÙÄÜ»ù×ÝÏòÒÀÐò·ÖΪ: ÎÞ, OH, C=O, CO2H, SO3H, Se, NH2, NHOH, ½ðÊôÓлúµÈ17Àà; ÓÐ "Table of Contents of the 27 Volumes of the Beilstein Handbook" °ïÖúÁ˽âÉÏÊö·ÖÀà. Èç¹ûÄÜÓÉ·Ö×ÓʽË÷ÒýµÃµ½»¯ºÏÎï, ±ãÄÜÖ±½ÓÕÒµ½ÆäÔÚÊé¾íÖеÄλÖÃ. ´Ó CRC , Lange's Handbook »ò Merck Index Öеõ½µÄ Beil. ref Ò²Êǽݾ¶, Àý×ÓÈç B72, 243 ´ú±í¸Ã»¯ºÏÎï³öÏÖÔÚ Beilstein µÚ2 ϵÁÐ (²¹Æª)µÚ7¾í243Ò³. Beilstein µÄË÷Òý²»¹»ÆëÈ«, Òò´Ë²éÔÄ×ÊÁÏÐèÒªÁ˽âÆä±àÅÅ·½Ê½ÒÔÅж¨Ëù²é»¯ºÏÎïµÄλÖÃ. Beilstein µÄ±àºÅÓÐÒ»ÌØµã, »¯ºÏÎïµÄ¾íºÅ¿ÉÒÔºÍÆäËüϵÁÐͨÓÃ.  Beilstein »¹ÓÐÖ÷ÌâË÷Òý, ±È·Ö×ÓʽË÷ÒýʵÓú͹ãÓÃ, ÓÃÀ´²éÕÒĸÌå½á¹¹»¯ºÏÎï.
        vi). ÉÌÓÃÊÔ¼ÁĿ¼: ÓŵãΪĿ¼Ãâ·ÑË÷È¡, ÿÄê¸üÐÂ, ÓÃÀ´²éÔÄ»¯ºÏÎïµÄ»ù±¾Êý¾Ý (·Ö×ÓÁ¿, ½á¹¹Ê½, ·Ðµã, ÈÛµã, ÃüÃûµÈ) Ê®·Ö·½±ãʵÓÃ. ÕâЩÉÌÓÃÊÔ¼ÁĿ¼´óСÊÊÖÐ, ÔÚ¹úÍâʵÑéÊÒÈËÊÖÒ»²á, ±»µ±×ö»¯Ñ§×Öµä»òÊý¾ÝÊÖ²áʹÓÃ, Ò²ÊǺܺõĻ¯Ñ§²úÆ·¹ºÎïÖ¸ÄÏ. Ŀ¼Öл¯ºÏÎïµÄ¼Û¸ñ¿ÉÒÔ×öΪʵÑéÉè¼ÆµÄÖØÓòο¼. Ŀ¼Öл¹Ìṩ²Î¿¼ÎÄÏ×, ¹âÆ×À´Ô´, ¶¾ÐÔ½éÉܵÈ. ±È½ÏÖøÃûµÄÉÌÓÃÊÔ¼ÁĿ¼ÓÐÒÔϼ¸ÖÖ:
        a. Aldrich: È«ÃûΪ Aldrich Catalog Handbook of Fine Chemicals, ÃÀ¹ú Aldrich ¹«Ë¾³ö°æ, ×ܲ¿ÉèÔÚ Wisconsin ÖÝ Milwarkee. ÔÚÃÀ¹úÑо¿ÊÒÈËÊÖÒ»²á. ±¾Ä¿Â¼±¨µ¼ 37000 ÖÖ»¯Ñ§Æ·µÄÀí»¯³£ÊýºÍ¼Û¸ñ, ±àÅżò½à. ³ýÁË»¯Ñ§ÊÔ¼Á, Ò²¿¯ÔغͳöÊÛ¸÷ÖÖʵÑéÉ豸ÀýÈç²£Á§ÒÇÆ÷, »¯Ñ§Êé¼®, ÒDZíµÈ; ÓÐÏêϸ¸½Í¼ºÍ¹¦ÄÜ˵Ã÷, ÊDZ¾ºÜºÃµÄ¹ºÎïÖ¸ÄÏ, ¿ÉÒÔ½èÓÉͼÎĽéÉÜÁ˽⻯ѧÒÇÆ÷µÄÓÃ;»òÆäÓ¢ÎÄÃû³Æ.
        b. Acros: Å·ÖÞ³ö°æµÄÊÔ¼ÁĿ¼, ĿǰÔÚ¹úÄÚÁ÷ÐÐ. Òò¹©»õÆÚ¶Ì (2-4 ÖÜ), ¶©¹º»¯ºÏÎï·½±ã, ¹©Ó¦ÊµÑéÊÒһЩ¹úÄÚÂò²»µ½µÄÊÔ¼Á.
        c. Sigma: È«ÃûΪ Sigma Biochemical and Organic Compounds for Research and Diagnostic Clinical Reagents, Ö÷ÒªÌṩÉú»¯ÊÔ¼Á²úÆ·. ×ܲ¿ÔÚÃÀ¹ú Missouri ÖÝ St. Louis.
        d. Fulka: ×ܲ¿ÔÚÈðµä, Fluka »¯Ñ§¹«Ë¾. Æä²úÆ·ÓÐЩÊÇ Aldrich ÕÒ²»µ½µÄ.
        e. Merck Catalogue: µÂ¹ú Merck ¹«Ë¾µÄÉÌÆ·Ä¿Â¼, °üÀ¨ÓÐ 8000 ÖÖ»¯Ñ§ºÍÉúÎïÊÔ¼Á, ¼°ÊµÑéÉ豸.

        (4). Óлú»¯Ñ§´ÓÊé, ʵÑ鸨Öú²Î¿¼Êé:
        i). Organic Reactions (Óлú·´Ó¦): ÊÇÒ»Ì×½éÉÜÖøÃûÓлú·´Ó¦µÄ×ÛÊö´ÔÊé, 1942 ÄêÊ×°æ, ÿ1-2 Äê³ö°æÒ»ÆÚ, ĿǰÒѾ­ 40¼¸ÆÚ. ÿÆÚ¶¼»áÁгöÒÔǰ¼¸ÆÚµÄĿ¼ºÍ×ÛºÏË÷Òý. ¸å¼þÎªÌØÑû¸å, ×ÛÊö½éÉÜÒ»Ð©ÖøÃûµÄ·´Ó¦, ÌâÄ¿ÀýÈç: The Cannizzaro Reaction (2-3,  µÚ¶þÆÚµÚÈýÕÂ), The Michael Reaction (10-3), The Beckmann Rearrangement (11-1), The Intramolecular Diels-Alder Reaction (21-1), Reduction with diimide (40-2) µÈ. ÄÚÈÝÃèÊö¼«ÎªÏ꾡, °üÀ¨Ç°ÑÔÀúÊ·½éÉÜ, ·´Ó¦»úÀí, ¸÷ÖÖ·´Ó¦ÀàÐÍ, Ó¦Ó÷¶Î§ºÍÏÞÖÆ, ·´Ó¦Ìõ¼þºÍ²Ù×÷³ÌÐò, ×ܽá. ÿÕÂÓÐÐí¶à±í¸ñ¿¯Ôظ÷ÖÖÑо¿¹ýµÄ·´Ó¦ÊµÀý, ¸½ÓдóÁ¿µÄ²Î¿¼ÎÄÏ×.  ¹úÍâÓлú¿Î³Ì¾­³£ÒÔ´ËÊé×öΪ¿ÎÍâ×÷Òµ, ÈÃѧÉú²éÔĺÍÃèдij·´Ó¦µÄÄÚÈÝ, »úÀíºÍÓ¦Ó÷¶Î§.
        ii). Organic Synthesis (ÓлúºÏ³É): ÊÇÒ»Ì×Ïêϸ½éÉÜÓлúºÏ³É·´Ó¦²Ù×÷²½ÖèµÄ´ÔÊé. ÄÚÈÝ¿ÉÐŶȼ«¸ß, ÿ¸ö·´Ó¦¶¼¾­¹ýÖÁÉÙÁ½¸öʵÑéÊÒÖØ¸´Í¨¹ý. ×îÒýÈËÈëʤµÄÊǺóÃæµÄ Notes, Ïêϸ˵Ã÷²Ù×÷ʱӦ¸Ã×¢ÒâÊÂÏî¼°½âÊÍΪºÎÈç´ËÉè¼Æ, ²»µ±²Ù×÷¿ÉÄܵ¼Öµĸ±²úÎïµÈ. ÊDZ¾Ñ§Ï° “know how¡± µÄ·´Ó¦´ÔÊé.
        iii). Reagents for Organic Synthesis (ÓлúºÏ³ÉÊÔ¼Á): Fieser & Fieser Ö÷±à, 1967 Äê³ö°æµÄϵÁдÔÊé, ÿ 1-2 Äê³ö°æÒ»ÆÚ. ÆäǰÉíÊÇ Expeirments in Organic Chemistry (Óлú»¯Ñ§ÊµÑé). ÿÆÚ½éÉÜÕâ1-2 ÄêÆÚ¼äһЩ½ÏÌØÊâµÄ»¯Ñ§ÊÔ¼ÁËùÉæ¼°µÄ»¯Ñ§·´Ó¦.  ÀýÈç Butyllithium, Trifuloroacetic acid,  Ferric chloride »ò×îз¢Ã÷µÄÊÔ¼Á. ¿ÉÒÔ´ÓË÷Òý²éÔÄÊÔ¼ÁÃû×Ö, ת¶ø²éÕÒÆä·´Ó¦Ó¦ÓÃ. ÿ¸ö·´Ó¦¶¼ÓÐÏêϸµÄ²Î¿¼ÊéÄ¿.
        iv). Vogel ¡®s textbook of Practical Organic Chemistry¡±, ¼ò³Æ Vogel. 1948 ÄêÊ×°æ, ÊÇÒ»±¾Ê®·ÖʵÓõķ´Ó¦²Î¿¼Êé, ¹úÍâÿ¸öÑо¿×é¶¼ÓÐÒ»±¾ÖÃÓÚÊé¼Ü. ¿ÉÒԲο¼¹éÄÉÊéÖнéÉܵÄÐí¶àÀàËÆ·´Ó¦À´Éè¼ÆÎ´ÖªµÄ·´Ó¦Ìõ¼þ. ÄÚÈÝÖ÷Òª°´ÕÕ¹ÙÄÜÍÅ¿¯ÔØ·´Ó¦. Èçͬ±¾¿ÆÉúµÄʵÑé½Ì²ÄÒ»°ã, ±¾Êé¶ÔÓÚ·´Ó¦Ìõ¼þºÍ²Ù×÷³ÌÐòÃèÊöµÃÊ®·ÖÇå³þ, ÓÐÐí¶à·´Ó¦ÊµÀýºÍÆä²Î¿¼ÎÄÏ×. ÊéÄ©¿¯ÔØ»¯ºÏÎïµÄÀí»¯³£Êý, ºÍ CRC µÈÆäËü»¯Ñ§Êֲ᲻ͬµÄÊDZ¾Êé°´ÕÕ¹ÙÄÜÍÅÅÅÐò, Òò´ËÄÜͬʱÁгö¸Ã»¯ºÏÎïÑÜÉúÎïµÄÈÛµã»ò·ÐµãÊý¾Ý. ÊéµÄÇ°Ãæ¼¸Õ½éÉÜʵÑé²Ù×÷¼¼Êõ. ¸½Â¼Óи÷ÖÖ¹ÙÄÜÍŵĹâÆ×½éÉÜ, ÀýÈçºìÍâÎüÊÕλÖÃ, ºË´ÅÇâÆ×ºÍ̼Æ×µÄ»¯Ñ§Î»ÒƵÈ.
        v). Purification of Laboratory Chemicals (ʵÑéÊÒ»¯ºÏÎïµÄ´¿»¯): Perrin µÈÖ÷±à. ÕâÊÇʵÑéÊÒÖо­³£Ê¹Óõ½µÄ²Î¿¼Êé¼®. ÄÚÈݱ¨µ¼¸÷ÖÖ»¯ºÏÎïµÄ´¿»¯·½·¨, ÀýÈçÖØ½á¾§µÄÈܼÁÑ¡Ôñ, ³£Ñ¹ºÍ¼õѹÕôÁóµÄ·Ðµã, ÒÔ¼°´¿»¯ÒÔǰµÄ´¦ÀíÊÖÐøµÈ. ´Ó´ÖÂÔ´¿»¯µ½¸ß¶È´¿»¯¶¼ÓÐÏêϸ±¨µ¼, ²¢¸½²Î¿¼ÎÄÏ×. ǰ¼¸Õ½éÉÜÌá´¿Ïà¹Ø¼¼Êõ (ÖØ½á¾§, ¸ÉÔï, É«Æ×, ÕôÁó, ÝÍÈ¡µÈ), »¹ÓÐÐí¶àʵÓõıí¸ñ, ½éÉÜÀýÈç¸ÉÔï¼ÁµÄÐÔÖʺÍʹÓ÷¶Î§, ²»Í¬Î¶ȵÄÔ¡²ÛµÄÖÆ±¸, ³£ÓÃÈܼÁµÄ·Ðµã¼°»¥ÈÜÐÔµÈ×ÊÁÏ.
        vi). Chemical Reviews (»¯Ñ§×ÛÊö):  ÃÀ¹ú»¯Ñ§»áÖ÷°ì, 1924 Äê´´¿¯, Ò»Äê³ö°æ8ÆÚ, ÎªÌØÑû¸å. Ó°ÏìÒò×ÓΪ17.1, ±ÈÒ»°ãÆÚ¿¯¸ß½üÊ®±¶, ¿É¼ûÆäÊÜ»¶Ó­ºÍÖØÊӵij̶È. ×ÛÊöÎÄÏ×µÄÓŵãÔÚÓÚ¿ÉÒÔ´Ó¸÷¸ö½Ç¶È³ä·ÖÁ˽ⱨµ¼µÄרÌâ, ÎÄÏ׺óÃæ¸½ÓдóÁ¿µÄ²Î¿¼ÎÄÏ×, ÓÐÀûÓÚԭʼ×ÊÁϵIJéÔÄ. ±¨µ¼µÄרÌâÀýÈç: Chromatography (1989), Reactive Intermediate (1991), Boron Chemistry (1992), Photochemistry (1993), Heterogeneous Catalysis (1995), Combinatorial Chemistry (1997). ÎÄÕÂÄÚÈݰüÀ¨ÓÐǰÑÔÀúÊ·½éÉÜ, ¸÷ÖÖ·´Ó¦ÀàÐͼ°Ó¦ÓÃ, ½áÂÛºÍδÀ´Ç°¾°.
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ľ³æ (ÕýʽдÊÖ)

(¶þ). ¶þ´ÎÎÄÏ×:
ÃÀ¹ú»¯Ñ§ÎÄÕª (Chemical Abstracts): ¼ò³Æ CA, ÃÀ¹ú»¯Ñ§»áÖ÷°ì, 1907 Äê´´¿¯, ÊÇĿǰ±¨µ¼»¯Ñ§ÎÄÕª×îÓÆ¾Ã×îÆëÈ«µÄ¿¯Îï. ±¨µ¼·¶Î§º¬¸ÇÊÀ½ç160 ¶à¸ö¹ú¼Ò 60 ¶àÖÖÎÄ×Ö, 17000 ¶àÖÖ»¯Ñ§¼°»¯Ñ§Ïà¹ØÆÚ¿¯µÄÎÄÕª. ÿÖܳö°æÒ»ÆÚ, Ò»Äê¹²±¨µ¼70 ÍòÌõ»¯Ñ§ÎÄÕª, ռȫÇò»¯Ñ§ÎÄÏ×µÄ 98 %.
ÿһÆÚ°´ÕÕ»¯Ñ§×¨Òµ·ÖΪ 5 ´ó²¿ 80 Àà: Éú»¯ (1-20 Àà), Óлú (21-34), ´ó·Ö×Ó (35-45), Ó¦Óû¯Ñ§ºÍ»¯¹¤ (47-64), ÎﻯÎÞ»ú·ÖÎö (65-80). Óлú²¿ÃŵÄÀý×ÓÈçÎïÀíÓлú»¯Ñ§ (22), Ö¬·¾×廯ºÏÎï (23), Ö¬»·×廯ºÏÎï (24),  ¶àÔÓÔ­×ÓÔÓ»·»¯ºÏÎï (28), Óлú½ðÊô (29), çÞ×廯ºÏÎï (32), °±»ùËáºÍµ°°×ÖÊ (34). ÿһÆÚµÄ»¯Ñ§ÎÄÕª¿ÉÒÔµ±×öͼÊéÔĶÁ, ÀýÈçÎïÀíÓлú»òÓлú½ðÊôרҵµÄÑо¿ÈËÔ±, ¿ÉÒÔ¶¨ÆÚÔĶÁÿÆÚµÚ22Àà»ò29ÀàµÄÎÄÕª, ºÜÈÝÒ׵ıã¿ÉÁ˽âÕâÒ»ÖÜÖÐÊÀ½çÖ÷Òª»¯Ñ§ÆÚ¿¯, »áÒé¼, ¿Æ¼¼±¨¸æ, ѧλÂÛÎÄ, ÐÂÊé, רÀû (ÒÔÉÏΪ CA ¿¯ÔصĿ¯ÎïÀà±ð) ±¨µ¼ÕâЩÁìÓòµÄ¿ÆÑÐ×ÊÁÏ.
ÓÉÓÚÎÄÕªÊýÁ¿ÅÓ´ó, CA Éè¼ÆºÍ³ö°æÁËÐí¶à²»Í¬ÐÎʽµÄË÷Òý, °´ÕÕʱ¼äÇø·ÖÓÐÆÚË÷Òý (Ò»ÖÜ), ¾íË÷Òý (ÿ26ÆÚ), ÀÛ»ýË÷Òý (ÿ10¾í, Ô¼5Äê) ÈýÖÖ; °´ÕÕÄÚÈÝÇø·ÖÓйؼü´ÊË÷Òý (keyword index), ×÷ÕßË÷Òý (author index), רÀûË÷Òý (patent index), Ö÷ÌâË÷Òý (subject index), ÆÕͨÖ÷ÌâË÷Òý (general subject index), »¯Ñ§ÎïÖÊË÷Òý (chemical substance index), ·Ö×ÓʽË÷Òý (formula index), »·ÏµË÷Òý (index of ring system), µÇ¼ÇºÅË÷Òý (registry number index), ĸÌ廯ºÏÎïË÷Òý (parent compound index). ÒÔ¼°Ë÷ÒýÖ¸ÄÏ (index guide), ×ÊÁÏÀ´Ô´Ë÷Òý (CAS source index) µÈ. ÿÖÖË÷ÒýµÄʹÓ÷½·¨¿ÉÒÔ²ÎÔÄÿÆÚ, ÿ¾í»òÿÀÛ»ý±¾µÄµÚÒ»±¾Ç°ÃæµÄ·¶Àý˵Ã÷.        
CA ³ýÁË×öΪͼÊéÎÄÕªÔĶÁ, ÆäÖ÷Òª¹¦ÓÃÔÚÓÚ²éÕÒÎÄÏ××ÊÁÏ, ÀýÈç: ²éij¸ö»¯ºÏÎïµÄԭʼ±¨µ¼ (¿ÉÒÔ´Ó·Ö×ÓʽË÷Òý, µÇ¼ÇºÅË÷Òý, »·ÏµË÷ÒýµÈ×ÅÊÖ) , ²éij¸ö»¯Ñ§·´Ó¦ (»¯Ñ§ÎïÖÊË÷Òý), ²éijÈ˽üÄêÀ´µÄ¿ÆÑÐÇéÐÎ (×÷ÕßË÷Òý), ²éijÏîרÀûÄÚÈÝ (רÀûË÷Òý). ʵÀýÈç²éÕÒ¶Ô¼×±½·ÓºÍÏ©µÄ¼Ó³É·´Ó¦: ¿ÉÒÔ´Ó»¯Ñ§ÎïÖÊË÷Òý×ÅÊÖ, ÕÒµ½ p-cresol ºóÓÉ reaction ¸±±êÌâÕÒºÍÏ©ÌþµÄ·´Ó¦, µÃµ½ÎÄÕªºÅºóÔĶÁÎÄÕª, Èç¹û¶ÔÄÚÈÝÂúÒâ, ÓÉÆäÌṩµÄ×ÊÁÏÕÒѰԭʼÎÄÏ×. ½øÒ»²½, µÃµ½ÎÄÕºÍ×÷Õß Saha, M. ºó, ¿ÉÒÔ´Ó×÷ÕßË÷Òý×·²éÆäËùÑо¿µÄÍêÕûϵÁÐ.
¹úÄÚĿǰÒÑ´ÓÃÀ¹ú»¯Ñ§ÎÄÕª·þÎñÉ繺Èë1992 ÄêÒÔºóµÄÀÛ»ý»ò¾íË÷Òý¼°ÎÄÕªµÄ¹âÅÌ (CA on CD), ¿ÉÒÔÁª»ú¼ìË÷.

        (Èý). Ò»´ÎÎÄÏ×:
        (1). ¹úÍ⻯ѧÆÚ¿¯
        i). ÃÀ¹ú³ö°æµÄ»¯Ñ§ÆÚ¿¯
a. The Journal of the American Chemical Society (ÃÀ¹ú»¯Ñ§»áÖ¾): ¼òдΪ J. Am. Chem. Soc.,  ÊÇĿǰ»¯Ñ§ÆÚ¿¯Öм¶±ð½Ï¸ßµÄ, Ó°ÏìÒò×Ó 5.9. ±¨µ¼×ۺϻ¯Ñ§ (Óлú, ÎÞ»ú, ·ÖÎö, ÎﻯµÈ), ÄÚÈÝÓг¤ÆªÂÛÎÄºÍ¶ÌÆª¼ò±¨ (1-2 Ò³, Communication to the Editors) ¸÷Ê®ÓàÆª, ²Î¿¼ÎÄÏ׳öÏÖÔÚÿҳÎÄÕÂÏÂÃæ, Èç´ËÖøÃûµÄÆÚ¿¯µ½Ä¿Ç°È´»¹Ã»ÓÐÖÆ×÷ͼÎÄÕªÒª (graphic abstract). ÔÚͼÊé¹ÝµÄ°ÚÉè, ÓÐЩ´Ó J, ÓÐЩ´Ó T (ÀýÈçĿǰ±±´óͼÊé¹ÝÏÖ¿¯ÊÒ), Ò²ÓÐЩ´Ó A.
        b. The Journal of Organic Chemistry (Óлú»¯Ñ§»áÖ¾), ¼òдΪ J. Org. Chem., ÃÀ¹ú»¯Ñ§Ñ§»áÖ÷°ì, Ë«ÖÜ¿¯, ×ܲ¿ÔÚ Ohio State University, Ó°ÏìÒò×Ó 3.7. ±¨µ¼ÓлúºÍÉúÎïÓлú»¯Ñ§·½ÃæµÄÂÛÎÄ, Óг¤ÆªµÄ articles ÒÔ¼°½Ï¶ÌƪµÄ notes ºÍ communications. ÎÄÏ×ÌâÄ¿×ö³ÉͼÎÄÕªÒª (graphic abstract) ·½±ãÁ˽âÎÄÕÂÄÚÈÝ.
        ii). Ó¢¹ú³ö°æµÄ»¯Ñ§ÆÚ¿¯:
        a. Journal of the Chemical Society (Ó¢¹ú»¯Ñ§»áÖ¾), ¼ò³Æ J. Chem. Soc., Ó¢¹ú»Ê¼Ò»¯Ñ§Ñ§»áÖ÷°ì, 1848 Äê´´¿¯, ÊÇ×îÀϵĻ¯Ñ§ÆÚ¿¯. 1976 ÄêÆð·Ö³ÉÏÂÃæ¼¸¸ö²¿·Ö:
        1.. J. Chem. Soc. Perkin Transactions I: ±¨µ¼ÓлúºÍÉúÎïÓлú»¯Ñ§ÁìÓòµÄºÏ³É·´Ó¦. ÎÄÏ×ÄÚÈݱȽϳ¤, ±¾ÆÚ¿¯²»½ÓÊÜÃ÷ÏÔ½«ÍêÕûÎÄÕ·ֶÎͶ¸åµÄÇéÐÎ. Ó°ÏìÒò×Ó 1.6.
        2. J. Chem. Soc. Perkin Transactions II: ÎïÀíÓлúÁìÓò, ±¨µ¼Óлú, ÉúÎïÓлú, Óлú½ðÊô»¯Ñ§·½ÃæµÄ·´Ó¦»úÀí, ¶¯Á¦Ñ§, ¹âÆ×¼°½á¹¹·ÖÎöµÈÎÄÕÂ. Ó°ÏìÒò×Ó 1.7.
        3. J. Chem. Soc.Faraday Transactions: ÎïÀí»¯Ñ§ºÍ»¯Ñ§ÎïÀíÁìÓò, ±¨µ¼¶¯Á¦Ñ§, ÈÈÁ¦Ñ§ÎÄÕÂ.
        4. J. Chem. Soc. Dalton Transactions: ÎÞ»ú»¯Ñ§ÁìÓò.
        5. J. Chem. Soc. Chemical Communication: Ϊ°ëÔ¿¯, ÄÚÈݼò¶Ì, ²»³¬¹ýÁ½Ò³, ûÓÐǰÑÔÌÖÂÛ½áÂÛ, ƽÆÌÖ±Ðð¶ø¼ò½àµÄ½éÉÜʵÑéеĽøÕ¹»ò·¢ÏÖ. Ó°ÏìÒò×Ó 3.1.
        b. Tetrahedron (ËÄÃæÌå): 1957 Äê´´¿¯, °ëÔ¿¯, Óлú»¯Ñ§ÁìÓò, ¿¯ÔØÓлú·´Ó¦, ¹âÆ×ºÍÌìÈ»²úÎï. Ó°ÏìÒò×Ó 2.1.
        c. Tetrahedron Letters (ËÄÃæÌå¿ì±¨): 1959 Äê´´¿¯, ÖÜ¿¯. ÎÄÕÂÄÚÈݼò½à, Ò»°ã2-4 Ò³, Ó°ÏìÒò×Ó2.3. ±¾ÆÚ¿¯ºÍËÄÃæÌåÔÚÖйúµØÇøµÄÉó¸åÓÉÉϺ£ÓлúËù¸ºÔð. ¿ì±¨µÄÎÄÕ·¢±íºó½«À´¿ÉÒÔ×éºÏ³É´óÎÄÕÂÖØÐ·¢±í.
        iii). ±¨µ¼ÔÓ»·»¯ºÏÎïµÄÆÚ¿¯
a. Journal of Heterocyclic Chemistry (ÔÓ»·»¯Ñ§ÔÓÖ¾): 1964 Äê´´¿¯, ˫Կ¯, ±¨µ¼ÔÓ»·»¯Ñ§·½ÃæµÄ³¤ÆªÂÛÎĽü30 ƪ, ¼òѶ3-5 ƪ. ÿÄêµÄ×îÄ©ÆÚ¿¯³öÈ«ÄêµÄË÷Òý, ÓÐ×÷ÕßË÷Òý (author index) ºÍ»·ÏµË÷Òý (ring index).  
b. Heterocycles (ÔÓ»·»¯ºÏÎï): ÈÕ±¾³ö°æ, À¸Ä¿Éú¶¯, ÓÐͨѶ, ÂÛÎÄ, ×ÛÊö, ÒÔ¼°½üÄêз¢ÏÖµÄÔÓ»·ÌìÈ»²úÎï (·ÖÝÆ, ¹Ì´¼µÈ6Àà), ½üÄê½øÐÐÈ«ºÏ³É̽ÌÖµÄÌìÈ»²úÎï. ºó¶þÕß²¢¸½ÓÐÆÚ¿¯³ö´¦.
        iv).  µÂ¹ú³ö°æµÄ»¯Ñ§ÆÚ¿¯:
a. Synthesis (ºÏ³É): ÒÔÓ¢ÎÄÊéд, ×ÅÖØ·´Ó¦ºÏ³É±¨µ¼, Ê®·ÖÏêϸ, ²»·¦ÊýʮҳµÄÎÄÕÂ, µ«¿¯Ó¡³öÀ´µÄ±È½Ï¼ò½à, Ö»ÓÐÖ÷ÒªÄÚÈÝ´óÒâ. ¶øÍêÕûµÄ²¿·ÖµÃ´Ó΢Ëõ½ºÆ¬µ÷ÔÄ, ²»Áí³öÊé. ÊDZ¾ÆÚ¿¯µÄÌØµã.
b. Angewandte Chemie International Edition in English: 1965 Äê³ö°æ, ÊǵÂÎİæ Angewandte Chemie µÄÓ¢ÎÄ·­Òë°æ, ¶þÕß±¨µ¼µÄÄÚÈÝÏàͬ. À¸Ä¿ÓÐ reviews, highlight ÒÔ¼° communications. ÆäÖÐ highlight ÀàËÆÐ¡ÐÍ×ÛÊö, ÃèÊöij¸ö±È½ÏÉú¶¯µÄ¿ÎÌâ. ÍøÂç²éѯ, ÍøÖ·Îª: www.wiley.vch.de/home/angewandte
c. Angewandte Chemie: ÄÚÈÝÓëÀ¸Ä¿ºÍÉÏÊöµÄ Angew. Chem. Int. Ed. Ïàͬ, Ö»ÊDZ¾ÆÚ¿¯ÒÔµÂÎijö°æ (µ«Ã¿ÆÚż¶ûÓм¸ÆªÓ¢ÎÄÎÄÏ×). ÊÇÓÃÀ´Á·Ï°»¯Ñ§µÂÓ¢¶ÔÕÕÔĶÁµÄ»ú»á.
d. Chemische Berichte (µÂ¹ú»¯Ñ§Ñ§±¨): 1868-1945. µÂÎÄÊéд. Ðí¶àÔçÆÚ»¯Ñ§×ÊÁÏÈԵôӱ¾ÆÚ¿¯ÒÔ¼°ÏÂÃæ½éÉÜµÄ Ann. ²éÕÒ.
e. Justus Liebigs Annalen der Chemie (Àû±ÈÏ£»¯Ñ§¼ÍÊÂ), ¼ò³Æ Ann, 1932 Äê³ö°æ, µÂÎÄÊéд, ¿¯ÔØÓлú»¯Ñ§ÓëÉúÎïÓлú·½ÃæµÄÂÛÎÄ. Ŀ¼ÓÐÓ¢µÂ¶ÔÕÕ, ÂÛÎĸ½ÓÐÓ¢ÎÄÕªÒª.
v). ×ۺϿƼ¼·½ÃæµÄÆÚ¿¯: ÒÔÏÂÁ½ÖÖÆÚ¿¯ÊÇËùÓÐÆÚ¿¯Öм¶±ð×î¸ßµÄ, Ó°ÏìÒò×Ó½ÔÔÚ 20 ÒÔÉÏ. ËäȻֻÓб¡±¡¼¸Ò³±¨µ¼, µ«ÒòÊôÓڿƼ¼µÄ´´Ð (·¢Ã÷»ò·¢ÏÖ), ÌØ±ðÊܵ½ÖØÊÓ, Ðí¶à×÷Õß³ÉΪµ±µØ¾ßÓÐÓ°ÏìÁ¦µÄѧÊõ´øÍ·ÈË.
a. Science (¿ÆÑ§): ÃÀ¹ú³ö°æ, Ó°ÏìÒò×Ó 21.9
b. Nature (×ÔÈ»): Ó¢¹ú³ö°æ, 1869 Äê³ö°æ, ÖÜ¿¯, Ó°ÏìÒò×Ó 27.1

        (2). ¹úÄÚ»¯Ñ§ÆÚ¿¯: Óë¹úÍâÆÚ¿¯±È½Ï, ÖйúµÄ»¯Ñ§ÆÚ¿¯À¸Ä¿½Ï¶à¶øÇÒÉú¶¯. ±È½ÏÓÐÃûµÄÆÚ¿¯¶àÓÉÖйú»¯Ñ§»á, ÖпÆÔº, ½ÌÓý²¿»ò¼¸ËùÖØµãѧУÖ÷°ì. ĿǰΪ SCI ÊÕ¼µÄÓл¯Ñ§Ñ§±¨, Öйú»¯Ñ§, ¸ßµÈѧУ»¯Ñ§Ñ§±¨µÈ. ÒÔÓ¢Îijö°æµÄÓÐÖйú»¯Ñ§ (Chinese Journal of Chemistry) ºÍÖйú»¯Ñ§¿ì±¨ (Chinese Chemical Letters) Á½ÖÖ. רÃÅ·¢±íÓлú»¯Ñ§ÁìÓòÂÛÎĵÄÓкϳɻ¯Ñ§, Óлú»¯Ñ§, »¯Ñ§Í¨±¨µÈ. ÒÔϼòÂÔ½éÉܹúÄÚ½ÏÖøÃûµÄ»¯Ñ§ÆÚ¿¯:
        i). ÉϺ£ÓлúËùºÍÖйú»¯Ñ§»áºÏ°ìµÄÈýÖÖ»¯Ñ§ÆÚ¿¯: (2000 Ä꿪ʼ¿ÉÒÔ´ÓÍøÂçÉϲéÔÄ, ÍøÖ·Îª www.sioc.ac.cn/publication)
        a. Óлú»¯Ñ§ (Organic Chemistry): 1980 Äê´´¿¯, רÃű¨µ¼Óлú»¯Ñ§ÁìÓòµÄÂÛÎÄ, °üÀ¨ÓлúºÏ³É, ÉúÎïÓлú, ÎïÀíÓлú, ÌìÈ»Óлú, ½ðÊôÓлúºÍÔªËØÓлúµÈ·½Ãæ. À¸Ä¿Óг¤ÆªµÄ”Ñо¿ÂÛÎÄ”, ¶ÌƪµÄ “Ñо¿Í¨Ñ¶”, “Ñо¿¼ò±¨”.
        b. »¯Ñ§Ñ§±¨ (Acta Chimica Sinica): ¿¯ÔØ×ۺϻ¯Ñ§, °üÀ¨Óлú, ÎÞ»ú, ·ÖÎö, ÎﻯµÈרҵ, À¸Ä¿ÓÐÑо¿×¨Ìâ, Ñо¿ÂÛÎÄ, Ñо¿¼ò±¨. ÌâÄ¿¸½ÓÐͼÎÄÕªÒª·½±ãÁ˽âÎÄÕÂÄÚÈÝ. ±¾ÆÚ¿¯Îª SCI ÊÕ¼³ÉΪ¹ú¼ÊºËÐÄÆÚ¿¯.
        c. Chinese Journal of Chemistry (Öйú»¯Ñ§): ÒÔÓ¢ÎÄÊéд, ±¨µ¼×ۺϻ¯Ñ§, Ϊ SCI ÊÕ¼. ±¾ÆÚ¿¯Ô­Ãû Acta Chimica Sinica English Edition, 1983 Äê´´¿¯, 1990 Äê¸Ä³ÉĿǰÃû³Æ.
  ii). ÖпÆÔº»¯Ñ§ËùºÍÖйú»¯Ñ§»áºÏ°ìµÄÁ½ÖÖ»¯Ñ§ÆÚ¿¯:
a. »¯Ñ§Í¨±¨ (Huaxue Tongbao Chemistry): ÖпÆÔº»¯Ñ§ËùºÍÖйú»¯Ñ§»áÖ÷°ì, 1934 Äê´´¿¯, Ô¿¯, ·¢±íÓлú»¯Ñ§ÁìÓòµÄÂÛÎÄ, À¸Ä¿ÓпÆÑÐÓë̽Ë÷, ¿ÆÑÐÓë½øÕ¹, ʵÑéÓë½Ìѧ, Ñо¿¿ì±¨, ½øÕ¹ÆÀÊö, ֪ʶ½éÉÜ. ÆÚ¿¯ÒÑÉÏÍø, ÍøÖ·Îª: hppt://China.chemistrymag.org
b. Chinese Chemical Letters (Öйú»¯Ñ§¿ì±¨): ÖпÆÔº»¯Ñ§ËùºÍÖйú»¯Ñ§»áÖ÷°ì, ÒÔÓ¢ÎÄÊéд³ö°æ, Ô¿¯, ÄÚÈݼò¶ÌÉú¶¯, 2-4 Ò³.
  iii). ¸ßµÈѧУ»¯Ñ§Ñ§±¨ (Chemical Journal of Chinese University): ½ÌÓý²¿Ö÷°ì, ¼ªÁÖ´óѧ³Ð°ì. 1980 Äê´´¿¯, Ô¿¯. À¸Ä¿ÓÐÑо¿ÂÛÎÄ, Ñо¿¿ì±¨, Ñо¿¼ò±¨. ÿƪÎÄÕºóÃæ¸½ÓÐÓ¢ÎÄÕªÒª. ±¾ÆÚ¿¯Îª SCI ÊÕ¼.
  iv). ±±¾©´óѧѧ±¨ (Acta Scientiarum Naturalium Universitatis Pekinensis) ×ÔÈ»¿ÆÑ§°æ: ±±¾©´óѧ³ö°æ, 1955 Äê´´¿¯, ˫Կ¯. ÄÚÈݺ¬¸ÇËùÓÐ×ÔȻѧ¿Æ (»¯Ñ§, ÎïÀí, ÉúÎï, µØÖÊ, ÊýѧµÈ). À¸Ä¿Óг¤ÆªÂÛÎĺÍÑо¿¼ò±¨.
  v). ´óѧ»¯Ñ§ (University Chemistry): Öйú»¯Ñ§»áºÍ¸ßµÈѧУ½ÌÓýÑо¿ÖÐÐĺϰì. À¸Ä¿ÓнñÈÕ»¯Ñ§, ½ÌѧÑо¿Óë¸Ä¸ï, ֪ʶ½éÉÜ, ¼ÆËã»úÓ뻯ѧ, »¯Ñ§ÊµÑé, ʦÉú±Ê̸, ×Ôѧ֮ÓÑ, »¯Ñ§Ê·, ÊéÆÀ.
  vi). ºÏ³É»¯Ñ§ (Chinese Journal of Synthetic Chemistry): ÖпÆÔº³É¶¼ÓлúËùºÍËÄ´¨Ê¡»¯¹¤Ñ§»áÖ÷°ì, ˫Կ¯, ±¨µ¼Óлú»¯Ñ§ÁìÓòÂÛÎÄ, À¸Ä¿ÓÐÑо¿¿ì±¨, ×ÛÊö, Ñо¿ÂÛÎÄ, Ñо¿¼ò±¨.
  vii). Ó¦Óû¯Ñ§ (Chinese Journal of Applied Chemistry): Öйú»¯Ñ§»áºÍÖпÆÔº³¤´ºÓ¦Óû¯Ñ§Ñо¿ËùºÏ°ì, 1983 Äê´´¿¯, ˫Կ¯. ÄÚÈÝÓÐÑо¿ÂÛÎĺÍÑо¿¼ò±¨, ÎÄÕºóÃæ¸½ÓÐÓ¢ÎÄÕªÒª.
  viii). »¯Ñ§ÊÔ¼Á (Chemical Reagents): »¯¹¤²¿»¯Ñ§ÊÔ¼ÁÐÅÏ¢Õ¾Ö÷°ì, 1979 Äê´´¿¯. À¸Ä¿ÓÐÑо¿±¨¸æÓë¼ò±¨, רÂÛÓë×ÛÊö, ÊÔ¼Á½éÉÜ, ·ÖÎöÔ°µØ, ¾­Ñé½»Á÷, Éú²úÓëÌá´¿¼¼Êõ, ÏûÏ¢.
  ix). ÆäËü: »¯Ñ§ÊÀ½ç, »¯¹¤½øÕ¹, ¾«Ï¸»¯¹¤.
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