Diels-Alder Reactions of Quinol Lactones: A Change of Regioselectivity with Stannic Chloride Catalysis Export

@article{citeulike:281729, abstract = {Lewis acid-mediated Diels-Alder reactions of quinol lactone 2 gave regioselectivity opposite to that of the uncatalyzed reaction. Compound 12 is proposed as the reactive intermediate generated by the reaction of 2 with stannic chloride.}, author = {Kraus, George A. and Cui, Wenge}, citeulike-article-id = {281729}, citeulike-linkout-0 = {http://pubs.acs.org.ezproxy.library.drexel.edu/cgi-bin/article.cgi/joceah/2002/67/i26/html/jo020366p.html/}, day = {5}, editor = {Org and Web}, journal = {Journal of Organic Chemistry}, keywords = {orgo}, month = {December}, number = {26}, pages = {9475--9476}, posted-at = {2005-08-14 21:21:28}, priority = {2}, title = {Diels-Alder Reactions of Quinol Lactones: A Change of Regioselectivity with Stannic Chloride Catalysis}, url = {http://pubs.acs.org.ezproxy.library.drexel.edu/cgi-bin/article.cgi/joceah/2002/67/i26/html/jo020366p.html/}, volume = {67}, year = {2002} }

TY - JOUR ID - citeulike:281729 L3 - citeulike-article-id:281729 N2 - Lewis acid-mediated Diels-Alder reactions of quinol lactone 2 gave regioselectivity opposite to that of the uncatalyzed reaction. Compound 12 is proposed as the reactive intermediate generated by the reaction of 2 with stannic chloride. IS - 26 JF - Journal of Organic Chemistry EP - 9476 TI - Diels-Alder Reactions of Quinol Lactones: A Change of Regioselectivity with Stannic Chloride Catalysis VL - 67 SP - 9475 KW - orgo AU - Kraus, George AU - Cui, Wenge A2 - Org A2 - Web PY - 2002/12/05/ UR - http://pubs.acs.org.ezproxy.library.drexel.edu/cgi-bin/article.cgi/joceah/2002/67/i26/html/jo020366p.html/ ER -